CN1867572B

CN1867572B - Proteasome inhibitors and methods of using the same

Info

Publication number: CN1867572B
Application number: CN2004800301520A
Authority: CN
Inventors: 阿尔贝托·贝尔纳雷吉; 保罗·G·卡萨拉; 桑卡尔·查特吉; 埃德蒙多·费雷蒂; ***·伊克巴勒; 埃内斯托·门塔; 帕特里西亚·A·梅西纳·麦克劳克林; 安布罗焦·奥利娃; 热尔马诺·达拉斯莫; 塞尔吉奥·德·穆纳里; 拉法埃拉·贝尔纳迪尼
Original assignee: Cephalon LLC
Current assignee: Cephalon LLC
Priority date: 2003-08-14
Filing date: 2004-08-13
Publication date: 2012-03-28
Anticipated expiration: 2024-08-13
Also published as: TWI345465B; ZA200601293B; TW200529810A; AR095249A2; PE20050360A1; CN1867572A; AR045381A1; MY162518A; UA88771C2

Abstract

The present invention provides boronic acid compounds, boronic esters, and compositions thereof that can modulate apoptosis such as by inhibition of proteasome activity. The compounds and compositions can be used in methods of inducing apoptosis and treating diseases such as cancer and other disorders associated directly of indirectly with proteasome activity.

Description

Proteasome inhibitor and method of use thereof

Invention field

The present invention relates to effectively as proteasome inhibitor and boric acid and the boric acid ester compound of regulating apoptosis.

Background of invention

Proteasome, (being also referred to as many catalytic proteins enzyme (MCP), many catalytic proteins enzyme, many catalytic proteins enzyme complex, many catalysis endopeptidase mixture, 20S, 26S, or ingensin) are to be present in all eukaryotic tenuigenin and the interior big polyprotein mixture of nuclear.It is the cellularstructure of high conservative, is responsible for the proteolyze (Tanaka, Biochem Biophy.Res.Commun., 1998,247,537) that most cells albumin A TP-relies on.The 26S proteasome is made up of 20S core catalytic complex, and it is added cap at each end by 19S regulation and control subunit.Archeobacteria 20S proteasome contains 14 copies of two kinds of dissimilar subunit α and β, forms the cylindrical-shaped structure of being made up of four rings that pile up.Top and bottom part ring respectively contain 7 α subunits, and inner loop contains 7 β subunits.More complicated eucaryon 20S proteasome is made up of about 15 different 20-30kDa subunits, and is characterized as three the main activity relevant with peptide substrates.For example, it is tryptic that proteasome shows, Quimotrase and peptidyl glutamyl hydrolase polypeptide active (Rivett, Biochem.J., 1993,291,1 and Orlowski, Biochemisty, 1990,29,10289).In addition, proteasome has unique avtive spot mechanism, is considered to utilize threonine residues as catalytic nucleophilic reagent (Seemuller etc., Science, 1995,268,579).

The 26S proteasome can be degraded through adding the albumen that the ubiquitin molecule is labeled.Usually, ubiquitin utilizes ATP to be connected with the epsilon-amino of Methionin with the rapid method of multistep with E2 (ubiquitin combination) enzyme with E1 (ubiquitin activating).The substrate protein of many ubiquitinization is by identification of 26S proteasome and degraded.Usually discharge many ubiquitin chain and ubiquitin is recycled (Goldberg etc., Nature, 1992,357,375) from mixture.

Many modulins are proteoclastic substrates that ubiquitin relies on.Many these albumen play a part the regulatory factor of physiological and pathologic cell process.The change of proteasome activity comprises for example parkinson's disease of nerve retrograde affection with a lot of pathology, and the perfusion damage again of Alzheimer and obstruction/local asphyxia is aging relevant with cns.

Ubiquitin protein enzyme body approach also plays a significant role in tumor growth.Albumen is cyclin for example, the modulated degraded of CDK2 suppressor factor and tumor inhibitor it is believed that for the cell cycle carry out with mitotic division be important.Known protein enzyme body substrate is tumor inhibitor p53, it is relevant with several cell processes (referring to as, Ko, L.J.Genes Dev., 1996,10,1054).Tumor inhibitor p53 has been presented in several hematopoietic cell systems apoptosis-induced (Oren, M., Semin.Cancer Biol., 1994,5,221).Inducing of p53 causes the cell growth to stop at the G1 phase of cell cycle and the necrocytosis that is caused by apoptosis.Tumor inhibitor p53 degraded is known to be carried out through Ubiquitin-Proteasome Pathway, and to destroy the p53 degraded through arrestin enzyme body be apoptosis-induced possible pattern.

Proteasome also be through the degraded transcription factor NF-KB arrestin I κ B make this transcription factor activation needed (Palombella etc., Cell, 1994,78,773).NF-κ B works in keeping cell survival through transcribing inhibitors of apoptosis.Block N F-kB activity has shown makes cell be easier to apoptosis.

Several suppressor factor of proteasome proteolytic activity have been reported.Referring to, for example, Kisselev etc., Chemistry & Biology, 2001,8,739.Lactacystin is the streptomycete metabolite (Fenteany etc., Science, 1995,268,726) of the proteolytic activity of specificity arrestin enzyme nanocrystal composition.This molecule can suppress the propagation (Fenteany etc., Proc.Natl.Acad.Sci.USA, 1994,91,3358) of several cell types.Having shown that lactacystin irreversibly is attached to through its β lactone part is positioned at the aminoterminal threonine residues of proteasome beta subunit.

Chymotrypsin-like active (Vinitsky etc., Biochemistry, 1992,31,9421 that peptide aldehyde has been in the news and has suppressed relevant with proteasome; Tsubuki etc., Biochem.Biophys.Res.Commun., 1993,196,1195; With Rock etc., Cell, 1994,78,761).Reported external IC ₅₀Value is the two peptidyl aldehyde inhibitors of 10-100nM (Iqbal, M. etc., J.Med.Chem.1995,38,2276).A series of same effectively vitro inhibition agent (Iqbal etc., Bioorg.Med.Chem.Lett.1996,6,287, U.S. patents 5,614,649 have also been reported from α-ketone carbonyl and boric acid ester deutero-dipeptides; 5,830,870; 5,990,083; 6,096,778; 6,310,057; U.S. patented claim disclose 2001/0012854 and WO 99/30707).

N-terminal peptide ylboronic acid ester and boronic acid compounds (U.S. patent 4,499,082 and 4,537,773 had been reported in the past; WO 91/13904; Kettner etc., J.Biol.Chem., 1984,259,15106).These compounds are reported as the suppressor factor of some proteolytic ferment.Terminal tripeptides boric acid ester of N-and boronic acid compounds have shown the growth (U.S. patent 5,106,948) of anticancer.Terminal tripeptides boric acid ester of the N-of a large amount of kinds and boronic acid compounds and analogue thereof have shown inhibition feritin (U.S. patent 5,169,841).

The multiple different suppressor factor of proteasome peptidase activity have been reported.Referring to, like Dick etc., Biochemistry, 1991,30,2725; Goldberg etc., Nature, 1992,357,375; Goldberg, Eur.J.Biochem., 1992,203,9; Orlowski, Biochemistry, 1990,29,10289; Rivett etc., Archs.Biochem.Biophys., 1989,218,1; Rivett etc., J.Biol.Chem., 1989,264,12215; Tanaka etc., New Biol., 1992,4,1; Murakami etc., Proc.Natl.Acad Sci.USA, 1986,83,7588; Li etc., Biochemistry, 1991,30,9709; Goldberg, Eur.J.Biochem., 1992,203,9; With Aoyagi etc., proteolytic enzyme and biological regulation and control (Proteases and BiologicalControl), press of cold spring harbor laboratory (1975), pp.429-454.

Stein etc., the U.S. patent application serial number was submitted on March 15th, 08/212,909,1994, and report is effective to reduce the peptide aldehyde of animal muscle mass loss rate and intracellular protein rate of decomposition.This compound it is said and also reduces the proteic degradation rate of animal p53.Palombella etc., WO 95/25533, and report uses peptide aldehyde to reduce cell content and the activity of animal NF-κ B through zooblast is contacted with proteasome function or ubiquitin bonded peptide aldehyde inhibitor.Goldberg and Rock, WO 94/17816, and report uses proteasome inhibitor to suppress the MHC-I antigen presentation.Stein etc., U.S. patent 5,693,617 reports effectively reduce the degradation rate of animal proteinum as the peptidyl aldehyde cpd of proteasome inhibitor.Lum etc., U.S. patent 5,834,487 has reported that 26S and 20S proteasome are suppressed the method for cell proliferation by the inhibition of indone verivate and use indone verivate.Wang etc., U.S. patent 6,075,150 report alpha-keto amide compounds are effectively treated the imbalance of Mammals by the mediation of 20S proteasome.France etc., WO 00/64863, and report uses 2, and 4-diamino--3-alpha-hydroxy carboxylic acid derivatives is as proteasome inhibitor.Yamaguchi etc., EP1166781 report carboxylic acid derivative is as proteasome inhibitor.Ditzel etc., the divalence suppressor factor of EP0995757 report proteasome.Garcia-Echeverria etc., Bioorg.Med.Chem.Lett., the active 2-aminobenzyl of the chymotrypsin-like statin verivate of the non-covalent inhibition of 2001,11,1317 reports 20S proteasome.

Some other proteasome inhibitors comprise the boric acid part.For example, Drexler etc., WO 00/64467, is reported in activated endothelial cells or has among the leukemia cell of high expression level c-myc, contains tetrapeptide boric acid ester and the method for selective induction apoptosis of proteasome inhibitor through use.Furet etc., the proliferative disease that WO 02/096933 report 2-[[N-(2-amino-3-(heteroaryl or aryl) propionyl) aminoacyl] amino]-alkylboronic acids and ester are used to treat warm-blooded animal.U.S. patent 6,083, and 903; 6,297,217; 5,780,454; 6,066,730; 6,297,217; 6,548,668; U.S. patented claim discloses 2002/0173488; Report boric acid ester and boronic acid compounds and the method that is used to reduce the proteolytic degradation rate with WO 96/13266.U.S. patent 6,465, and 433 have also reported the method for using certain boric acid and boric acid ester inhibition virus replication with WO 01/02424.Plamondon etc., the U.S. patented claim discloses 2002/0188100 report boric acid and the new boron trioxide and the pharmaceutically useful compsn of boric acid ester compound.Gardner etc., Biochem.J., 2000,346,447 show that a series of two peptidyls and tripeptides ylboronic acid are the suppressor factor of 20S and 26S proteasome.

Other boracic peptidyls and related compound are reported in U.S. patent 5,250,720; 5,242,904; 5,187,157; 5,159,060; 5,106,948; 4,963,655; 4,499,082; With WO 89/09225, WO/98/17679, WO 98/22496, and WO 00/66557; WO 02/059130, and WO 03/15706, and WO 96/12499, and WO 95/20603; WO 95/09838, and WO 94/25051, and WO 94/25049, and WO 94/04653; WO 02/08187, EP632026, and EP354522.

Shown in above-mentioned reference, for very big interest being arranged the active medicine of modulin enzyme body.For example can the active molecule of arrestin enzyme body can end or delay cancer progression through the orderly degraded of interference cell cyclin or tumor inhibitor.Therefore, new and/or improved proteasome inhibitor there is lasting demand.

Summary of the invention

The present invention relates to effectively be used as the new boric acid and the boric acid ester compound of proteasome inhibitor and modulating apoptosis.The present invention also comprises the many catalytic proteins enzyme (" MCP ") that suppresses relevant with some imbalance, comprises the method for treatment amyotrophy imbalance (wasting disorder).

In one embodiment, the have formula compound of (I) is provided:

Wherein integral part and preferred integral part define hereinafter.

In another embodiment, the present invention provides the compound that contains general formula (I) and the pharmaceutical composition of pharmaceutically acceptable carrier.

In another embodiment, the present invention provides arrestin enzyme body active method, comprises that the compound with general formula (I) contacts with said proteasome.

In another embodiment, the present invention provides the treatment method for cancer, comprises having or tend to have the compound of general formula (I) of the Mammals drug treatment significant quantity of said cancer.

In another embodiment, the present invention provides the treatment method for cancer, comprises that wherein said cancer is selected from skin carcinoma to having or tend to have the compound of general formula (I) of the Mammals drug treatment significant quantity of said cancer; Prostate cancer, colorectal carcinoma, carcinoma of the pancreas, kidney; Ovarian cancer, mammary cancer, liver cancer; Tongue cancer, lung cancer and smooth muscle tissue's cancer.

In another embodiment; The present invention provides the treatment method for cancer, comprises that wherein said cancer is selected from white blood disease to having or tend to have the compound of general formula (I) of the Mammals drug treatment significant quantity of said cancer; Lymphoma; Non--He Jiejin lymphomas, myelomatosis, and multiple myeloma.

In another embodiment; The present invention provides the treatment method for cancer; Comprise having or tend to have the compound of general formula (I) of the Mammals drug treatment significant quantity of said cancer, and combine one or more antitumor or carcinostatic agent and/or radiotherapy.

In another embodiment, the present invention provides a kind of inhibition transcription factor NF-KB active method, comprises that the suppressor factor I κ B with transcription factor NF-KB contacts with the compound of general formula (I).

In another embodiment, the compound of the present invention's general formula (I) of being provided for treating.

In another embodiment, the present invention provides the application of compound in the medicine of production for treating cancer of general formula (I).

In another embodiment, the present invention provides the method for preparing formula (II) compound:

Wherein integral part defines at this, through type (II-b) glycol:

Suitable tri-alkoxy borine with formula (II-a):

Wherein integral part defines at this; Under the condition that is suitable for the formula that forms (II-c) midbody, react for some time:

And under the condition that is suitable for the formula that forms (II) compound, make formula (II-c) midbody or and i) formula R ¹CH ₂MX ^HalReagent react, wherein M is a metal, and X ^HalBe halogen atom, or with ii) formula R ¹CH ₂Li reagent react for some time.

These of this compound and other characteristic will the form with expansion be set forth with continuing disclosed content.

The invention embodiment is described

The present invention especially provides arrestin enzyme body activity and is used to treat the disease relevant with proteasome activity or the compound of imbalance.Compound of the present invention comprises formula (I) compound,

Or its pharmacologically acceptable salt, steric isomer or tautomer form, wherein:

R ¹Be C ₁-C ₈Alkyl, C ₂-C ₈Thiazolinyl, C ₂-C ₈Alkynyl, or C ₃-C ₇Naphthenic base;

R ²Be H ,-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y ,-(CH ₂) _bCH ₂CONR ⁵R ⁶,-(CH ₂) _cCH ₂N (R ⁴) CONH ₂,-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰, or-(CH ₂) _eCH (R ⁷) ZR ⁸

A, b and c are 0,1,2,3,4,5 independently of one another, or 6;

D and e are 0,1,2,3 independently of one another, or 4;

R ⁴Be H or C ₁-C ₁₀Alkyl;

R ⁵And R ⁶Be H independently of one another, C ₁-C ₁₀Alkyl, carbocylic radical, assorted carbocylic radical, or amino protecting group;

Perhaps, R ⁵And R ⁶The N atom that is connected with them forms assorted carbocylic radical altogether;

R ⁷Be H or C ₁-C ₁₀Alkyl;

R ⁸Be H, C ₁-C ₁₀Alkyl, alkyl-S (=O) ₂-, aryl-S (O) ₂-, H ₂NS (=O) ₂-,-SO ₃H, or protection base;

R ⁹Be H, C ₁-C ₁₀Alkyl, carbocylic radical, or assorted carbocylic radical;

R ¹⁰Be H, C ₁-C ₁₀Alkyl, carbocylic radical, assorted carbocylic radical, C ₁-C ₁₀Alkyl-C (=O)-, C ₂-C ₁₀Thiazolinyl-C (=O)-, C ₂-C ₁₀Alkynyl-C (=O)-, carbocylic radical-C (=O)-, assorted carbocylic radical-C (=O)-, carbocylic radical alkyl-C (=O)-, assorted carbocylic radical alkyl-C (=O)-, C ₁-C ₁₀Alkyl-S (=O) ₂-, carbocylic radical-S (=O) ₂-, assorted carbocylic radical-S (=O) ₂-, carbocylic radical alkyl-S (=O) ₂-, assorted carbocylic radical alkyl-S (=O) ₂-, C ₁-C ₁₀Alkyl-NHC (=O)-, carbocylic radical-NHC (=O)-, assorted carbocylic radical-NHC (=O)-, carbocylic radical alkyl-NHC (=O)-, assorted carbocylic radical alkyl-NHC (=O)-, C ₁-C ₁₀Alkyl-OC (=O)-, carbocylic radical-OC (=O)-, assorted carbocylic radical-OC (=O)-, carbocylic radical alkyl-OC (=O)-, assorted carbocylic radical alkyl-OC (=O)-, C ₁-C ₁₀Alkyl-NH-C (=O)-NHS (=O) ₂-, carbocylic radical-NH-C (=O)-NHS (=O) ₂-, assorted carbocylic radical-NH-C (=O)-NHS (=O) ₂-, C ₁-C ₁₀Alkyl-S (=O) ₂-NH-C (=O)-, carbocylic radical-S (=O) ₂-NH-C (==O)-, assorted carbocylic radical-S (=O) ₂-NH-C (=O)-, or amino protecting group;

R wherein ¹⁰The optional replacement with 1,2 or 3R ²³

Perhaps, R ⁹And R ¹⁰The N atom that connects with their forms optional the replacement with 1,2 or 3R ²³Assorted carbocylic radical,

Y is H ,-CN ,-NO ₂,-S (=O) ₂R ¹¹, or guanidine radicals protection base;

R ¹¹Be C ₁-C ₆Alkyl, aryl, or NR ¹²R ¹³

R ¹²And R ¹³Be H independently, C ₁-C ₁₀Alkyl, carbocylic radical, assorted carbocylic radical, or amino protecting group;

Perhaps, R ¹²And R ¹³The N atom that connects with them forms assorted carbocylic radical;

Z is O, S, Se, or Te;

Q is-B (OH) ₂,-B (OR ¹⁴) ₂, or the ring-type boric acid ester, wherein said ring-type boric acid ester contains 2-20 carbon atom, and optional heteroatoms N, S, or O;

R ¹⁴Be H, C ₁-C ₄Alkyl, naphthenic base, cycloalkylalkyl, aryl, or aralkyl;

X is R ^AC (=O)-, R ^ANHC (=O), R ^AS (=O) ₂-, R ^AOC (=O)-, R ^ASC (=O)-, or R ^A

R ^ABe C ₁-C ₂₀Alkyl, the optional replacement with R ²⁰

C ₂-C ₂₀Thiazolinyl, the optional replacement with R ²⁰

C ₂-C ₂₀Alkynyl, the optional replacement with R ²⁰

Carbocylic radical, the optional replacement with 1-5R ²¹Or

Assorted carbocylic radical, the optional replacement with 1-5R ²¹

R ²⁰Be selected from:

-CN, halogen, haloalkyl-, C ₁-C ₄Alkyl, C ₂-C ₄Thiazolinyl, C ₂-C ₄Alkynyl ,-CO ₂H ,-C (=O) CO ₂H ,-C (=O) NH ₂,-C (=O) H ,-S (=O) NH ₂,-S (=O) ₂NH ₂,-OH ,-SH ,-NH ₂,-NH (alkyl) ,-N (alkyl) ₂,-NHC (=O) NH ₂,-NHC (=O) R ^20a,-NHC (=O) OR ^20a,-OR ^20a,-SR ^20a,-S (=O) R ^20a,-S (=O) ₂R ^20a,-S (=O) ₂-NHR ^20a,-SC (=O) R ^20a,-C (=O) R ^20a,-C (=O) NHR ^20a,-C (=O) O-R ^20a,-NHS (=O) ₂R ^20a,-NHR ^20b, phthalimido ,-(O-alkyl) _r-OH ,-(O-alkyl) _r-(O-alkyl) ,-OR ^20c,-SR ^20c,-O-alkyl-R ^20c,-S-alkyl-R ^20c,-S (=O)-R ^20c,-S (=O) ₂-R ^20c,-S (=O) ₂-NHR ^20c,-SC (=O) R ^20c,-C (=O) R ^20c,-C (=O) OR ^20c,-C (=O) NHR ^20c, the optional replacement with 1-5R ²¹Carbocylic radical; Replace with 1-5R with optional ²¹Assorted carbocylic radical;

R ^20aBe C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, or C ₂-C ₂₀Alkynyl; Wherein said alkyl, thiazolinyl, or alkynyl is optional by one or more halogens, OH, CN, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₂-C ₈The alkoxyl group alkoxyl group, aryl, heteroaryl, or-NHR ^20bReplace;

R ^20bIt is amino protecting group;

R ^20cBe carbocylic radical, the optional replacement with 1-5R ²²Or

Assorted carbocylic radical, the optional replacement with 1-5R ²²

R ²¹Be selected from:

C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl ,-OR ^21a,-SR ^21a,-CN, halogen, haloalkyl ,-NH ₂,-NH (alkyl) ,-N (alkyl) ₂,-NHC (=O) O-alkyl ,-NHC (=O) alkyl ,-COOH ,-C (=O) O-alkyl ,-C (=O) alkyl ,-C (O) H ,-S (=O)-alkyl ,-S (=O) ₂-alkyl ,-S (=O)-aryl ,-S (=O) ₂-aryl, optional with 1-5R ²²Substituted carbocylic radical, and optional with 1-5R ²²Substituted assorted carbocylic radical;

R ^21aBe H, C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, carbocylic radical, or assorted carbocylic radical;

R ²²Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, phenyl, halogen, haloalkyl, alkoxyl group; Thio alkoxy (thialkoxy), amino, alkylamino, dialkyl amido, carboxyl; Alkyl-OC (=O)-, alkyl-C (=O)-, aryl-OC (=O)-, alkyl-OC (=O) NH-; Aryl-OC (=O) NH-, alkyl-C (=O) NH-, alkyl-C (=O) O-, (alkyl-O) _r-alkyl, and HO-(alkyl-O) _r-alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, alkyl-S (=O)-, alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-;

R ²³Be selected from:

C ₁-C ₆Alkyl, C ₂-C ₆Thiazolinyl, C ₂-C ₆Alkynyl, F, Cl, Br, I, haloalkyl ,-NH ₂,-NHR ^23a,-N (R ^23a) ₂,-N ₃,-NO ₂,-CN ,-CNO ,-CNS ,-C (=O) OR ^23a,-C (=O) R ^23a,-OC (=O) R ^23a-N (R ^23a) C (=O) R ^23a,-N (R ^23a) C (=O) OR ^23a,-C (=O) N (R ^23a) ₂, urea groups ,-OR ^23a,-SR ^23a,-S (=O)-(C ₁-C ₆Alkyl) ,-S (=O) ₂-(C ₁-C ₆Alkyl) ,-S (=O)-aryl ,-S (=O) ₂-aryl ,-S (=O) ₂-N (R ^23a) ₂

With 1-5R ²⁴Optional substituted carbocylic radical; With with 1-5R ²⁴Substituted assorted carbocylic radical;

R ^23aBe H or C ₁-C ₆Alkyl;

Perhaps, two R ^23aThe N atom that can be connected with them is combined and is formed 5-7 element heterocycle base; With

R ²⁴Be selected from:

C ₁-C ₄Alkyl, C ₂-C ₄Thiazolinyl, C ₂-C ₄Alkynyl, phenyl, halogen, haloalkyl, alkoxyl group; Thio alkoxy, amino, alkylamino, dialkyl amido, carboxyl; Alkyl-OC (=O)-, alkyl-C (=O)-, aryl-OC (=O)-, alkyl-OC (=O) NH-; Aryl-OC (=O) NH-, alkyl-C (=O) NH-, alkyl-C (=O) O-, (alkyl-O) _r-alkyl, and HO-(alkyl-O) _r-alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, alkyl-S (=O)-, alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-; And

R is 1,2,3,4,5,6,7,8,9, or 10;

Condition is, when Q is 1,1,2, during 2-tetramethylethylene glycol boric acid ester, X is not the aralkyl oxy carbonyl;

Condition is, when Q is 1,1,2, and 2-tetramethylethylene glycol boric acid ester, and R ¹When being naphthenic base, R ²Be not-CH ₂CONH ₂With

Condition is, when X is R ^AC (=O)-, R ^ABe with R ²⁰Substituted C ₄-C ₁₅Straight chained alkyl,

And R ²⁰Be-CN-CO ₂H ,-C (=O) O-R ^20a,-NHS (=O) ₂R ^20a,-NHC (=O) R ^20a,-NHR ^20b, or during phthalimido; R ²Be not-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y,

Wherein Y is H ,-CN ,-NO ₂, or guanidine radicals protection base.

In further embodiment, work as R ²Be-(CH ₂) _eCH (R ⁷) ZR ⁸, e is 0, R ⁷Be H, R ⁸Be C ₁-C ₁₀Alkyl and X are R ^AC (=O)-time, R then ^ABe not aminoalkyl group-, the alkylamino alkyl-, dialkyl aminoalkyl-, or urea groups alkyl-.

In some embodiments, R ¹Be C ₁-C ₄Alkyl, and in further embodiment, R ¹Be propyl group, such as the 2-propyl group.

In some embodiments, R ²Be-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y ,-(CH ₂) _bCH ₂CONR ⁵R ⁶,-(CH ₂) _cCH ₂N (R ⁴) CONH ₂,-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰, or-(CH ₂) _eCH (R ⁷) ZR ⁸

In some embodiments, R ²Be-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y and a be 1,2,3,4, or 5.

In some embodiments, R ²Be-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y and a be 2.

In some embodiments, R ²Be-CH ₂CH ₂CH ₂NHC (=NR ⁴) NH-Y.

In some embodiments, R ²Be-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰With d be 0,1, or 2.

In some embodiments, R ²Be-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰With d be 0.

In some embodiments, R ²Be-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰And R ⁹Be H.

In some embodiments, R ²Be-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰

In some embodiments, R ²Be-CH (R ⁷) NR ⁹R ¹⁰

In some embodiments, R ²Be-CH ₂NH-C (=O) OCH ₂(C ₆H ₅).

In some embodiments, R ²Be-(CH ₂) _eCH (R ⁷) ZR ⁸With e be 0,1, or 2.

In some embodiments, R ²Be-(CH ₂) _eCH (R ⁷) ZR ⁸With e be 0.

In some embodiments, R ²Be-(CH ₂) _eCH (R ⁷) ZR ⁸

In some embodiments, R ²Be-CH (R ⁷) ZR ⁸

In further embodiment, Z is O.

In further embodiment, Q has formula (II-a):

D wherein, R ^15a, R ^15b, R ^15c, R ^15d, p and q definition are as follows.

In further embodiment, Q is B (OH) ₂Or the ring-type boric acid ester, wherein said ring-type boric acid ester contains 6-10 carbon atom and contains at least one cycloalkyl moiety.

In further embodiment, Q is B (OH) ₂

In further embodiment, Q is the pinine glycol boric acid ester.

In further embodiment, Q be dicyclohexyl-1,1 '-glycol borate ester.

In further embodiment, Q is 1,2-dicyclohexyl-ethane-1,2-glycol borate ester.

Perhaps, in some embodiments, Q is-B (OH) ₂,-B (OR ¹⁴) ₂,

and

Wherein: R ¹⁴, R ^15a, R ^15b, R ^15c, R ^Lsd, W, W ¹, p and q definition are as follows.

In further embodiment, Q is:

and

W replaces or unsubstituted C ₄-C ₁₀Cycloalkyl ring.

In some embodiments, X is R ^AC (=O)-.

In some embodiments, X is R ^ANHC (=O)-.

In some embodiments, X is R ^AS (O) ₂-.

In some embodiments, R ^ABy-(O-alkyl) _r-OH or-(O-alkyl) _rThe substituted C of-(O-alkyl) ₁-C ₁₄Alkyl, wherein r is 1,2,3,4, or 5.

In some embodiments, R ^ABy-(O-alkyl) _r-OH or-(O-alkyl) _rThe substituted C of-(O-alkyl) ₁-C ₁₄Alkyl, wherein r is 1,2, or 3.

In some embodiments, R ^AComprise at least one-CH ₂CH ₂The O-group.

In some embodiments, R ^ABe-CH ₂(OCH ₂CH ₂) _rOCH ₃

In some embodiments, R ^ABe-CH ₂OCH ₂CH ₂OCH ₂CH ₂OCH ₃Or-CH ₂OCH ₂CH ₂OCH ₃

In some embodiments, R ^AIt is optional respectively the replacement with 1-5R ²¹Aryl or heteroaryl.

In some embodiments, R ^AIt is optional respectively the replacement with 1-5R ²¹Naphthenic base or Heterocyclylalkyl.

In some embodiments, R ^ABe C ₁-C ₂₀Alkyl; C ₂-C ₂₀Thiazolinyl; Or C ₂-C ₂₀Alkynyl, optional respectively the replacement with R ²⁰

In some embodiments, R ^ABe C ₁-C ₂₀Alkyl; C ₂-C ₂₀Thiazolinyl; Or C ₂-C ₂₀Alkynyl, optional respectively the replacement with carbocylic radical or assorted carbocylic radical,, wherein said carbocylic radical or assorted carbocylic radical be optional to be replaced with 1,2 or 3R ²¹

In some embodiments, R ^ABe C ₁-C ₂₀Alkyl; C ₂-C ₂₀Thiazolinyl; Or C ₂-C ₂₀Alkynyl, optional respectively the replacement with aryl,, wherein said aryl is optional to be replaced with 1,2 or 3R ²¹

In some embodiments, R ^ABe C ₁-C ₂₀Alkyl; C ₂-C ₂₀Thiazolinyl; Or C ₂-C ₂₀Alkynyl, optional respectively the replacement with heteroaryl,, wherein said heteroaryl is optional to be replaced with 1,2 or 3R ²¹

In some embodiments, R ^ABe C ₁-C ₂₀Alkyl; C ₂-C ₂₀Thiazolinyl; Or C ₂-C ₂₀Alkynyl, optional respectively the replacement with naphthenic base,, wherein said naphthenic base is optional to be replaced with 1,2 or 3R ²¹

In some embodiments, R ^ABe C ₁-C ₂₀Alkyl; C ₂-C ₂₀Thiazolinyl; Or C ₂-C ₂₀Alkynyl, optional respectively the replacement with Heterocyclylalkyl,, wherein said Heterocyclylalkyl is optional to be replaced with 1,2 or 3R ²¹

In some embodiments, R ^ABe C ₁-C ₂₀Alkyl; C ₂-C ₂₀Thiazolinyl; Or C ₂-C ₂₀Alkynyl, optional respectively the replacement with R ²⁰, R wherein ²⁰Be selected from CN, halogen, haloalkyl ,-CO ₂H ,-C (=O) CO ₂H ,-C (=O) NH ₂,-C (=O) H ,-S (O) NH ₂,-S (O) ₂NH ₂,-OH ,-SH ,-NH ₂,-NH (alkyl) ,-N (alkyl) ₂,-NHC (=O) NH ₂,-NHC (=O) R ^20a,-NHC (=O) OR ^20a,-OR ^20a,-SR ^20a,-S (O) R ^20a,-S (O) ₂R ^20a,-S (O) ₂-NHR ^20a,-SC (=O) R ^20a,-C (=O) R ^20a,-C (=O) NHR ^20a,-C (=O) O-R ^20a,-NHS (O) ₂R ^20a,-NHR ^20b, phthalimido ,-(O-alkyl) ,-(O-alkyl) _r-OH ,-(O-alkyl) _r-(O-alkyl) ,-OR ^20c,-SR ^20c,-O-alkyl-R ^20c,-S-alkyl-R ^20c,-S (O)-R ^20c,-S (O) ₂-R ^20c,-S (O) ₂-NHR ^20c,-SC (=O) R ^20c,-C (=O) R ^20c,-C (=O) OR ^20cAnd-C (=O) NHR ^20c

In some embodiments, R ²Be that H and X are (O-alkyl)-(O-alkyl) _r-(C ₁-C ₁₄Alkyl)-C (=O)-or HO-(alkyl-O) _r-(C ₁-C ₁₄Alkyl)-C (=O)-.

In some embodiments, X is R ^AC (=O)-and R ^ABe C ₄-C ₁₆Alkyl.

In some embodiments, X is R ^AC (=O)-and R ^AIt is optional the replacement with 1-3R ²¹Aryl.

In some embodiments, X is R ^AC (=O)-and R ^AIt is optional the replacement with 1-3R ²¹Assorted carbocylic radical.

In some embodiments, X is R ^AC (=O)-; R ^ABe to replace with 1 R ²¹Phenyl; And R ²¹It is phenoxy.

In some embodiments, X is R ^AC (=O)-, R ^ABe to replace with R ²⁰C ₁-C ₄Alkyl, and R ²⁰It is optional the replacement with 1-3R ²¹Aryl; And in further embodiment, aryl is replaced by at least one halogen.

In some embodiments, X is R ^AC (=O)-; R ^ABe to replace with R ²⁰C ₁-C ₁₄Alkyl; And R ²⁰Be-OR ^20aOr-OR ^20c

In some embodiments, X is R ^AC (=O)-; R ^ABe to replace with R ²⁰C ₁-C ₁₄Alkyl; And R ²⁰It is optional the replacement with 1-3R ²¹Assorted carbocylic radical.

In some embodiments, X is R ^AS (O) ₂-and R ^ABe C ₃-C ₁₆Alkyl.

In some embodiments, the present invention provides formula (I) compound or pharmaceutically acceptable salt thereof form,

Wherein stereochemistry belongs to formula (I-s):

In some embodiments, the present invention provides formula (I) compound,

A, b and c are 0,1,2,3,4,5 independently of one another, or 6;

D and e are 0,1,2,3 independently of one another, or 4;

R ⁴Be H or C ₁-C ₁₀Alkyl;

R ⁷Be H or C ₁-C ₁₀Alkyl;

R ¹⁰Be H, C ₁-C ₁₀Alkyl, carbocylic radical, assorted carbocylic radical, C ₁-C ₁₀Alkyl-C (=O)-, carbocylic radical-C (=O)-, assorted carbocylic radical-C (=O)-, carbocylic radical alkyl-C (=O)-, assorted carbocylic radical alkyl-C (=O)-, C ₁-C ₁₀Alkyl-S (=O) ₂-, carbocylic radical-S (=O) ₂-, assorted carbocylic radical-S (=O) ₂-, carbocylic radical alkyl-S (=O) ₂-, assorted carbocylic radical alkyl-S (=O) ₂-, C ₁-C ₁₀Alkyl-NHC (=O)-, carbocylic radical-NHC (=O)-, assorted carbocylic radical-NHC (=O)-, carbocylic radical alkyl-NHC (=O)-, assorted carbocylic radical alkyl-NHC (=O)-, C ₁-C ₁₀Alkyl-OC (=O)-, carbocylic radical-OC (=O)-, assorted carbocylic radical-OC (=O)-, carbocylic radical alkyl-OC (=O)-, assorted carbocylic radical alkyl-OC (=O)-, or amino protecting group; R wherein ¹⁰The optional replacement with 1,2 or 3R ²³

Perhaps, R ⁹And R ¹⁰The N atom that connects with them forms assorted carbocylic radical;

Y is H ,-CN ,-NO ₂,-S (=O) ₂R ¹¹, or guanidine radicals protection base;

R ¹¹Be C ₁-C ₆Alkyl, aryl, or NR ¹²R ¹³

Z is O, S, Se, or Te;

R ^ABe C ₁-C ₂₀Alkyl, the optional replacement with R ²⁰

C ₂-C ₂₀Thiazolinyl, the optional replacement with R ²⁰

C ₂-C ₂₀Alkynyl, the optional replacement with R ²⁰

Carbocylic radical, the optional replacement with 1-5R ²¹Or

Assorted carbocylic radical, the optional replacement with 1-5R ²¹

R ²⁰Be selected from:

-CN, halogen, haloalkyl-, C ₁-C ₄Alkyl, C ₂-C ₄Thiazolinyl, C ₂-C ₄Alkynyl ,-CO ₂H ,-C (=O) CO ₂H ,-C (=O) NH ₂,-C (=O) H ,-S (=O) NH ₂,-S (=O) ₂NH ₂,-OH ,-SH ,-NH ₂,-NH (alkyl) ,-N (alkyl) ₂,-NHC (=O) NH ₂,-NHC (=O) R ^20a,-NHC (=O) OR ^20a,-OR ^20a,-SR ^20a,-S (=O) R ^20a,-S (=O) ₂R ^20a,-S (=O) ₂-NHR ^20a,-SC (=O) R ^20a,-C (=O) R ^20a,-C (=O) NHR ^20a,-C (=O) O-R ^20a,-NHS (=O) ₂R ^20a,-NHR ^20b, phthalimido ,-(O-alkyl) _r,-O-alkyl-OH ,-(O-alkyl) _r-OH ,-OR ^20c,-SR ^20c,-O-alkyl-R ^20c,-S-alkyl-R ^20c,-S (=O)-R ^20c,-S (=O) ₂-R ^20c,-S (=O) ₂-NHR ^20c,-SC (=O) R ^20c,-C (=O) R ^20c,-C (=O) OR ^20c,-C (=O) NHR ^20c, the optional replacement with 1-5R ²¹Carbocylic radical; Replace with 1-5R with optional ²¹Assorted carbocylic radical;

R ^20aBe C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, or C ₂-C ₂₀Alkynyl; Wherein said alkyl, thiazolinyl, or alkynyl is optional by one or more halogens, C ₁-C ₄Alkyl, aryl, heteroaryl, or-NHR ^20bReplace;

R ^20bIt is amino protecting group;

R ^20cBe carbocylic radical, the optional replacement with 1-5R ²²Or

Assorted carbocylic radical, the optional replacement with 1-5R ²²

R ²¹Be selected from:

C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, C ₁-C ₂₀Alkoxyl group, C ₁-C ₂₀Thio alkoxy ,-OH ,-CN, halogen, haloalkyl ,-NH ₂,-NH (alkyl) ,-N (alkyl) ₂,-NHC (=O) O-alkyl ,-NHC (=O) alkyl ,-C (=O) O-alkyl ,-C (=O) alkyl ,-S (=O)-alkyl ,-S (=O) ₂-alkyl ,-S (=O)-aryl ,-S (=O) ₂-aryl, optional with 1-5R ²²Substituted carbocylic radical; And it is optional with 1-5R ²²Substituted assorted carbocylic radical;

R ²²Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, phenyl, halogen, haloalkyl, alkoxyl group; Thio alkoxy, amino, alkylamino, dialkyl amido, carboxyl; Alkyl-OC (=O)-, alkyl-C (=O)-, aryl-OC (=O)-, alkyl-OC (=O) NH-; Aryl-OC (=O) NH-, alkyl-C (=O) NH-, alkyl-C (=O) O-, (alkyl-O) _r-alkyl, and HO-(alkyl-O) _r-alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, alkyl-S (=O)-, alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-;

R ²³Be selected from:

C ₁-C ₆Alkyl, C ₂-C ₆Thiazolinyl, C ₂-C ₆Alkynyl, F, Cl, Br, I, haloalkyl ,-NH ₂,-NHR ^23a,-N (R ^23a) ₂,-N ₃,-NO ₂,-CN ,-CNO ,-CNS ,-C (=O) OR ^23a,-C (=O) R ^23a,-OC (=O) R ^23a,-N (R ^23a) C (=O) R ^23a,-C (=O) N (R ^23a) ₂, urea groups ,-OR ^23a,-SR ^23a,-S (=O) ₂-(C ₁-C ₆Alkyl) ,-S (=O) ₂-aryl and-S (=O) ₂-N (R ^23a) ₂

R ^23aBe H or C ₁-C ₆Alkyl;

R is 2,3,4,5,6,7,8,9, or 10; And

Condition is, when X is R ^AC (=O)-, R ^ABe with R ²⁰Substituted C ₄-C ₁₅Straight chained alkyl, and R ²⁰Be-CN-CO ₂H ,-C (=O) O-R ^20a,-NHS (=O) ₂R ^20a,-NHC (=O) R ^20a,-NHR ^20b, or during phthalimido; R ²Be not-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y, wherein Y is H ,-CN ,-NO ₂, or guanidine radicals protection base.

In some embodiments, R ¹It is the 2-propyl group; R ²Be H ,-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y ,-(CH ₂) _bCH ₂CONR ⁵R ⁶,-(CH ₂) _cCH ₂N (R ⁴) CONH ₂,-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰, or-(CH ₂) _eCH (R ⁷) ZR ⁸Q is-B (OH) ₂Or pinine glycol boric acid ester; X is R ^AC (=O)-; And R ^ABe C ₄-C ₁₆Alkyl; The optional replacement with 1-3R ²¹Aryl; Or optional the replacement with 1-3R ²¹Assorted carbocylic radical.

In some embodiments, the present invention provides formula (I) compound,

R ¹Be C ₁-C ₈Alkyl;

R ²Be-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y ,-(CH ₂) _cCH ₂N (R ⁴) CONH ₂,-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰, or-(CH ₂) _eCH (R ⁷) ZR ⁸

A is 1,2,3,4, or 5;

C is 1,2,3,4, or 5;

D is 0,1, or 2;

E is 0,1, or 2;

R ⁷Be H or methyl;

R ⁸Be H, C ₁-C ₁₀Alkyl ,-S (=O) ₂-alkyl ,-S (O) ₂-aryl ,-S (=O) ₂-NH ₂,-SO ₃H, or protection base;

Y is H ,-CN ,-NO ₂,-S (=O) ₂R ¹¹, or guanidine radicals protection base;

Perhaps, R ⁹And R ¹⁰The N atom that connects with them forms assorted carbocylic radical,

R ¹¹Be C ₁-C ₆Alkyl, aryl, or NR ¹²R ¹³

Z is O or S;

Q is-B (OH) ₂,-B (OR ¹⁴) ₂, or the ring-type boric acid ester, wherein said ring-type boric acid ester contains 6-20 carbon atom, and contains at least one cycloalkyl moiety;

R ¹⁴Be H, C ₁-C ₄Alkyl, or naphthenic base;

R ^ABe C ₁-C ₂₀Alkyl, the optional replacement with R ²⁰

C ₂-C ₂₀Thiazolinyl, the optional replacement with R ²⁰

C ₂-C ₂₀Alkynyl, the optional replacement with R ²⁰

Carbocylic radical, the optional replacement with 1-5R ²¹Or

Assorted carbocylic radical, the optional replacement with 1-5R ²¹

R ²⁰Be selected from:

R ^20bIt is amino protecting group;

R ^20cBe carbocylic radical, the optional replacement with 1-5R ²²Or

Assorted carbocylic radical, the optional replacement with 1-5R ²²

R ²¹Be selected from:

R ²²Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₁₀Thiazolinyl, C ₂-C ₁₀Alkynyl, phenyl, halogen, haloalkyl, alkoxyl group; Thio alkoxy, amino, alkylamino, dialkyl amido, carboxyl; Alkyl-OC (=O)-, alkyl-C (=O)-, aryl-OC (=O)-, alkyl-OC (=O) NH-; Aryl-OC (=O) NH-, alkyl-C (=O) NH-, alkyl-C (=O) O-, (alkyl-O) _r-alkyl, and HO-(alkyl-O) _r-alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, alkyl-S (=O)-, alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-;

R ²³Be selected from:

R ^23aBe H or C ₁-C ₆Alkyl;

R is 2,3,4,5,6,7,8,9, or 10;

In further embodiment, the present invention provides formula (I) compound,

R ¹Be C ₁-C ₄Alkyl;

R ²Be-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y ,-(CH ₂) _cCH ₂NHCONH ₂, or-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰

A is 1,2, or 3;

C is 1,2, or 3;

D is 0, or 1;

R ⁷Be H or methyl;

R ⁹Be H, or C ₁-C ₁₀Alkyl;

R ¹⁰Be H, C ₁-C ₁₀Alkyl, or amino protecting group;

Y is H ,-CN, or-NO ₂

Q is-B (OH) ₂, the pinine glycol boric acid ester, dicyclohexyl-1,1 '-glycol borate ester, or 1,2-dicyclohexyl-ethane-1,2-glycol borate ester;

R ^ABe C ₁-C ₂₀Alkyl, the optional replacement with R ²⁰

C ₂-C ₂₀Thiazolinyl, the optional replacement with R ²⁰

C ₂-C ₂₀Alkynyl, the optional replacement with R ²⁰

Carbocylic radical, the optional replacement with 1-5R ²¹Or

Assorted carbocylic radical, the optional replacement with 1-5R ²¹

R ²⁰Be selected from:

R ^20bIt is amino protecting group;

R ^20cBe carbocylic radical, the optional replacement with 1-5R ²²Or

Assorted carbocylic radical, the optional replacement with 1-5R ²²

R ²¹Be selected from:

R ²²Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₁₀Thiazolinyl, C ₂-C ₁₀Alkynyl, phenyl, halogen, haloalkyl, alkoxyl group; Thio alkoxy, amino, alkylamino, dialkyl amido, carboxyl; Alkyl-OC (=O)-, alkyl-C (=O)-, aryl-OC (=O)-, alkyl-OC (=O) NH-; Aryl-OC (=O) NH-, alkyl-C (=O) NH-, alkyl-C (=O) O-, (alkyl-O) _r-alkyl, and HO-(alkyl-O) _r-alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, alkyl-S (=O)-, alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-; And

R is 2,3,4, or 5;

Condition is, when X is R ^AC (=O)-, R ^ABe with R ²⁰Substituted C ₄-C ₁₅Straight chained alkyl, and R ²⁰Be-CN-CO ₂H ,-C (=O) O-R ^20a,-NHS (=O) ₂R ^20a,-NHC (=O) R ^20a,-NHR ^20b, or during phthalimido; R ²Be not-(CH ₂) _aCH ₂NHC (=NR ⁴) NH-Y, wherein Y is H ,-CN, or-NO ₂

In further embodiment, the present invention provides formula (I) compound or pharmaceutically acceptable salt thereof, steric isomer or tautomer form, wherein:

R ¹Be C ₁-C ₆Alkyl, C ₂-C ₆Thiazolinyl, C ₂-C ₆Alkynyl, or C ₃-C ₇Naphthenic base;

R ²Be-CH ₂NH ₂, or-CH ₂NR ⁹R ¹⁰

R ⁹Be H, or C ₁-C ₁₀Alkyl;

R ¹⁰Be H, C ₁-C ₁₀Alkyl, carbocylic radical, assorted carbocylic radical, C ₁-C ₁₀Alkyl-C (=O)-, carbocylic radical-C (=O)-, assorted carbocylic radical-C (=O)-, carbocylic radical alkyl-C (=O)-, assorted carbocylic radical alkyl-C (=O)-, C ₁-C ₁₀Alkyl-S (=O) ₂-, carbocylic radical-S (=O) ₂-, assorted carbocylic radical-S (=O) ₂-, carbocylic radical alkyl-S (=O) ₂-, assorted carbocylic radical alkyl-S (=O) ₂-, C ₁-C ₁₀Alkyl-NHC (=O)-, carbocylic radical-NHC (=O)-, assorted carbocylic radical-NHC (=O)-carbocylic radical alkyl-NHC (=O)-, assorted carbocylic radical alkyl-NHC (=O)-, C ₁-C ₁₀Alkyl-OC (=O)-, carbocylic radical-OC (=O)-, assorted carbocylic radical-OC (=O)-, carbocylic radical alkyl-OC (=O)-, assorted carbocylic radical alkyl-OC (=O)-, or amino protecting group; R wherein ¹⁰The optional replacement with 1,2 or 3R ²³

Q is-B (OH) ₂,-B (OR ¹⁴) ₂, or the ring-type boric acid ester, wherein said boric acid ester contains 2-20 carbon atom, and optional heteroatoms N, S, or O;

R ^ABe C ₁-C ₂₀Alkyl, the optional replacement with R ²⁰

C ₂-C ₂₀Thiazolinyl, the optional replacement with R ²⁰

C ₂-C ₂₀Alkynyl, the optional replacement with R ²⁰

Carbocylic radical, the optional replacement with 1-5R ²¹Or

Assorted carbocylic radical, the optional replacement with 1-5R ²¹

R ²⁰Be selected from:

R ^20bIt is amino protecting group;

R ^20cBe carbocylic radical, the optional replacement with 1-5R ²²Or

Assorted carbocylic radical, the optional replacement with 1-5R ²²

R ²¹Be selected from:

R ²²Be selected from:

R ²³Be selected from:

C ₁-C ₆Alkyl, C ₂-C ₆Thiazolinyl, C ₂-C ₆Alkynyl, F, Cl, Br, I, haloalkyl ,-NH ₂,-NHR ^23a,-N (R ^23a) ₂,-N ₃,-NO ₂,-CN ,-CNO ,-CNS ,-C (=O) OR ^23a,-C (=O) R ^23a,-OC (=O) R ^23a,-N (R ^23a) C (=O) R ^23a,-C (=O) N (R ^23a) ₂, urea groups ,-OR ^23a,-SR ^23a,-S (=O) ₂-(C ₁-C ₆Alkyl) ,-S (=O) ₂-(C ₁-C ₆Alkyl) ,-S (=O) ₂-aryl and-S (=O) ₂-N (R ^23a) ₂

R ^23aBe H or C ₁-C ₆Alkyl;

R is 2,3,4, or 5.

R ²Be H;

R ^ABe C ₁-C ₂₀Alkyl, the optional replacement with R ²⁰

C ₂-C ₂₀Thiazolinyl, the optional replacement with R ²⁰

C ₂-C ₂₀Alkynyl, the optional replacement with R ²⁰

Carbocylic radical, the optional replacement with 1-5R ²²Or

Assorted carbocylic radical, the optional replacement with 1-5R ²²

R ²⁰Be selected from:

-OR ^20a,-SR ^20a,-S (=O) R ^20a,-S (=O) ₂R ^20a,-S (=O) ₂-NHR ^20a,-SC (=O) R ^20a,-C (=O) R ^20a,-C (=O) NHR ^20a,-C (=O) O-R ^20a, phthalimido ,-(O-alkyl) _r,-O-alkyl-OH ,-(O-alkyl) _r-OH ,-OR ^20c,-SR ^20c,-O-alkyl-R ^20c,-S-alkyl-R ^20c,-S (=O)-R ^20c,-S (=O) ₂-R ^20c,-S (=O) ₂-NHR ^20c,-SC (=O) R ^20c,-C (=O) R ^20c,-C (=O) OR ^20c,-C (=O) NHR ^20c, the optional replacement with 1-5R ²²Carbocylic radical; Replace with 1-5R with optional ²²Assorted carbocylic radical;

R ^20cBe carbocylic radical, the optional replacement with 1-5R ²²Or

Assorted carbocylic radical, the optional replacement with 1-5R ²²

R ²²Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, phenyl, halogen, haloalkyl, alkoxyl group; Thio alkoxy, amino, alkylamino, dialkyl amido, carboxyl; Alkyl-OC (=O)-, alkyl-C (=O)-, aryl-OC (=O)-, alkyl-OC (=O) NH-; Aryl-OC (=O) NH-, alkyl-C (=O) NH-, alkyl-C (=O) O-, (alkyl-O) _r-alkyl, and HO-(alkyl-O) _r-alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, alkyl-S (=O)-, alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-; With

R is 2,3,4,5,6,7,8,9, or 10.

In further embodiment:

X is R ^AC (=O)-, R ^ANHC (=O)-, R ^AS (=O) ₂-, or R ^A

R ^ABe optional with R ²⁰Substituted C ₁-C ₁₄Alkyl; R ²⁰Be-(O-alkyl) _r-OH, or-(O-alkyl) _r-(O-alkyl); With r be 1,2,3,4, or 5.In further embodiment, said O-alkyl is a methoxyl group, oxyethyl group, or propoxy-.

In further embodiment, the present invention provides the compound of formula (I), or its pharmacologically acceptable salt, steric isomer or tautomer form, wherein:

R ¹It is the 2-propyl group;

R ²Be-CH ₂CH ₂CH ₂NHC (=NH) NH-NO ₂,-CH ₂CH ₂CH ₂NHC (=O) NH ₂,-CH (CH ₃) OH ,-CH ₂CONH ₂,-CH ₂NH ₂, or-CH ₂NR ⁹R ¹⁰

R ⁹Be H;

R ¹⁰Be methyl-C (=O)-, ethyl-C (=O)-, propyl group-C (=O)-, butyl-C (=O)-, amyl group-C (=O)-, 2-(ethoxy carbonyl) ethyl-C (=O)-, 4-methyl-phenyl-C (=O)-, cyclopropyl-C (=O)-, 4-fluoro-phenyl-C (=O)-, 4-H ₂NSO ₂-phenyl-C (=O)-, 4-H ₃CSO ₂-phenyl-C (=O)-, 4-phenyl-phenyl-C (=O)-, 3,4-dimethoxy-benzyl-C (=O)-; 3-pyridyl-C (=O)-, 2-(hydroxyl)-pyridin-3-yl-C (=O)-, 6-(morpholinyl)-pyridin-3-yl-C (=O)-, 2-(pyridin-4-yl) thiazole-4-base-C (=O)-; 2-pyrazinyl-C (=O)-, 2,5-dimethyl--pyrazolyl-C (=O)-; N-methyl-2-pyrryl-C (=O)-, 2-pyrrolidyl-C (=O)-, 2-thiophenyl-C (=O)-; 5-isoxazolyl-C (=O)-, 4-(tetrazolium-5-yl) phenyl-C (=O)-, (5-tetrazyl) CH ₂-C (=O)-, N-H ₃CSO ₂-piperidyl-C (=O)-, butyl-OC (=O)-, (benzyl)-OC (=O)-, (9-fluorenyl methyl)-OC (=O)-, amyl group-NHC (=O)-, propyl group-NHC (=O)-, phenyl-NHC (=O)-, 4-methyl-phenyl-NHC (=O)-, methyl-S (=O) ₂-, 4-fluoro-phenyl-S (=O) ₂-, 4-cyanic acid-phenyl-S (=O) ₂-, 1-methyl-imidazol-4 yl-S (=O) ₂-, 2-thiophenyl-S (=O) ₂-, (4-methyl-phenyl)-NHC (=O) NH-S (=O) ₂-and (4-methyl-phenyl)-S (=O) ₂NHC (=O)-,

Perhaps, R ⁹And R ¹⁰The N atom that connects with them forms pyrryl or pyrazolyl;

X is R ^AC (=O)-, R ^ANHC (=O)-, R ^AS (=O) ₂-, or R ^AOC (=O)-;

R ^ABe CH ₃-, C ₂H ₅-, C ₃H ₇-; C ₄H ₉-, C ₅H ₁₁-, C ₆H ₁₃-, C ₇H ₁₅-, C ₈H ₁₇-, C ₉H ₁₉-, C ₁₀H ₂₁-, C ₁₁H ₂₃-, C ₁₂H ₂₅-, C ₁₃H ₂₇-, adamantyl-, the bicycloheptane base-, with R ²⁰Substituted C _1-3Alkyl; With R ²⁰Substituted C _2-10Thiazolinyl; With 0-3R ²¹Substituted cyclopropyl; With 0-2R ²¹Substituted cyclopentyl; With 0-2R ²¹Substituted cyclohexyl; With 0-3R ²¹Substituted phenyl; With 0-2 R ²¹Substituted naphthyl; With 0-1 R ²¹Substituted pyrazinyl; With 0-1R ²¹Substituted quinolyl; With 0-1 R ²¹Substituted imidazolyl; With 0-1 R ²¹Substituted tetrahydrofuran base; With 0-1 R ²¹Substituted oxo thiazolidyl; With 0-1 R ²¹Substituted benzothiazolyl; With 0-2 R ²¹Substituted thiazolyl; With 0-2 R ²¹Substituted furyl; With 0-1 R ²¹Substituted pyrrolidyl; With 0-1 R ²¹Substituted piperidyl; With 0-1 R ²¹Substituted piperazinyl; Or with 0-1 R ²¹Substituted pyridyl;

R ²⁰Be selected from:

Hydroxyl-, methoxyl group-, oxyethyl group-, propoxy--, butoxy-, pentyloxy-; Hexyl oxygen base-, heptyl oxygen base-, octyl group oxygen base-, methoxy ethoxy-, the methoxy ethoxy oxyethyl group-, methyl-S-; Ethyl-S-, octyl group-S-, methyl-C (=O) S-, (kharophen) methyl-S-, amino-; Methylamino-, dimethylamino-, methyl-C (=O)-, phenyl-C (=O)-, (H ₃CSO ₂) phenyl-C (=O)-, thiophenyl-C (=O)-, methyl-OC (=O)-, ethyl-OC (=O)-, butyl-OC (=O) NH-, methyl-C (=O) NH-, methoxy ethoxy-methyl-C (=O) NH-, H ₂NC (=O)-, methyl-NHC (=O)-, ethyl-NHC (=O)-, propyl group-NHC (=O)-, phenyl-NHC (=O)-, H ₂NC (=O) NH-, H ₂NS (=O) ₂-, octyl group-S (=O) ₂-, phenyl-S (=O) ₂-, aminomethyl phenyl-S (=O) ₂-, thiophenyl-S (=O) ₂-, cyclopentyl-, cyclohexyl-, suberyl-, adamantyl-, the bicycloheptane base-, cyclopentenyl-; Phenyl-, methoxyl group-phenyl-, methyl-phenyl-, dimethyl--phenyl-, ethyl-phenyl-, propyl group-phenyl-, butyl-phenyl-; The fluoro-phenyl-, two fluoro-phenyl-, the chloro-phenyl-, the bromo-phenyl-, the iodo-phenyl-, dimethylamino-phenyl-, cyclohexyl oxygen base-; 2-sec.-propyl-5-methyl-cyclohexyl base oxygen base-, naphthyl-, the methoxyl group naphthyl-, naphthyl oxygen base-, phenoxy-, (methyl-phenyl) oxygen base-, (ethyl-phenyl) oxygen base-; (propyl group-phenyl) oxygen base-, (butyl-phenyl) oxygen base-, (fluoro-phenyl) oxygen base-, (chloro-phenyl) oxygen base-, (bromo-phenyl) oxygen base-, naphthyl-S-, benzyl-S-; (methyl-phenyl) methyl-S-, pyrimidyl-S-, piperidyl-, N-methyl-piperidyl-, N-propyl group-piperidyl-, phthalimido-, thiophenyl-; Methyl-thiophenyl-, imidazolyl-, furnayl-, tetrazyl-, the oxo-pyrrolidine base-, indyl-, and methyl-indyl-; With

R ²¹Be selected from:

Methyl-, ethyl-, propyl group-, butyl-, amyl group-, hexyl-, heptyl-; Vinyl-, propenyl-, crotonyl-, methoxyl group-, oxyethyl group-, propoxy--, phenoxy-; Fluoro-, chloro-, bromo-, methyl-C (=O)-, butyl-OC (=O)-, butyl-OC (=O) NH-, phenyl-; P-methoxy-phenyl-, fluorophenyl-, chloro-phenyl--, bromophenyl-, pyrryl-, and pyridyl-.

Should be appreciated that for the sake of clarity in the embodiment of separating, describe some characteristic of the present invention, these characteristics also can be combined in the single embodiment and provide.On the contrary, also can separately provide or provide for the of the present invention multiple different characteristics of in single embodiment, describing for purpose of brevity with any suitable inferior array configuration.

" boric acid " used herein refers to contain B (OH) ₂The compound of part.In some embodiments, boronic acid compounds can form the oligomerization acid anhydride through the dehydration of boric acid part.For example, Snyder etc., J.Am.Chem.Soc., 1958,80,3611 report oligomerization aryl boric acids.Therefore, except as otherwise noted, " boric acid ", or contain B (OH) ₂The chemical general formula of part is intended to comprise free boric acid, and the oligomerization acid anhydride includes but not limited to dimer, tripolymer, tetramer and composition thereof.

Used herein, " boron trioxide " or " boric anhydride " refers to the boronic acid compounds molecular combinations with two or more general formulas (I), partly loses one or more water moleculess and the compound that forms from boric acid.When contact with water, the boron trioxide compound can be discharged free boronic acid compounds by aquation.In some embodiments, the boron trioxide structure can comprise two, and three, four or more boric acid unit also can have ring-type or linear configuration.In some embodiments, the boron trioxide compound exists with single oligomer form basically; Yet boron trioxide also comprises the different oligomerization boron trioxides and the mixture of free boric acid.

The nonrestrictive example of boron trioxide of the present invention comprises general formula (II) and compound (III), and wherein G is the part of general formula (IV), and t is 0 to 10 or 1,2,3, or 4.

In some embodiments, about at least 80% boric acid exists with single oligomerization acid anhydride form in the boron trioxide compound.In other embodiment, about at least 85 in the boron trioxide compound, about 90, about 95, or about 99% boric acid exists with single oligomerization acid anhydride form.In some embodiments, the boron trioxide compound is made up of single oligomerization boron trioxide basically.In other embodiment, the boron trioxide compound is made up of single oligomerization boron trioxide.In other embodiment, the boron trioxide compound comprises the boroxin (boroxine) of general formula (III), and wherein t is 1.

The boron trioxide compound can for example comprise through being exposed to dehydration conditions, crystallization, and freeze-drying is exposed to heat and/or is exposed to siccative and prepares self-corresponding boronic acid compounds.Some suitable recrystallisation solvents comprise ETHYLE ACETATE, methylene dichloride, hexane, ether, benzene, acetonitrile, ethanol and composition thereof.

Used herein, " boron ester " or " boric acid ester " refer to the ester derivative of boronic acid compounds.Used herein; " ring-type boric acid ester " is used to represent general formula-B (OR) stable ring-type boric acid part (OR); Wherein two R substituting groups are joined together to form loop section (for example 3 to 10 Yuans naphthenic base), optional further replace with one or more substituting groups or condense with (sharing at least one key) one or more other carbocylic radicals or assorted carbocylic radical.Ring-type boron ester can contain 2 to 20 carbon atoms, and optional contains N, S, or the heteroatoms of O.The ring-type boric acid ester is well known in the art.The example of ring-type boric acid ester includes but not limited to, pinine glycol boric acid ester, which pure boric acid ester quite, 1 boric acid ester, 1, ammediol boric acid ester; 1,2-Ucar 35 boric acid ester, 2,3-butyleneglycol boric acid ester, 1,1,2; 2-tetramethylethylene glycol boric acid ester, 1,2-di-isopropyl glycol borate, 5,6-decanediol boric acid ester, 1,2-dicyclohexyl glycol borate; Dicyclohexyl-1,1 '-glycol, diethylolamine boric acid ester and 1,2-xenyl-1 boric acid ester.

Ring-type boric acid ester in some embodiments, " " have a formula (II-a):

Wherein:

D is a disappearance, O, S, NR ¹⁶, or CR ^15eR ^15f

R ^15a, R ^15b, R ^15c, R ^15d, R ^15e, R ^15fBe H independently of one another, C ₁-C ₁₀Alkyl, C ₃-C ₇Naphthenic base, aryl or heteroaryl, wherein said C ₁-C ₁₀Alkyl, C ₃-C ₁₀Naphthenic base, aryl or heteroaryl are optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces;

Perhaps, R ^15aAnd R ^15bThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base or 3-to 10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces;

Perhaps, R ^15cAnd R ^15dThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base or 3-to 10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces;

Perhaps, R ^15bAnd R ^15cThe C atom that connects with them forms aryl, heteroaryl, C with insertion D part ₃-C ₁₀Naphthenic base or 3-to 10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces;

R ¹⁶Be H or C ₁-C ₆Alkyl; With

P and q are respectively 1,2 or 3 independently.

In some embodiments, D lacks.

In some embodiments, D is NR ¹⁶

In some embodiments, D is NH.

In some embodiments, D is CH ₂

In some embodiments, R ^15aAnd R ^15bThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base or 3-to 10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces; And R ^15cAnd R ^15dThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base or 3-to 10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces.

In some embodiments, R ^15aAnd R ^15bThe C atom that connects with them forms cyclopropyl, cyclobutyl, cyclopentyl (cyclopenytyl), cyclohexyl or suberyl; And R ^15cAnd R ^15dThe C atom that connects with them forms cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl or suberyl.

In some embodiments, D lacks, and R ^15bAnd R ^15cThe C atom that connects with them forms aryl, heteroaryl, C ₃-C ₁₀Naphthenic base or 3-to 10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogen ropes, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces.

In some embodiments, D lacks, and R ^15bAnd R ^15cThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base, optional by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, alkylamino, dialkyl amido, aryl, or heteroaryl replaces.

In some embodiments, D lacks, and R ^15bAnd R ^15cThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base, optional by 1,2,3 or 4 halogens or C ₁-C ₄Alkyl replaces.

In some embodiments, D lacks, and R ^15bAnd R ^15cThe C atom that connects with them forms C ₇-C ₁₀The bicyclic ring alkyl, optional by 1,2,3 or 4 halogens or C ₁-C ₄Alkyl replaces.

In some embodiments, p and q each naturally 1.

In some embodiments, R ^15a, R ^15b, R ^15c, R ^15dIn at least one is not H.

Other examples as at " the ring-type boric acid ester " of this definition comprise the boric acid ester with structure:

and

Wherein: W replaces or unsubstituted C ₄-C ₁₀Cycloalkyl ring or replacement or unsubstituted benzyl ring; W ¹Be to replace or unsubstituted C independently when occurring at every turn ₃-C ₆Cycloalkyl ring.Radicals R ^15a, R ^15b, R ^15c, R ^15d, R ^15e, R ^15f, p and q as above define.

Used herein, term " alkyl " or " alkylidene group " are used to represent the saturated hydrocarbyl of straight or branched.The example of alkyl comprises methyl (Me), ethyl (Et), propyl group (as, n-propyl group and sec.-propyl), butyl (as, n-butyl, isobutyl-, s-butyl, t-butyl), amyl group (as, n-amyl group, isopentyl, neo-pentyl) etc.Alkyl can comprise from 1 to about 20, from 2 to about 20, from 1 to about 10, from 1 to about 8, from 1 to about 6, from 1 to about 4, or from 1 to about 3 carbon atoms.

Used herein, " thiazolinyl " refers to have the alkyl of one or more carbon-carbon double bonds.The example of thiazolinyl comprises vinyl, propenyl, crotonyl, pentenyl, hexenyl, butadienyl, piperylene base, dialkylene etc. between oneself.

Used herein, " alkynyl " refers to have one or more carbon carbon triple-linked alkyl.The example of alkynyl comprises ethynyl, proyl, butynyl, pentynyl etc.

Used herein, " alkylhalide group " refers to have the alkyl of one or more halogenic substituents.The example of alkylhalide group comprises CF ₃, C ₂F ₅, CHF ₂, CCl ₃, CHCl ₂, C ₂Cl ₅Deng.All Wasserstoffatomss can be called " perhaloalkyl radical " by the substituted alkyl of halogen atom.The example of perhaloalkyl radical comprises CF ₃And C ₂F ₅

Used herein, " carbocylic radical " is the cyclic hydrocarbon part of saturated (promptly not containing two keys or triple bond) or undersaturated (that is, containing one or more pairs of keys or triple bond).Carbocylic radical can be monocycle or polycyclic.The example of carbocylic radical comprises cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, suberyl; Cyclopentenyl, 1,3-ring piperylene base, cyclohexenyl, norcamphyl (norbornyl); Pinane base (norpinyl) falls, norcaryl (norcarnyl), adamantyl (adamantyl), phenyl etc.Carbocylic radical can be aromatics (as, " aryl ") or non-aromatics (as, " naphthenic base ").In some embodiments, carbocylic radical can have from 3 to about 20,3 to about 10, or 3 to about 7 carbon atoms.

Used herein, " aryl " refers to aromatic carbocyclyl groups, comprises for example phenyl of monocycle or polycyclic aromatic hydrocarbons, naphthyl, anthryl, phenanthryl, indanyl, indenyl etc.In some embodiments, aryl has from 6 to about 18 one-tenth ring carbon atoms.

Used herein, " naphthenic base " refers to non-aromatic carbocyclyl groups, comprises the alkyl of cyclisation, thiazolinyl, and alkynyl.Naphthenic base can comprise two ring or multi-loop systems.The example of naphthenic base comprises cyclopropyl, cyclobutyl, and cyclopentyl, cyclohexyl, suberyl, cyclopentenyl, cyclohexenyl, the cyclohexadiene base, the cycloheptatriene base, the pinane base falls in norcamphyl, norcaryl, adamantyl etc.The definition of naphthenic base also comprises the part that has with cycloalkyl ring the one or more aromatic rings that condense (promptly shared with it key), for example, and the benzo derivative of pentamethylene (indanyl), the benzo derivative of hexanaphthene (tetralyl) etc.In some embodiments, naphthenic base has 3,4,5,6, or 7 become ring carbon atom.In some embodiments, naphthenic base has 0,1, or 2 two or three one-tenth ring keies.

Used herein, " assorted carbocylic radical " can be saturated or unsaturated carbocylic radical, and wherein one or more one-tenth ring carbon atoms of carbocylic radical are by heteroatoms O for example, S, or N replaces.Assorted carbocylic radical can be aromatics (as, " heteroaryl ") or (like " Heterocyclylalkyl ") of non-aromatics.Assorted carbocylic radical is corresponding to hydrogenation or partially hydrogenated heteroaryl.Assorted carbocylic radical can comprise from about 1 to about 20, about 2 to about 10 except at least one heteroatoms, or about 2 arrive about 7 carbon atoms, and can connect through carbon atom or heteroatoms.The example of assorted carbocylic radical comprises morpholinyl, thio-morpholinyl, piperazinyl, tetrahydrofuran base, tetrahydro-thienyl; 2,3-dihydro benzo furyl, 1,3-benzo dioxole (benzodioxole), phendioxin; The 4-diox, piperidyl, pyrrolidyl, isoxazole alkyl, isothiazole alkyl; Pyrazolidyl ， oxazolidinyl, thiazolidyl, imidazolidyl etc.

Used herein, " heteroaryl " is the assorted carbocylic radical of aromatics and comprises having for example sulphur of at least one heteroatomic ring member, the monocycle of oxygen or nitrogen and polycyclic aromatic hydrocarbons.Heteroaryl includes, without being limited to, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl, furyl, quinolyl; Isoquinolyl, thienyl, imidazolyl, thiazolyl, indyl, pyrryl ， oxazolyl, benzofuryl; Benzothienyl, benzothiazolyl ， isoxazolyl, pyrazolyl, triazolyl, tetrazyl indazolyl, 1; 2,4-thiadiazolyl group, isothiazolyl, benzothienyl, purine radicals, carbazyl, benzimidazolyl-etc.In some embodiments, heteroaryl can have from 3 to about 20 and becomes ring carbon atoms, and heteroaryl has from about 3 to about 12 and becomes ring carbon atoms in other embodiment.In some embodiments, heteroaryl has 1 to about 4,1 to about 3, or 1 to 2 heteroatoms.

Used herein, " Heterocyclylalkyl " refers to the non-aromatics carbocylic radical of mixing, and comprises the alkyl of cyclisation, thiazolinyl, and alkynyl, and wherein one or more become ring carbon atoms by heteroatoms O for example, N, or the S atom replaces.Become ring carbon and heteroatoms, such as S and N, can be further oxidized in the Heterocyclylalkyl part.For example, become ring carbon or heteroatoms carry one or two oxygen or sufido part (for example,＞C=O,＞S=O,＞S (=O) ₂, N → O etc.).Also be included in the definition of Heterocyclylalkyl is to have the part that one or more and non-aromatic heterocyclic condense the aromatic ring of (promptly shared with it key); Phthalimide-based for example; Naphthalimido pyromellitic diimide base; The benzo derivative of phthalanyl and saturated heterocyclic is indoles thiazolinyl (indolene) and isoindole thiazolinyl for example.In some embodiments, Heterocyclylalkyl has 3 to about 20 one-tenth annular atomses.In some embodiments, Heterocyclylalkyl has 3,4,5,6, or 7 become annular atoms.In some embodiments, Heterocyclylalkyl has 0,1, or 2 two or three one-tenth ring keies.

Used herein, " halogen " or " halogen " comprises fluorine, chlorine, bromine and iodine.

Used herein, " alkoxyl group " refers to-the O-alkyl group.The example of alkoxyl group comprises methoxyl group, oxyethyl group, propoxy-(as, n-propoxy-and isopropoxy), t-butoxy etc.In some embodiments, alkoxyl group has 1-20,1-12,1-8,1-6,1-4, or 1-3 carbon atom.

Used herein, " alkoxyl group alkoxyl group " refers to-O-alkyl-O-alkyl.

Used herein, " thio alkoxy " refers to that wherein the O atom is by the substituted alkoxyl group of S atom.

Used herein, " aryloxy " refers to-the O-aryl.Examples of aryloxy is a phenoxy.

Used herein, " thio-aryloxy " refers to that wherein the O atom is by the substituted aryloxy of S atom.

Used herein, " aralkyl " refers to by the substituted moieties of aryl.The example of aralkyl comprises benzyl and menaphthyl.In some embodiments, aralkyl has from 7 to 11 carbon atoms.

Used herein, " amino " refers to NH ₂" alkylamino " refers to by the substituted amino of alkyl, and " dialkyl amido " refers to by two substituted amino of alkyl.On the contrary, " aminoalkyl group " refers to by the substituted alkyl of amino.

Used herein, " carbonyl " refers to＞C=O.

Used herein, " carboxyl " refers to-COOH.

Used herein, " hydroxyl " refers to-OH.

Used herein, " sulfydryl " refers to-SH.

Used herein, " urea groups " refers to-NHCONH ₂

Used herein, " sulfinyl " refers to＞SO.

Used herein, " sulphonyl " refers to＞SO ₂

Used herein, " oxygen base " refers to-O-.

The combination of the above-mentioned technical term of chemistry is meant the part of the combination that contains chemical group.This combination term is understood as that the substituting group of following term usually.For example, " alkyl-carbonyl thiazolinyl " refers to by the thiazolinyl of carbonyl substituted, and carbonyl is replaced by alkyl.Following term also can illustrate this combination.

Used herein, " carbocylic radical alkyl " refers to by the substituted moieties of carbocylic radical.The example of carbocylic radical alkyl comprises " aralkyl " (by the substituted alkyl of aryl) and " cycloalkylalkyl " (by alkyl of cycloalkyl substituted).

Used herein, " carbocylic radical thiazolinyl " refers to by the substituted alkenyl part of carbocylic radical.The example of carbocylic radical thiazolinyl comprises " arylalkenyl " (by the substituted thiazolinyl of aryl) and " naphthenic base thiazolinyl " (by thiazolinyl of cycloalkyl substituted).

Used herein, " carbocylic radical alkynyl " refers to by the substituted alkynyl part of carbocylic radical.The example of carbocylic radical alkynyl comprises " sweet-smelling alkynyl " (by the substituted alkynyl of aryl) and " naphthenic base alkynyl " (by alkynyl of cycloalkyl substituted).

Used herein, " assorted carbocylic radical alkyl " refers to by the substituted moieties of assorted carbocylic radical.The example of assorted carbocylic radical alkyl comprises " heteroarylalkyl " (by the substituted alkyl of heteroaryl) and " Heterocyclylalkyl alkyl " (by the substituted alkyl of Heterocyclylalkyl).

Used herein, " assorted carbocylic radical thiazolinyl " refers to by the substituted alkenyl part of assorted carbocylic radical.The example of assorted carbocylic radical thiazolinyl comprises " heteroaryl thiazolinyl " (by the substituted thiazolinyl of heteroaryl) and " Heterocyclylalkyl thiazolinyl " (by the substituted thiazolinyl of Heterocyclylalkyl).

Used herein, " assorted carbocylic radical alkynyl " refers to by the substituted alkynyl part of assorted carbocylic radical.The example of assorted carbocylic radical alkynyl comprises " heteroaryl alkynyl " (by the substituted alkynyl of heteroaryl) and " heterocycle alkynyl alkyl " (by the substituted alkynyl of Heterocyclylalkyl).

Used herein, " protection base " refers to and can selectivity be connected to for example hydroxyl of functional group, amino and carboxyl and from its chemical functional group who removes.It is inert functional group that protection base is introduced in the chemical cpd to produce the chemical reaction condition that this compound was exposed usually.In the kinds of protect base any one can be used for the present invention.The protection base of amino part is called " amino protecting group ", and the protection base of guanidine radicals part is called " guanidine radicals protection base ".Amino and guanidine radicals protection base can have general formula aryl-SO ₂-, alkyl-SO ₂-, aryl-C (=O)-, aralkyl-C (=O)-, alkyl-C (=O)-; Aryl-OC (=O)-, aralkyl-OC (=O)-, alkyl-OC (=O)-, aryl-NHC (=O)-; Alkyl-NHC (=O)-etc., wherein said alkyl, aryl and aralkyl can be substituted or not replace.Example amino and guanidine radicals protection base also can comprise t-butyl oxygen carbonyl (BOC), fluorenyl methoxy carbonyl (Fmoc), benzyloxycarbonyl (Cbz), and phthalimido.Other protection base comprises like the lower section:

Other representational protection bases can be at T.W.Green and P.G.M.Wuts, the protection base in the organic synthesis (Protective Groups in Organic Synthesis), the 3rd edition; Wiley& Sons; Inc., New York (1999) finds, and it draws in full at this and is reference.

Used herein, at least one Wasserstoffatoms in " substituted " expression chemical group is replaced by non-hydrogen partial.Substituent example comprises F, Cl, Br, I, C ₁-C ₆Alkyl, C ₁-C ₆Thiazolinyl, C ₁-C ₆Alkynyl, alkylhalide group, NR ^ER ^F, N ₃, NO ₂, CN, CNO, CNS, C (=O) OR ^E, R ^ECO, R ^EC (=O) O, R ^ECONR ^E, R ^ER ^FNCO, urea groups, OR ^E, SR ^E, SO ₂-alkyl, SO ₂-aryl, and SO ₂-NR ^ER ^F, R wherein ^EAnd R ^FIndependently be respectively H or C ₁-C ₆Alkyl.Perhaps, R ^EAnd R ^FCan be combined to form 5 to 7 element heterocycles with the nitrogen that is connected on it, for example pyrrolidyl, piperidyl, morpholinyl, piperazinyl and N methyl piperazine base.When the chemical group when here was " substituted ", it can have and reaches whole valencys and replace, as long as the compound that obtains is stable compound or stable structure; For example, methyl can be by 1,2, or 3 substituting groups replace, and methylene radical can be replaced by 1 or 2 substituting group, and phenyl can be by 1,2,3,4, or 5 substituting group replacements etc.

" leavings group " used herein refers to after nucleophilic substitution by the displaced any group of nucleophilic reagent.The example of leavings group comprise halogen (F, Cl, Br, I), hydroxyl; Alkoxyl group, sulfydryl, thio alkoxy, triflate, alkyl sulphonyl; Substituted alkyl sulfonic ester, aromatic yl sulphonate, substituted aromatic yl sulphonate, heterocycle sulphonate or tribromo-acetyl imido-ester (trichloroacetimidate).Representative example comprises p-(2,4-dinitrobenzene amido) benzene sulfonate, benzene sulfonate, methanesulfonate ester, p-toluene sulfonic acide ester; P-bromo-benzene sulfonic acid ester, tribromo-acetyl imido-ester, acyloxy, 2,2; 2-trifluoro esilate, imidazoles alkylsulfonyl and 2,4,6-trichlorophenyl.

" stable compound " used herein or " stable structure " refer to enough stablize to experience the purity that from reaction mixture, is separated to useful degree, and preferably can be mixed with the compound of beneficial agents.The present invention only relates to stable compound.

Compound described herein can be asymmetrical (as, have one or more stereocenters).All steric isomers, except as otherwise noted, for example enantiomer and diastereomer are expected.The compound of the present invention that comprises asymmetric substituted carbon atom can separate with optical activity or racemic form.The method that how prepares the optical activity form from the optical activity parent material is well known in the art, and is for example synthetic through resolving racemic mixtures or stereoselectivity.Alkene, many geometrical isomers of the two keys of C=N etc. also can be present in the compound described herein, and all stable like this isomer are all expected by the present invention.The cis of The compounds of this invention and trans geometrical isomer are described and can be separated into mixture of isomers or isolating isomeric forms.

Except that above-mentioned form, compound described herein also can have asymmetric center, causes an enantiomorph of formula (I) compound to show higher BA than corresponding enantiomorph.Two configurations all are regarded as part of the present invention.For example, the R2 substituting group of formula (I) compound or exist with S or with the R configuration.The example of the preferred enantiomorph configuration of the present invention is formula (I-s) compound:

But be not limited to this example.If desired, adopt method well known in the art can realize separation to the racemize material.

Compound of the present invention also comprises tautomeric form, for example the keto-enol tautomerism body.Tautomeric form can be in balance or solid is locked in a kind of form through suitable replacement.

Compound of the present invention also comprises all isotropic substances of atom in intermediate compound or the final compound.Isotropic substance comprises having the same atoms ordinal number but those different atoms of total mass number.For example the isotropic substance of hydrogen comprises tritium and deuterium.

" pharmaceutically useful " is used in reference to compound here; Material; Compsn and/or dosage form, it is suitable for contacting with human and animal's tissue in the scope of reliable medical judgment and does not have overdosage toxicity, stimulates; Anaphylaxis or other problems and complication match with suitable advantage/risk ratio.

The present invention also comprises the pharmaceutically useful salt of compound described herein." pharmaceutically useful salt " used herein refers to the verivate of disclosed compound, and wherein parent compound is modified as its salt form through transforming existing acid or alkali part.The example of pharmaceutically useful salt includes but not limited to that alkaline residue is the inorganic or organic acid salt of amine for example; Acidic residues is alkali or the organic salt etc. of carboxylic acid for example.The pharmaceutically useful salt of the present invention for example comprises the conventional non-toxic salt or the quaternary ammonium salt of the parent compound that forms from nontoxic inorganic or organic acid.For example, so conventional non-toxic salt comprises from mineral acid hydrochloric acid for example, Hydrogen bromide, sulfuric acid, thionamic acid, phosphoric acid, deutero-salt such as nitric acid; With from organic acid acetate for example, propionic acid, Succinic Acid, oxyacetic acid, Triple Pressed Stearic Acid, lactic acid, oxysuccinic acid; Tartrate, Hydrocerol A, xitix, pamoic acid (pamoic), toxilic acid, hydroxymaleic acid; Toluylic acid, L-glutamic acid, phenylformic acid, Whitfield's ointment, Sulphanilic Acid, 2-acetoxy-benzoic acid; Fumaric acid, toluenesulphonic acids, methylsulfonic acid, ethionic acid, oxalic acid, the salt of preparation such as isethionic acid.The pharmaceutically useful salt of the present invention can be synthetic through conventional chemical process from the parent compound that contains alkalescence or acidic moiety.Usually, such salt can be through appropriate base or sour water or the organic solvent with the free acid of these compounds or alkali form and stoichiometry, or the two mixture reaction and preparing.Usually, non-aqueous media such as ether, ETHYLE ACETATE, ethanol, Virahol or acetonitrile are preferred.The list of suitable salt can be at the Remington pharmaceutical science, and the 17th edition, Mack publishing company, Easton, Pa., 1985, p.1418 with at Journal ofPhamaceutical science, find in 66,2 (1977), its disclosed content is drawn at this and is reference.

Synthetic

Compound of the present invention comprises its salt and solvolyte, can use known organic synthesis technology preparation and synthetic according to numerous possible arbitrary route of synthesis.

The reaction for preparing compound of the present invention can be carried out in suitable solvent, and said solvent can easily be selected by the technician in organic synthesis field.The temperature that suitable solvent carries out in reaction, promptly in the scope from the solvent freezing point temperature to the solvent boiling point temperature basically not with parent material (reactant), midbody, or product reaction.Given reaction can be carried out in the mixture of a kind of solvent or more than one solvents.According to concrete reactions step, can select the suitable solvent of concrete reactions step.

The preparation of compound of the present invention comprises the protection of multiple different chemical group and goes protection.Protection and de-protected demand and select suitable protection base easily to determine by those skilled in the art.The chemical property of protection base can, for example, T.W.Green and P.G.M.Wuts, the protection base in the organic synthesis, the 3rd edition, Wiley & Sons, Inc., NewYork finds in (1999), it draws in full at this and is reference.

Can monitor reaction according to any suitable method well known in the art.For example, form through spectrography monitoring product, (for example, such as NMR spectrum ¹H or ¹³C) infrared spectrum, spectrophotometry (for example, UV-is visible), or mass spectrum, or through chromatogram, such as performance liquid chromatography (HPLC) or thin-layer chromatography.

The preparation method of The compounds of this invention can be referring to the described preparation aminoboronic acid in this area, and the method for ester and related compound, such as U.S. patent No.4, and 537,773 and U.S. patent No.5,614,649, draw for referencial use in full at this with it respectively.In some embodiments, compound of the present invention can prepare through order 3 fragment components of coupling (F1, F2, and F3).

The F1 fragment

Compound of the present invention synthetic comprises the boracic fragment (F1) of the structure shown in (A) that has general formula.

The boric acid ester of F1 for example partly comprises, diol ester, and for example the ring of general formula (A) connects shown in the Sauerstoffatom.

Can use asymmetrical boric acid ester group to control when the preparation F1 as far as the stereochemistry of the α position carbon atom of boron atom in the general formula (A).For example, the pinane diol ester of boric acid is beneficial to the pure segmental preparation of F1 of the pure or basic stereochemistry of stereochemistry.As an example; The segmental preparation method of F1 is following: the compound (showing the pinine glycol boric acid ester available from (+)-pinine glycol) of general formula (B) is reacted in the presence of methylene dichloride or methylene bromide with highly basic (like diisopropylaminoethyl lithium or dicyclohexyl lithium amide); Add Lewis acid subsequently (like, ZnCl ₂, ZnBr ₂, or FeCl ₃) be the compound (wherein L is a halogen) of the general formula (C) of carbon place, α position to be created in stereocenter of new introducing to boron.

Formula (C) compound then with alkaline acid amides (for example; Two (trimethyl silyl) lithium amide; Two (trimethyl silyl) sodium amide; With two (trimethylammonium potassium siloyl group) amination potassium) reaction, or import amido (NR with the new stereocenter that forms of effective conversion (such as through SN2 type mechanism) and in halogen (for example, chlorine) group position ₂) the reaction of other nucleophilic reagents, thereby (wherein R for example is to the formula of formation (D) compound, alkyl, Si (alkyl) ₃, aryl, or aralkyl).

Formula (D) compound can be further with can be with NR ₂Groups converted is NH ₂Reagent or its reactant salt, the F1 fragment of formation can be connected with other fragments through amine basically.With NR ₂Groups converted is NH ₂Suitable agent be the HCl protonic acid, such as as R when being silyl (for example, trimethyl silyl).

The compound of general formula (B) can also prepare according to two-stage process, comprises the tri-alkoxy borine, and preferred three isopropoxy borines are with (1S; 2S, 3R, 5S)-(+) the pinine glycol reaction produces monoalkoxy [(1S, 2S; 3R, 5S)-(+) pinine glycol] the borine midbody, wherein two alkoxyl groups in the tri-alkoxy borine are by (1S; 2S, 3R, 5S)-(+) pinine glycol replaces.Blended pinine glycol alkoxyl group borine, with suitable Organometallic derivatives Grignard reagent R for example ¹CH ₂MgBr or lithium alkylide R ¹CH ₂Li reaction back produces yield and the high compound (B) of purity.In the flow process below the method that produces the compound of midbody blended pinine glycol isopropoxy borine (F) and general formula (B) since three isopropoxy borines is shown in,

And be recited in the embodiment of the invention A.2 in.

Therefore, the invention further relates to the preparation method of formula (II) compound:

Wherein variable composition as above defines, with the glycol of formula (II-b):

Suitable tri-alkoxy borine with formula (II-a):

Each R wherein ¹⁷Be C independently ₁-C ₁₀Alkyl or C ₃-C ₁₀Naphthenic base;

Under the condition of the tri-alkoxy borine midbody that is suitable for forming blended formula (II-c), react for some time:

And make formula (II-c) midbody or and i) formula R ¹CH ₂MX ^HalReagent, wherein M is metal and X ^HalBe halogen atom, or with ii) formula R ¹CH ₂The reagent of Li reacts for some time under the condition that is suitable for the formula that forms (II) compound.

In some embodiments, R ¹⁷Be C ₁-C ₄Alkyl.

In some embodiments, R ¹⁷It is sec.-propyl.

In some embodiments, the glycol of formula (II-b) is a pinine glycol, tetramethyl ethylene ketone, and dicyclohexyl-1,1 '-glycol, 1,1; Ammediol, 1,2-Ucar 35,2,3-butyleneglycol, 1,1; 2,2-tetramethylethylene glycol, 1,2-di-isopropyl terepthaloyl moietie, 5,6-decanediol, 1; 2-dicyclohexyl terepthaloyl moietie, dicyclohexyl-1,1 '-glycol, diethylolamine, or 1,2-xenyl-1.

In some embodiments, the glycol of formula (II-b) is a pinine glycol.

In some embodiments, formula R ¹CH ₂MX ^HalIt is Grignard reagent.

In some embodiments, formula R ¹CH ₂MX ^HalBe R ¹CH ₂MgBr.

In some embodiments, R ¹It is sec.-propyl.

In some embodiments, the present invention provides the preparation method of formula (II-i) compound:

Comprise:

A) will (1S, 2S, 3R, 5S)-(+)-pinine glycol and three isopropoxy borines react for some time under the condition that is suitable for the formula that forms (II-ii) midbody:

And b) formula (II-ii) midbody and isobutyl-magnesium bromide are reacted for some time under the condition that is suitable for the formula that forms (II-i) compound.

In some embodiments, the present invention provides formula (II-ii) compound:

In any suitable solvent, carry out reactions step, said solvent and reagent and product right and wrong are reactive, and allow mix reagent under the temperature (for example, subambient temperature) that reduces.The solvent that is fit to comprises ether, such as Methylal(dimethoxymethane), and THF, 1; The 3-diox, 1,4-diox, furans; Anaesthetie Ether, ethylene glycol dimethyl ether, ethylene glycol bisthioglycolate ethyl ether, diethylene glycol dimethyl ether; Diethylene glycol diethyl ether, triethylene glycol dimethyl ether, phenylmethylether, or t-butyl methyl ether.In some embodiments, ether solvents contains THF and/or Anaesthetie Ether.

Being reflected under the suitable temp in the said method carried out, and said temperature can be confirmed by those skilled in the art easily.Temperature of reaction will depend on, for example, and the melting point and the boiling point of reagent and solvent (if existence); The thermokinetics of reaction (for example, the heating strong reaction must be carried out under the reduction temperature); And the kinetics (for example, overactivity energy barrier need improve temperature) of reaction." temperature of raising " is meant the temperature that is higher than room temperature (greater than 22 ℃), and " temperature of reduction " is meant subambient temperature.

In some embodiments, suitable temperature is the temperature that reduces.The prepared in reaction blended tri-alkoxy borine midbody of tri-alkoxy borine and glycol can, for example about-20 ℃ are carried out to about 10 ℃ temperature.In some embodiments, the reaction of tri-alkoxy borine and glycol can be carried out under about 0 ℃.Blended tri-alkoxy borine midbody and organometallic reagent R ¹CH ₂MX ^HalOr alkyl lithium reagents R ¹CH ₂The reaction of Li can be carried out under for example making an appointment with-100 to-20 ℃.In some embodiments, blended tri-alkoxy borine midbody and R ¹CH ₂MX ^HalBe reflected at approximately-78 ℃ under carry out.

Reaction in the said method can be carried out under air or inert atmosphere.Usually, utilize, contain the air reagent of responding property or the reaction of product basically to well known to a person skilled in the art the air-sensitive synthetic technology.

The B.F2 fragment

The middle portion of compound of the present invention can be represented that this fragment is connected to fragment F1 through the peptide bond that is used to form the F2-F1 midbody by fragment F2.Method through peptide bond or amido linkage coupling compound is well known in the art, and is described in for example peptide: analyze, and synthetic, biology (The Peptides:Analysis, Synthesis, Biology), the 1st volume, volumes such as Gross, Academic press, 1979.The segmental example of F2 is with general formula (E) (P _gBe amino protecting group, R ²Definition herein) provides.In addition, it is well known in the art using Boc or other amino protecting group protection amino group of amino acids.

The formula of amino acid or amino acid derivative (E) compound is commercially available, or is prepared by ordinary method.For example, the preparation of azaserine is generally reset (Hoffman reaction) through Hoffman, utilizes for example l-asparagine, and wherein the acid amides of l-asparagine side chain is converted to amine (it is subsequently by protection).For example, the method for amino acid being implemented the Hoffman rearrangement is being known in the art, and also is provided in the following example.In addition, the preparation method of azaserine is disclosed in Zhang etc., J.Org.Chem., 1997,62,6918-6920.The preparation method of Boc-cyanic acid arginine derivative is disclosed in Wagenaar etc., J.Org.Chem.1993,58,4331-4338.F2 is segmental synthetic, wherein R ²Be-CH ₂CH ₂CH ₂NHC (=NR ⁴) NH-Y ,-CH ₂CONR ⁵R ⁶,-CH ₂NHCONR ⁵R ⁶,-CH ₂NR ⁹R ¹⁰, or-CH (R ⁷) ZR ⁸, further be disclosed in this.Commercially available or the known method preparation by one of skill in the art of F2 fragment.

The C.F3 fragment

Through arbitrary method, such as passing through nucleophilic substitution or addition reaction, another fragment (F3) can be connected to the F2 fragment of F2-F1 midbody, and wherein for example F2 contains nucleophilic reagent (for example, amine), and F3 contains electrophilic reagent (for example, CO, SO ₂Deng) and optional leavings group (for example, halogen, hydroxyl, alkoxyl group, alkyl sulphonyl, aryl sulfonyl etc.).The segmental example of F3 has formula R ^XCOX ^L, R ^XSO ₂X ^L, R ^XNCO, or R ^XHCO, (for example, R ^XBe R in this definition ^A, R ^B, or R ^C, and X ^LBe leavings group).R ^XCOX ^L(for example, work as X ^LWhen being OH) can carry out according to the standard step that peptide bond forms with being connected of F2-F1 midbody, thus the compound of preparation formula F3-F2-F1, wherein F3 is connected via amido linkage with the F2 fragment.In other embodiments, being connected of F3 and F2 adopts by R ^XSO ₂X ^LBe connected with the sulfonamido of F2-F1 midbody prepared in reaction, wherein the amino part on the F2-F1 midbody substitutes R ^XSO ₂X ^LIn X ^LLeavings group.In addition, R ^XNCO and amino partial reaction in the F2-F1 midbody cause urea to be connected (HNCONH-), and after the partial reduction of gained imines, R ^XAmino partial reaction in HCO and the F2-F1 midbody forms amine and is connected.Other methods of attachment also are known and suitable in this area.The F3 fragment can obtain or make by means commonly known in the art from being purchased.

R of the present invention ²Be-(CH ₂) _dCH (R ⁷) NR ⁹R ¹⁰Some compound can be through removing R ¹⁰Amino protecting group forms R ¹⁰Be that H corresponding gone to protect compound and prepared.This de-protected compound can with formula R ^10aX ^LReagent react, R wherein ^10aThe meaning and R ¹⁰Identical, except H, and X ^LBe leavings group, such as halogen or sulfonic acid, or R wherein ^10aAnd X ^LLump together typical example like, reactive alkyl, carbocylic radical or assorted carbocylic radical isocyanic ester, or alkyl, carbocylic radical, assorted carbocylic radical sulfonylisocyanates.For example, the preparation method of embodiment compound D.26 makes the benzyloxycarbonyl of embodiment in D.16.6 go protection to obtain embodiment D.17, and therefrom the N of azaserine is subsequently by acidylate.

The present invention further provides azaserine (for example, the R wherein of formula I ²Be-CH ₂NH ₂) preparation method of compound.Generally speaking, the generation of azaserine group is to remove benzyloxycarbonyl (C (=O) OCH ₂(C ₆H ₅)), the latter is connected to azaserine group (for example, formula I compound, wherein R ²Be-CH ₂NR ⁹R ¹⁰, and R ⁹Be H, and R ¹⁰Be-C (=O) OCH ₂(C ₆H ₅)) on one of them N.The removal of benzyloxycarbonyl is with reductive agent, handles such as hydrogenation reagent.In some embodiments, hydrogenation reagent contains H ₂, choose wantonly in metal catalyst (for example, Pd/C10%) existence use down.Hydrogenation further protonic acid such as HCl in the presence of and containing in the suitable hydrogenation solvent of alcohol for example and/or ether solvents and carrying out.In some embodiments, the hydrogenation solvent contains ether, such as 1, and the 4-diox.In further embodiment, the hydrogenation solvent contains alcohol, such as methyl alcohol.In further embodiment, the hydrogenation solvent contains the mixture of pure and mild ether.For example, embodiment D.17 in, the example for preparing the azaserine compound according to this method is provided.Reaction parameter comprises temperature, pressure, and atmosphere etc. are easy to confirmed by the technician of the field of chemical synthesis, and reaction process is through comprising the for example ordinary method monitoring of NMR.

Therefore, the present invention provides the preparation method of formula (I) compound:

Wherein:

R ²Be-CH ₂NH ₂

Q is-B (OR ¹⁴) ₂, or the ring-type boric acid ester, wherein said ring-type boric acid ester contains 2-20 carbon atom, and optional heteroatoms N, S, or O;

R ¹⁴Be C ₁-C ₄Alkyl, naphthenic base, cycloalkylalkyl, aryl, or aralkyl;

X is R ^AC (=O)-;

R ^ABe C ₁-C ₂₀Alkyl, the optional replacement with R ²⁰

C ₂-C ₂₀Thiazolinyl, the optional replacement with R ²⁰

C ₂-C ₂₀Alkynyl, the optional replacement with R ²⁰

Carbocylic radical, the optional replacement with 1-5R ²¹Or

Assorted carbocylic radical, the optional replacement with 1-5R ²¹

R ²⁰Be selected from:

R ^20aBe C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, or C ₂-C ₂₀Alkynyl; Wherein said alkyl, thiazolinyl, or alkynyl is optional by one or more halogens, C ₁-C ₄Alkyl, aryl, heteroaryl or-NHR ^20bReplace;

R ^20bIt is amino protecting group;

R ^20cIt is optional the replacement with 1-5R ²²Carbocylic radical; Or

The optional replacement with 1-5R ²²Assorted carbocylic radical;

R ²¹Be selected from:

C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, C ₁-C ₂₀Alkoxyl group, C ₁-C ₂₀Thio alkoxy ,-OH ,-CN, halogen, haloalkyl ,-NH ₂,-NH (alkyl) ,-N (alkyl) ₂,-NHC (=O) O-alkyl ,-NHC (=O) alkyl ,-C (=O) O-alkyl ,-C (=O) alkyl ,-S (=O)-alkyl ,-S (=O) ₂-alkyl ,-S (=O)-aryl ,-S (=O) ₂-aryl, the optional replacement with 1-5R ²²Carbocylic radical and optional the replacement with 1-5R ²²Assorted carbocylic radical;

R ²²Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₁₀Thiazolinyl, C ₂-C ₁₀Alkynyl, phenyl, halogen, haloalkyl, alkoxyl group; Thio alkoxy, amino, alkylamino, dialkyl amido, carboxyl; Alkyl-OC (=O)-, alkyl-C (=O)-, aryl-OC (=O)-, alkyl-OC (=O) NH-; Aryl-OC (=O) NH-, alkyl-C (=O) NH-, alkyl-C (O) O-, (alkyl-O) _r-alkyl, and HO-(alkyl-O) _r-alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, alkyl-S (=O)-, alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-; With

R is 2,3,4, or 5;

Comprise:

With R ²Be-CH ₂NH-C (=O) OCH ₂(C ₆H ₅) formula (I) compound and suitable hydrogenation agent be suitable for forming R ²Be-CH ₂NH ₂The condition of formula (I) compound under react for some time, condition is that the hydrogenation agent is to R ²In benzyloxycarbonyl be optionally.

In some embodiments, the hydrogenation agent is at 1 of Pd/C 10% and HCl the H under the 4-diox exists ₂

Boric acid ester/boric acid transforms

Contain boric acid ester, such as the The compounds of this invention of pinane diol ester, can be through the corresponding boric acid of any suitable preparation (B (OH) ₂) method and the hydrolysis of verivate.Hydrolysising condition comprises makes boric acid ester and excess acid, such as the protonic acid contact of HCl.

On the contrary, the esterification of boric acid is to make acid cpd (B (OH) ₂) with pure, contact time enough to produce corresponding ester such as glycol.Esterification can be by acid or base catalysis.

The present invention will describe through specific embodiment in more detail.Following embodiment is provided for the purpose of example, rather than is used for limiting by any way the present invention.Those skilled in the art will readily appreciate that and can change or adjust multiple non-key parameter to produce essentially identical result.

Embodiment

Embodiment A .1

(1R)-the synthesizing of 1-[(6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked borol-2-yls for 3aS, 4S]-3-3-methyl butylamine hydrochloride

Step 1:2-(2-methyl-propyl)-(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked borole

(23.9g, 0.140mol) (15g, the mixture of Anaesthetie Ether 0.147mol) (300ml) was stirring at room 24 hours with 2-methyl-propyl boric acid for (+)-pinine glycol.Mixture is used hexane: 90: 10 mixture wash-outs of ETHYLE ACETATE to anhydrous sodium sulfate drying and through column chromatography purification (silica gel 230-400 order).Obtain limpid oily product (32.6g, yield 94%).

¹H?NMR(DMSO-d ₆)：4.28(1H，dd，J＝8.8Hz，2.0)；2.30(1H，m)；2.18(1H，m)；1.96(1H，t，J＝5.3)；1.86(1H，m)；1.78(1H，set，J＝6.8)；1.68(1H，m)；1.30(3H，s)；1.25(3H，s)；1.01(1H，d)；0.9(6H，d，J＝6.6)；0.81(3H，s)；0.69(2H，m)。

Step 2:2-[(1S)-1-chloro-3-methyl butyl]-(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked borole

Through (35.7ml, anhydrous tetrahydro furan 0.254mol) (60ml) solution add hexane (25.4ml, the 0.254mol) solution, and make temperature rise to-30 ℃ and preparation diisopropylaminoethyl lithium solution of 10.0M butyllithium to Diisopropylamine at-50 ℃.By conduit with solution transfer to the 2-(2-methyl-propyl) of step 1-(3aS, 4S, 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two dislike borole (50g, 0.212mol) and CH ₂Cl ₂(50ml, anhydrous tetrahydrochysene furan 0.848mol) is fed in the solution of (700ml), keeps temperature to be lower than-70 ℃ simultaneously.(339ml, 0.339mol) solution keep internal temperature to be lower than-70 ℃ simultaneously in 30 minutes, to add the Anaesthetie Ether of 1.0M Zinc Chloride Anhydrous then.Reaction mixture-78 ℃ following the stirring 3 hours is warmed to room temperature then.Except that after desolvating, between sherwood oil (1000ml) and 10% aqueous ammonium chloride solution (800ml), distribute residue through rotary evaporation.Further use sherwood oil (300ml) to extract water.The organic phase that merges is to anhydrous sodium sulfate drying and concentrated.Acquisition contain about 9%mol/mol starting substance ( ¹H-NMR) brown oily product (59.0g, yield 98%), and need not be further purified and be used for subsequent step.

¹H?NMR(DMSO-d ₆)：4.43(1H，dd，J＝8.8，1.8)；3.59(1H，m)；2.33(1H，m)；2.21(1H，m)；2.01(1H，m)；1.88(1H，m)；1.84-1.55(5H，m)；1.34(3H，s)；1.26(3H，s)；1.09(1H，J＝10.1)；0.9(3H，d，J＝6.8)；0.87(3H，d，J＝6.4)；0.82(3H，s)。

Step 3:N, two (trimethyl silyl)-(the 1R)-1-of N-(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methylbutylamine

To the rough 2-of step 2 [(1S)-1-chloro-3-methyl butyl]-(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked borole (59.0g, purity 91%; 0.189mol) oxolane (580ml) solution in add the oxolane of two (trimethyl silyl) lithium amides of 1.0M in 30 minutes (189ml, 0.189mol) solution cool off at-78 ℃ simultaneously.Reaction mixture slowly is warmed up to ambient temperature overnight.Except that desolvating, absorb residue through rotary evaporation with anhydrous hexane (800ml).The suspension that obtains filters through cake (celite cake) in the plug then and removes solid stirring at room 2 hours, and (3 * 100ml) wash this cake with anhydrous hexane.Leach thing and produced the product (79g) that brown buttery purity is share with in fact quantitative yield by concentrated.This product need not to be further purified step and is used for next step.

¹H?NMR(DMSO-d ₆)：4.33(1H，dd，J＝1.5Hz，8.6)；2.58(1H，m)；2.29(1H，m)；2.18(1H，m)；1.95(1H，t，J＝5.9)；1.85(1H，m)；1.9-1.55(3H，m)；1.31(3H，s)；1.24(3H，s)；1.17(1H，m)；1.01(1H，d，J＝10.6)；0.85(3H，d，J＝6.6)，0.83(3H，d，J＝6.6)；0.80(3H，s)；0.08(18H，s)。

Step 4: (1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-3-methyl butylamine hydrochloride

To the thick N of step 3, N-two (trimethyl silyl)-(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-3-methylbutylamine (79g; 0.193mol) the solution of mixture of dioxanes (100ml) and Anaesthetie Ether (200ml) in add the dioxanes of 4N hydrochloric acid (193ml, 0.772mol) solution cool off at 0 ℃ simultaneously.Then at this mixture of stirring at room 4 hours and concentrated.Absorb residue and add Anaesthetie Ether (48ml, 0.096mol) solution of 2M hydrochloric acid with anhydrous hexane (500ml).Mixture stirred 1 hour at 0 ℃, concentrated then.Absorb residue with anhydrous hexane (500ml), the suspension that obtains is in stirred overnight at room temperature.Solid collected by filtration and vacuum-drying obtain 38.1g product (yield 66%).Obtain product (4.13g, yield 7%) once more from mother liquor.

¹H?NMR(DMSO-d ₆)：7.85(3H，br)；4.45(1H，dd，J＝9.2Hz)；2.78(1H，m)；2.34(1H，m)；2.21(1H，m)；2.01(1H，t，J＝5.3)；1.89(1H，m)；1.82-1.65(2H，m)；1.49(1H，m)；1.38(3H，s)；1.27(3H，s)；1.12(1H，d，J＝1.12)；0.87(6H，d，J＝6.6)；0.83(3H，s)。

Embodiment A .2

2-(2-methyl-propyl)-(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium 4,6-methylene radical-1,3,2-benzo dioxaborole's is alternately synthetic

Step 1:2-(1-methyl ethoxy)-(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked borole.

To (1S, 2S, 3R, 5S)-(+)-pinine glycol (50.0g slowly adds three isopropoxy borines in the solution of anhydrous tetrahydro furan 0.293mol) (350ml), simultaneously 0 ℃ with nitrogen stirring down.After 2 hours, shift out solvent through rotary evaporation.The oily residue is dissolved in the hexane (150ml) again, and filters this solution to remove the white solid of very small amount.Filtrating concentrates behind rotary evaporation, obtains limpid oily product (62.6g, yield 90%).

¹H?NMR(DMSO-d6)：4.31-4.20(2H，m)；2.34-2.16(2H，m)；1.96(1H，t，J＝5.5)；1.90-1.85(1H，m)；1.74-1.67(1H，m)；1.32(3H，s)；1.31(1H，d，J＝7.6)；1.25(3H，s)；1.14(3H，d，J＝6.1)；1.13(3H，d，J＝6.1)；0.81(3H，s)。

Step 2:2-(2-methyl-propyl)-(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked borole.

The 2-(1-methyl ethoxy) that obtains to step 1-(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked borole, and (62.6g is in anhydrous tetrahydro furan 0.263mol) (330ml) solution; In 1 hour, dropwise add 2M isobutyl group magnesium bromide Anaesthetie Ether (131.5ml, 0.263mol) solution, simultaneously-78 ℃ with nitrogen stirring down.Then, let mixture heat, shift again in the mixture of 2N sulfuric acid (150ml) and Di Iso Propyl Ether (250ml) to room temperature.Stir after 10 minutes, add the saturated solution of NaCl, and separating layer.With salt solution (100ml) washing organic phase, to dried over sodium sulfate and concentrated.Through column chromatography (silica gel), with the hexane wash-out of 5% Anaesthetie Ether, purifying residue.Obtain limpid buttery product (38.45g, yield 62%).

Embodiment B .1

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl-carbamic acid 1,1-dimethyl ethyl ester

Method A:HOAt/HATU

To BocNH (NO ₂) (15.7g adds HATU (O-(7-azepine benzo triazol-1-yl)-1,1,3,3-tetramethyl-uronium hexafluorophosphate to ArgOH in dry DMF 49.3mmol) (100ml) solution; 18.7g, 49.3mmol) and HOAt (1-hydroxyl-7-azepine benzotriazole; 6.71g, 49.3mmol).Mixture be cooled to 0 ℃ and add N-methylmorpholine (13.6ml, 0.123mol).After 10 minutes, (1R)-1-of interpolation embodiment A .1 [(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5 trimethyls-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yls]-the 3-3-methyl butylamine hydrochloride (12.4g, 41.1mmol).Remove cooling bath and with mixture stirring at room 4.5 hours.Mixture is with ETHYLE ACETATE (800ml) dilution, with 2% citric acid solution (2 * 150ml), 2%NaHCO ₃Solution (2 * 150ml) with 2%NaCl solution (2 * 150ml) washing.Further use ETHYLE ACETATE (150ml) aqueous phase extracted.The organic phase that merges is to dried over sodium sulfate and concentrated.The oily residue that obtains heavily is dissolved in ETHYLE ACETATE (500ml) and washs this solution with cold water (200ml).Further use ETHYLE ACETATE (150ml) aqueous phase extracted.The organic phase that merges is to dried over sodium sulfate and concentrated.Residue is dissolved in Anaesthetie Ether (100ml) and solution is slowly added in the hexane (600ml) under stirring.White solid (43.4g) is collected in filtration and through column chromatography purification, begin with 50: 50 hexanes: ethyl acetate mixture is used eluent ethyl acetate then.Concentrate the level that contains product and divide, residue is dissolved in the Anaesthetie Ether (100ml) and under agitation the solution that obtains is slowly added in the hexane (600ml).Filter and collect white solid (15.2g, yield 66%).

Method B:IBCF

To BocNH (NO ₂) ArgOH (and 5.82g, add in anhydrous methylene chloride 18.2mmol) (100ml) suspension N-methylmorpholine (2.0ml, 18.2mmol).Mixture is cooled to-15 ℃, add then isobutyl chloroformate (2.37ml, 18.2mmol).Mixture stirs at-15 ℃ and added (1R)-1-[(3aS, 4S, the 6S that embodiment A .1 obtains in 10 minutes then; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-3-3-methyl butylamine hydrochloride (5.0g; 16.6mmol), immediately add in addition N-methylmorpholine (2.0ml, 18.2mmol).Reaction mixture stirred 1.5 hours at-15 ℃, was warmed to room temperature then and at ETHYLE ACETATE (150ml), distribution between water (150ml) and the 0.1N hydrochloric acid (10ml).Use NaHCO ₃Saturated solution washing organic phase, to anhydrous sodium sulfate drying and concentrate.Provide 3 batches of purity suitable product (5.03g, yield 54%) through crystallization purifying oily residue from ETHYLE ACETATE.

¹H?NMR(DMSO-d ₆)：8.80(1H，br)；8.50(1H，br)，7.87(2H，br)；7.01(1H，d，J＝7.9)，4.07(1H，dd，J＝7.9)；4.0(1H，m)；3.12(2H，m)；2.55(1H，m)；2.2(1H，m)；2.01(1H，m)；1.83(1H，t，J＝5.1)；1.78(1H，m)；1.74-1.44(7H，m)；1.38(9H，s)；1.33(1H，d，J＝10.3)；1.24(5H，s)；1.22(3H，s)；0.84(6H，d，J＝6.6)；0.81(3H，s)。

Embodiment B .2

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-the 2-hydroxypropyl]-carbamic acid 1,1-dimethyl ethyl ester

Be dissolved in dry DMF (30ml) under Boc-L-Threonine (870mg, 3.97mmol, the 1.2 equivalents) room temperature.In this solution, adding TBTU (N, N, N ', N '-tetramethyl--O-(benzotriazole-1-yl) uronium a tetrafluoro borate (1270mg, 3.97mmol, 1.2 equivalents), and at 0-5 ℃ of cooling mixture.Then, (the 1R)-1-[(3aS, the 4S that add NMM (0.9ml, 8.27mmol, 2.5 equivalents) and embodiment A .1; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-3-3-methyl butylamine hydrochloride (1000mg, 3.3mmol, 1 equivalent).Stirred the mixture under the room temperature 16 hours, again with ETHYLE ACETATE (100ml) extraction, with following solution washing: Hydrocerol A 2% (50ml), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml).Organic solution is filtered and vapourisation under reduced pressure, to obtain 1290mg hyaloid solid anhydrous sodium sulfate drying.Yield 84.3%.

M.p.25℃-30℃

¹H?NMR(DMSO-d ₆)：8.88(1H，br)；6.49(1H，d，J＝8.4Hz)；4.88(1H，d，J＝5.8)；4.05(1H，dd)；3.93(1H，m)；(1H，m)；2.51(1H，m)；2.19(1H，m)；2.01(1H，m)；1.83(1H，t，J＝5.9)，1.78(1H，m)；1.68(1H，m)；1.62(1H，m)；1.39(9H，s)；1.34(1H，d，J＝10.0)；1.24(3H，s)；1.22(3H，s)；1.06(3H，d，J＝6.4)；0.85(6H，d，J＝6.4)；0.80(3H，s)。

Embodiment B .3

Other midbody compounds

From suitable midbody and follow Embodiment B .1 and B.2 described in arbitrary method, prepare hereinafter mesosome.

(2S)-2-[(1,1-dimethyl ethoxy carbonyl) amino]-5-urea groups pentanamide, N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]

Chirality

¹H?NMR(DMSO-d ₆)：8.85(1H，br)；7.01(1H，d，J＝8.0Hz)；5.9(1H，t，J＝5.7)；5.36(2H，br)；4.03(2H，m)；2.93(2H，m)；2.19(1H，m)；2.0(1H，m)；1.83(1H，t，J＝5.3)；1.78(1H，m)；1.68(1H，m)；1.62(1H，m)；1.52(2H，m)；1.38(9H，s)；1.33(1H，d，J＝9.9)；1.24(3H，s)；1.22(2H，s)；0.86(3H，d，J＝6.6)；0.84(3H，d，J＝6.6)；0.80(3H，s)。

(2S)-3-(amino carbonyl)-2-[(1,1-dimethyl ethoxy carbonyl) amino] propionamide, N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]

¹H?NMR(DMSO-d ₆)：8.74(1H，br)；7.28(1H，br)；6.95(2H，m)；4.36(1H，m)；4.07(1H，m)；2.55(1H，m)；2.38(2H，m)；2.2(1H，m)；2.02(2H，m)；1.84(1H，t，J＝5.5)；(1H，m)；1.79(1H，m)；1.68(1H，m)；1.63(1H，m)；1.38(9H，s)；1.33(1H，d，J＝10)；1.24(3H，s)；1.22(2H，s)；0.85(3H，d，J＝6.4)；0.83(3H，d，J＝6.4)；0.81(3H，s)。

The carbamic acid benzyl ester, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-the 2-hydroxypropyl].

Chirality

M.p.57-60℃。 ¹H?NMR(DMSO-d6)：8.66(1H，s)；7.40-7.29(5H，m)；7.09(1H，d，J＝8.75)；5.06(2H，s)；4.90(1H，J＝5.68)；4.11-3.99(2H，m)；3.91-3.77(1H，m)；2.58-2.53(1H，m)；2.26-2.14(1H，m)；2.07-1.97(1H，s)；1.84(1H，t，J＝5.52)；1.81-1.75(1H，m)；1.73-1.58(2H，m)；1.33(2H，d，J＝10.1)；1.27-1.20(7H，m)；1.06(3H，t，J＝6.27)；0.91-0.79(9H，m)。

Embodiment B .4

(2S)-2-[(1,1-dimethyl ethoxy carbonyl) amino]-3-[(4-toluyl) amino] propionamide, N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-

Under nitrogen, with embodiment (2S)-2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-[(4-methyl benzoyl) amino]-propionic acid (650mg G.6; 2mmol, 1.2 equivalents) be dissolved in the dry DMF (15ml), and at room temperature add TBTU (640mg; 2mmol, 1.2 equivalents).Mixture cools off in 0-5 ℃ with ice bath, and adds (1R)-1-[(3aS of NMM (0.55ml, 5mmol, 2.5 equivalents) and embodiment A .1; 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-3-3-methyl butylamine hydrochloride (500mg, 1.65mmol, 1 equivalent).The mixture stirred overnight is poured in the water (200ml), and extracts with ETHYLE ACETATE (100ml).With following solution washing organic layer: Hydrocerol A 2% (20mL), sodium hydrogencarbonate 2% (20ml), NaCl2% (20ml).Organic solution is filtered and evaporation, to obtain 740mg hyaloid solid (quantitative yield) anhydrous sodium sulfate drying.

¹H?NMR(DMSO-d ₆)8.76(1H，br)；8.28(1H，t，J＝5.31Hz)；7.71(2H，d，J＝7.9)；7.26(2H，d，J＝7.9)；6.97(1H，d，J＝8.0)；4.27(1H，m)：4.07(1H，dd，J＝8.2，1.5)；3.48(2H，m)，2.58(1H，m)；2.35(3H，s)；2.19(1H，m)；2.02(1H，m)；1.83(1H，t，J＝4.9)；1.78(1H，m)；1.62(2H，m)；1.35(12H，m)；1.24(3H，s)；1.23(3H，s)；0.82(3H，d)；0.80(3H，d)；0.78(3H，s)。

Embodiment B .5

2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(caproyl is amino)-propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl 4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]

Under nitrogen, embodiment 2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(caproyl is amino) propionic acid (300mg, 1mmol, 1.2 equivalents) G.7 is dissolved in the dry DMF (25ml), add TBTU (318mg, 1mmol, 1.2 equivalents) under the room temperature.Mixture cools off at 0-5 ℃ with ice bath, and adds (1R)-1-[(3aS of NMM (0.27ml, 2.47mmol, 2.47 equivalents) and embodiment A .1; 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-3-3-methyl butylamine hydrochloride (250mg, 0.82mmol, 1 equivalent).Mixture stirred 3 hours, was poured in the water (150ml), and extracted with ETHYLE ACETATE (100ml).With following solution washing organic layer: Hydrocerol A 2% (50mL), sodium hydrogencarbonate 2% (50ml), NaCl2% (50ml).Organic layer filters and evaporation anhydrous sodium sulfate drying, obtains 450mg hyaloid solid.Quantitative yield.

Analytical data:

¹H?NMR(DMSO-d ₆).

δ _H：8.71(1H，br?d，J＝2.6Hz)；7.73(1H，br?t，J＝5.9Hz)；6.81(1H，d，J＝8.2)；4.10(2H，m)；3.24(2H，m)；2.56(1H，m)；2.19(1H，m)；2.03(3H，m)；1.83(1H，t，J＝5.5)；1.78(1H，m)；1.64(2H，m)；1.47(2H，m)；1.36(9H，s)；1.4-1.15(9H，m)；1.24(3H，s)；1.21(3H)；0.83(9H，m)；0.79(3H，s)。

Embodiment B .6

2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(4-fluorine sulfonamido) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]

Under nitrogen, with embodiment 2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(4-fluorine sulfonamido) propionic acid (1.39g G.8; 3.83mmol, 1.2 equivalents) be dissolved in the dry DMF (20ml), and add TBTU (1.23g under the room temperature; 3.83mmol, 1.2 equivalents).Mixture cools off down at 0-5 ℃ with ice bath, and adds (1R)-1-[(3aS of NMM (1ml, 9.57mmol, 3 equivalents) and embodiment A .1; 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-3-3-methyl butylamine hydrochloride (0.96g, 3.19mmol, 1 equivalent).Mixture stirred 2 hours, was poured in the water (200ml), and extracted with ETHYLE ACETATE (100ml).With following solution washing organic layer: Hydrocerol A 2% (50mL), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml).Organic solution is to anhydrous sodium sulfate drying, filters and with the Anaesthetie Ether evaporation, obtains the 1.5g white solid.Yield 77%.

Analytical data:

¹H?NMR(DMSO-d ₆)。

δ _H：8.54(1H，d，J＝2.9Hz)；7.91(2H，m)；7.75(1H，t，J＝5.9)；7.50(2H，t，J＝8.8)；6.83(1H，d，J＝8.4)；4.19(1H，br?d，J＝8.2)；4.14(1H，m)；3.01(2H，m)；2.69(1H，m)；2.25(1H，m)；2.09(1H，m)；1.90(1H，t，J＝5.7)；1.85(1H，m)；1.8-1.6(2H，m)；1.5-1.2(5H，m)；1.43(9H，s)；1.29(6H，s)；0.89(6H，d，J＝6.4)；0.86(3H，s)。

Embodiment B .7

2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(3,4-Dimethoxyphenyl acetylamino) propionamide; N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]

Under nitrogen, with embodiment 2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3 G.9; 4-Dimethoxyphenyl kharophen)-propionic acid (0.73g, 1.90mmol, 1.2 equivalents) is dissolved in the dry DMF (20ml); Add TBTU (0.61g, 1.90mmol, 1.2 equivalents) under the room temperature.Mixture 0-5 ℃ of cooling, and adds (1R)-1-[(3aS of NMM (0.52ml, 4.7mmol, 2.5 equivalents) and embodiment A .1 with ice bath; 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-3-3-methyl butylamine hydrochloride (0.47g, 1.6mmol, 1 equivalent).Mixture stirred 2 hours, was poured in the water (200ml) and with ETHYLE ACETATE (100ml) to extract.With following solution washing organic layer: Hydrocerol A 2% (50mL), sodium hydrogencarbonate 2% (50ml), NaCl2% (50ml).Organic solution is to anhydrous sodium sulfate drying, filters and with the Anaesthetie Ether evaporation, obtains the 0.95g crude product, behind silica gel column chromatography purifying (eluent ETHYLE ACETATE), obtains the 0.3g white foam.Yield 30%.Analytical data: TLC silica gel (eluent ETHYLE ACETATE 100%, R.f.=0.50)

¹H?NMR(MSO-d6)。

δ _H：8.69(1H，d，J＝2.6Hz)；7.90(1H，t，J＝5.7)；6.85(2H，m)；6.74(1H，dd，J＝1.5，8.1)；6.85(3H，m)；4.12(2H，m)；3.73(3H，s)；3.72(3H，s)；3.34(2H，s)；3.31(2H，m)；2.58(1H，m)；2.20(1H，m)；2.03(1H，m)；1.85(1H，t，J＝5.3)；1.79(1H，m)；1.66(2H，m)；1.38(9H，s)；1.40-1.15(3H，m)；1.25(3H，s)；1.23(3H，s)；0.83(6H，d，J＝6.6)；0.81(3H，s)。

Embodiment B .8

2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(3-phenyl urea groups) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]

Under nitrogen, with embodiment 2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3-phenyl urea groups) propionic acid (0.41g G.10; 1.26mmol, 1.2 equivalents) be dissolved in the dry DMF (20ml), and at room temperature add TBTU (0.40g; 1.26mmol, 1.2 equivalents).Mixture cools off down at 0-5 ℃ with ice bath, and adds (1R)-1-[(3aS of NMM (0.346ml, 3.15mmol, 2.5 equivalents) and embodiment A .1; 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-3-3-methyl butylamine hydrochloride (0.31g, 1mmol, 1 equivalent).Mixture stirred 2 hours, was poured in the water (200ml) and with ETHYLE ACETATE (100ml) to extract.Organic layer is with following solution washing: Hydrocerol A 2% (50mL), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml).Organic solution is to anhydrous sodium sulfate drying, filters and with Anaesthetie Ether (50ml) evaporation, obtains the 0.58g white solid.Yield 96.6%.

Analytical data: TLC silica gel (eluent ETHYLE ACETATE 100%, R.f.=0.47), m.p.128-130 ℃.

¹H?NMR(DMSO-d ₆)。

δ _H：8.79(1H，d，J＝2.7Hz)；8.69(1H，s)；7.38(2H，d，J＝7.9)；7.22(2H，t，J＝8.1)；7.00(1H，d，J＝8.1)；6.90(1H，t，J＝7.3)；6.16(1H，t，J＝5.7)；4.12(2H，m)；3.45(1H，m)；3.17(1H，m)；2.60(1H，m)；2.21(1H，m)；2.04(1H，m)；1.85(1H，t，J＝5.3)；1.79(1H，m)；1.66(2H，m)；1.38(9H，s)；1.40-1.15(3H，m)；1.26(3H，s)；1.23(3H，s)；0.84(6H，d，J＝6.6)；0.81(3H，s)。

Embodiment B .9

Synthesizing of other compounds

Follow the method for Embodiment B .4-B.8, by (1R)-1-[(3aS, the 4S of embodiment A .1; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yls]-3-3-methyl butylamine hydrochloride and embodiment G.11, G.12 and intermediate prepared in reaction following compounds G.13.

Embodiment B .10

Carbamic acid 1,1-dimethyl ethyl ester, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 1-methyl butyl] amino] carbonyl]-methyl

According to the step of Embodiment B .1 method B, from (1R)-1-[(3aS, the 4S of embodiment A .1; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-the 3-3-methyl butylamine hydrochloride is initial with N-(1, the 1-dimethyl ethoxy carbonyl) glycine that is purchased, and prepares this compound.

¹H-NMR(DMSO-d6)：8.84(1H，s)；7.08(1H，t，J＝5.93Hz)；4.06(1H，d，J＝7.48Hz)；3.67(2H，t，J＝5.32Hz)；2.60-2.48(1H，m)；2.24-2.16(1H，m)；2.06-1.96(1H，m)；1.84(1H，t，J＝5.50Hz)；1.82-1.76(1H，m)；1.74-1.58(2H，m)；1.39(10H，bs)；1.23(9H，d，J＝8.18Hz)；0.87-0.83(6H，m)；0.82(3H，bs)。

Embodiment C .1

(2S)-2-amino-5-[[imino group (nitro amino) methyl] amino] pentanamide, N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]; Hydrochloride

Method A

To the carbamic acid 1 of Embodiment B .1,1-dimethyl ethyl ester, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-(4.04g; 7.06mmol) the solution of mixture of dioxanes (40ml) and Anaesthetie Ether (7ml) in, add the dioxanes (15ml) of 4N HCl, simultaneously 0 ℃ of cooling.Let reaction mixture heat, and stirred in addition 4 hours to room temperature.Remove solvent through rotary evaporation, handle residue with Anaesthetie Ether (50ml), and at room temperature stirred the mixture 3 days.Filter and collect the gained solid, obtain 3.18g pure products (yield 90%).

Method B

The carbamic acid 1 of Embodiment B .1,1-dimethyl ethyl ester, N-[(1S)-1-[[[(1R)-1-[(3aS; 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-amino]-carbonyl]-4-[[imino group (nitro amino)-methyl]-amino] butyl]-(3g 5.3mmol) is dissolved in Et ₂Among the O (40mL), and 0 ℃ with nitrogen under, dropwise add the Et of about 10%HCl ₂O (20mL) solution.Let reaction mixture heat, and stirred in addition 5 hours to room temperature.Topple over solvent, residue is with Et ₂O (20mL) washed twice, vacuum-drying obtains the title compound (2.43g, yield 91%) of white powder.

¹H?NMR(DMSO-d ₆)：8.56(2H，br)；8.22(3H，br)；7.97(2H，br)；4.28(1H，dd，J＝8.6Hz，2.01)；3.77(1H，m)；3.04(1H，m)；2.28(1H，m)；2.11(2H，m)，1.92(1H，t，J＝5.5)；1.83(1H，m)；1.79-1.59(4H，m)；1.59-1.37(3H，m)；1.31(4H，s)；1.24(3H，s)；1.19(1H，d，J＝10.4)；0.88(3H，d，J＝6.0)；0.86(3H，d，J＝6.0)；0.81(3H，s)。

Embodiment C .2

Boric acid, [(1R)-1-[[(2S)-and 2-amino-5-[[imino-(nitro amino) methyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl], hydrochloride

Under nitrogen and 0 ℃, with the N-of Embodiment B .1 [(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yls]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-carbamic acid 1, (3.1g 5.48mmol) carefully is dissolved in the HCl 37% of 20mL to 1-dimethyl ethyl ester; Allow the gained mixture heat to room temperature, and stir overnight.Reaction mixture is with Et ₂The O washing is up to removing pinine glycol fully; The aqueous solution is concentrated into drying, and dry under vacuum, obtains the title compound of 1.82g (4.93mmol, yield 90%), need not to be further purified subsequent use.

¹H?NMR(DMSO+D ₂O+TFA)：3.78(m，1H)；3.19(m，2H)；3.09(m，1H)；1.71(m，2H)；1.70-1.48(m，3H)；1.49-1.23(m，2H)；0.89(d，J＝5.8Hz，3H)；0.88(d，J＝5.8Hz，3H)。

Embodiment C .3

Synthesizing of other midbodys

From suitable midbody, and follow the arbitrary step described in the Embodiment C .1, prepare following midbody:

(2S, 3R)-2-amino-3-maloyl group amine, N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-, hydrochloride

¹H?NMR(DMSO-d ₆)δ _H：8.62(1H，d，J＝5.0Hz)；8.17(3H，d，J＝3.5)；4.28(1H，dd，J＝8.8，1.8)；3.78(1H，m)；3.52(1H，m)；3.00(1H，m)；2.28(1H，m)；2.10(1H，m)；1.92(1H，t，J＝5.7)；1.84(1H，m)；1.75-1.62(2H，m)；1.43(1H，m)；1.31(3H，s)；1.25(3H，s)；1.22(1H，d，J＝10.6)；1.14(3H，d，J＝6.2)；0.88(3H，d，J＝6.4)；0.86(3H，d，J＝6.4)；0.81(3H，s)。

(2S)-2-amino-5-urea groups pentanamide, N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]; Hydrochloride

Chirality

¹H?NMR(DMSO-d ₆)8.51(1H，d，J＝5.1Hz)；8.17(3H，br)；6.1(1H，br)；4.27(1H，dd，J＝8.6Hz，1.8)；3.73(1H，m)；2.99(1H，m)；2.94(2H，t)；2.27(1H，m)；2.10(1H，m)，1.92(1H，t，J＝5.5)；1.82(1H，m)；1.75-1.15(9H，m)；1.30(3H，s)；1.23(3H，m)；0.87(3H，d，J＝6.0)；0.85(3H，d，J＝6.0)；0.80(3H，s)。

(2S)-2-amino-3-carbamoyl propionamide, N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]; Hydrochloride

Chirality

¹H-NMR(DMSO-d6)：8.46-8.41(1H，m)；8.06(3H，bs)；7.67(1H，s)；7.26(1H，s)；4.30-4.25(1H，m)；4.08-4.02(1H，m)；2.96(1H，m)；2.60-2.52(1H，m)；2.36-2.24(1H，m)；2.20-2.10(1H，m)；1.95(1H，t，J＝5.5)；1.88-1.83(1H，m)；1.75-1.60(2H，m)；1.46-1.36(1H，m)；1.32(3H，s)；1.30-1.18(6H，m)；0.86(6H，t，J＝6.7)；0.82(3H，s)。

The 2-amino acetamide, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 1-methyl butyl]; Hydrochloride

Chirality

¹H-NMR(DMSO-d6)：8.50(1H，s)；8.20(3H，bs)；4.29(1H，d，J＝7.70Hz)；3.15(2H，bs)；3.05(1H，s)；2.36-2.24(1H，m)；2.20-2.10(1H，m)；1.95(1H，t，J＝5.38Hz)；1.85(1H，s)；1.75-1.60(2H，m)；1.50-1.38(1H，m)；1.35-1.30(3H，m)；1.28-1.25(4H，m)；1.24-1.17(1H，m)；0.86(6H，t，J＝5.94Hz)；0.84(3H，s)。

Embodiment C .4

(2S)-2-amino-3-[(4-toluyl) amino] propionamide, N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl 4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-, hydrochloride.

With (2S)-2-[(1,1-dimethyl ethoxy carbonyl) amino]-3-[(4-methyl benzoyl)-amino]-propionamide of Embodiment B .4, and N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-(740mg; 1.65mmol, 1 equivalent) and be dissolved in 1,4-dioxanes (20ml).In this solution, add 1 of HCl 4N, 4-diox (5ml, 19.8mmol, 12 equivalents), this solution is stirred overnight at room temperature.Decompression goes down to desolventize, and obtains 800mg hyaloid solid (quantitative yield).

¹H?NMR(DMSO-d ₆)8.63(1H，d，J＝5.5Hz)；8.38(1H，t，J＝8.4Hz)；8.34(3H，br)；7.80(2H，t，J＝8.2)；7.28(2H，d，J＝8.2Hz)；4.15(1H，dd，J＝8.8，1.8)；4.02(1H，br)；3.66(1H，m)；3.55(1H，m)；2.99(1H，m)；2.35(3H，s)；2.19(1H，m)；2.06(1H，m)；1.86(1H，t，J＝5.7)；1.80(1H，m)；1.64(2H，m)；1.41(1H，m)；1.33-1.19(2H，m)；1.27(3H，s)，1.21(3H，s)；1.16(1H，d，J＝10.6)；0.82(3H，d)；0.80(3H，d)；0.78(3H，s)。

Embodiment C .5

2-S-amino-3-(hexanoyl is amino)-propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], hydrochloride

With 2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(caproyl is amino) propionamide of Embodiment B .5, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], (450mg; 0.8mmol, 1 equivalent) and be dissolved in 1,4-dioxanes (15ml).In this solution, add 1 of HCl 4N, 4-diox (2.45ml, 0.98mmol, 12 equivalents), and at room temperature stir this solution.Decompression goes down to desolventize, and obtains 400mg hyaloid solid.Quantitative yield.

Analytical data: ¹H NMR (DMSO-d ₆).

δ _H：8.54(1H，d，J＝5.3Hz)；8.18(3H，br)；7.74(1H，t，J＝5.7)；4.29(1H，dd，J＝1.8，8.8)；3.83(1H，m)；3.40(2H，m)；3.00(1H，m)；2.29(1H，m)；2.11(1H，m)；2.08(2H，t，J＝7.5)；1.93(1H，t，J＝5.5)；1.84(1H，m)；1.75-1.15(11H，m)；1.32(3H，s)；1.24(3H，s)；0.86(3H，d，J＝6.6)；0.84(3H，d，J＝6.6)；0.81(3H，s)。

Embodiment C .6

2-S-amino-3-(4-fluorine sulfonamido) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], hydrochloride

With 2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(4-fluorine sulfonamido) propionamide of Embodiment B .6, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], (0.7g; 1.14mmol, 1 equivalent) and be dissolved in 1,4-dioxanes (20ml).In this solution, add 1 of HCl4N, 4-diox (3.4ml, 13.68mmol, 12 equivalents), and at room temperature stir this solution and spend the night.Decompression goes down to desolventize, and obtains the 440mg white solid.Yield 71%.Analytical data:

¹H?NMR(DMSO-d ₆)。

δ _H：8.54(1H，d，J＝5.5Hz)；8.26(3H，br)；7.89(3H，m)；7.48(3H，t，J＝8.8)；4.26(1H，dd，J＝1.3，8.6)；3.84(1H，m)；3.06(2H，m)；2.97(1H，m)；2.25(1H，m)；2.03(1H，m)；1.83(2H，m)；1.64(2H，m)；1.42(1H，m)；1.35-1.15(3H，m)；1.28(3H，s)；1.22(3H，s)；1.11(1H，d，J＝10.8)；0.85(6H，m)；0.80(3H，s)。

Embodiment C .7

2-S-amino-3-(3,4-Dimethoxyphenyl acetylamino) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl 4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], hydrochloride

With 2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(3,4-Dimethoxyphenyl acetylamino)-propionamide of Embodiment B .7, N-[(1S)-1-[[(1R)-1-[(3aS; 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4.6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], (0.3g; 0.47mmol, 1 equivalent) and be dissolved in 1,4-dioxanes (20ml).In this solution, add 1 of HCl 4N, 4-diox (1.43ml, 5.71mmol, 12 equivalents), and at room temperature stir this solution and spend the night.Decompression goes down to desolventize, and adds Anaesthetie Ether, obtains the 230mg white solid after the evaporation.Yield 85%.

Analytical data: ¹H NMR (DMSO-d ₆).

δ _H：8.57(1H，br)；8.12(3H，br)；7.91(1H，t，J＝5.7Hz)；6.86(2H，m)；6.76(1H，dd，J＝1.8，8.2)；4.26(1H，br?d，J＝7.3)；3.82(1H，m)；3.72(3H，s)；3.71(3H，s)；3.36(2H，s)；3.34(2H，m)；2.99(1H，m)；2.26(1H，m)；2.10(1H，m)；1.92(1H，t，J＝5.3)；1.83(1H，m)；1.67(2H，m)；1.45-1.15(3H，m)；1.31(3H，s)；1.23(3H，s)；0.86(3H，d，J＝6.6)；0.84(3H，d，J＝6.6)；0.80(3H，s)。

Embodiment C .8

2-S-amino-3-(3-phenyl-urea groups)-propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], hydrochloride.

With 2-S-[(1,1-dimethyl ethoxy carbonyl) amino]-3-(3-phenyl urea groups) propionamide of Embodiment B .8, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl], (0.58g; 0.1mmol, 1 equivalent) and be dissolved in 1,4-dioxanes (25ml).In this solution, add 1 of HCl 4N, 4-diox (3ml, 12.1mmol, 12 equivalents), and at room temperature stir this solution and spend the night.Decompression goes down to desolventize, and adds Anaesthetie Ether, obtains the required product of 0.52g after the evaporation.Yield 100%.

Analytical data:

¹H?NMR(DMSO-d ₆)。

δ _H：8.82(1H，s)；8.59(1H，d，J＝5.7Hz)；8.18(3H，br)；7.40(2H，d，J＝7.9)；7.22(2H，t，J＝8.1)；6.90(1H，t，J＝7.3)；6.31(1H，t，J＝5.7)；4.26(1H，dd，J＝1.5，8.6)；3.89(1H，m)；3.48(1H，m)；3.36(1H，m)；3.01(1H，m)；2.24(1H，m)；2.10(1H，m)；1.92(1H，t，J＝5.3)；1.82(1H，m)；1.67(2H，m)；1.50-1.15(3H，m)；1.31(3H，s)；1.21(3H，s)；0.85(3H，d，J＝6.6)；0.84(3H，d，J＝6.6)；0.79(3H，s)。

Embodiment C .9

Synthesizing of other compounds

Follow the step of Embodiment C .4-C.8, from the intermediate preparation following compounds of Embodiment B .9.

Embodiment D.1

Decyl amide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-

To capric acid (0.84g, in dry DMF 4.83mmol) (30ml) solution, add HATU (1.84g, 4.83mmol) and HOAt (0.66g, 4.83mmol).Stir under the room temperature after 15 minutes, at 0 ℃ of this mixture of cooling, and the adding N-methylmorpholine (1.33ml, 12.1mmol).After 20 minutes, add (2S)-2-amino-5-[[imino group (nitro amino) methyl] amino] pentanamide of Embodiment C .1, and N-[(1R)-1-[(3aS; 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-hydrochloride (2.2g, 4.03mmol).Let mixture heat, and stirred 5 hours, dilute then with ETHYLE ACETATE (150ml) to room temperature, with 2% citric acid solution (2 * 100ml), 2%NaHCO ₃Solution (2 * 100ml) and 2%NaCl solution (2 * 100ml) washing.Organic phase is to dried over sodium sulfate and concentrated.Residue is through column chromatography purification, with AcOEt/n-hexanes mixtures from 80/20 to 100/0 wash-out.The gained solid grinds with Anaesthetie Ether, and filter and collect, and dry under vacuum, obtain 1.8g product (yield 72%).

M.P.89-94℃

Ultimate analysis calculated value: C 59.99% H 9.26% N 13.54%

Measured value: C 59.47% H 9.51% N 13.42%

¹H?NMR(DMSO-d ₆)：8.82(1H，d，J＝2.7Hz)；8.53(1H，br)；7.99(1H，d，J＝8.05)；7.88(2H，br)；4.33(1H，m)；4.08(1H，dd，J＝1.6，8.6)；3.14(2H，m)；2.56(1H，m)；2.20(1H，m)；2.11(2H，m)；2.01(1H，m)；1.84(1H，t，J＝5.7)；1.79(1H，m)；1.74-1.58(3H，m)；1.57-1.39(5H，m)；1.32(1H，d，J＝9.9)；1.24(19H，m)；0.85(9H，m)；0.80(3H，s)。

From (2S)-2-amino-5-[[imino group (nitro amino) methyl] amino]-pentanamide of Embodiment C .1, and N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked borol-2-yls]-the 3-methyl butyl] hydrochloride and suitable carboxylic acid begin, and mainly be listed in and show among the D-1 according to other compounds of above-mentioned experimental procedure preparation.

Table D-1

Follow embodiment D.1 above-mentioned steps and utilize (2S)-2-amino-5-[[imino group (nitro amino) methyl] amino] pentanamide of Embodiment C .1, N-[(1R)-1-[(3aS; 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked borol-2-yls]-the 3-methyl butyl]-hydrochloride and suitable carboxyl are as setting out material, and listed compound among the D-1A is shown in preparation.

Table D-1A

Embodiment D.2

10-(1,3-dioxy-1,3-dihydro-iso-indoles-2-yl)-decyl amide; N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-;

To the 10-that G.1 prepares according to embodiment (1,3-dioxy-1,3-dihydro-isoindole-2-yl)-capric acid (353mg, in anhydrous methylene chloride 1.11mmol) (10ml) solution, add N-methylmorpholine (122 μ l, 1.11mmol).Mixture is cooled to-15 ℃, slowly add again isobutyl chloroformate (144 μ l, 1.11mmol).After 15 minutes, add (2S)-2-amino-5-[[imino group (nitro amino) methyl] amino] pentanamide of Embodiment C .1, and N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked borol-2-yls]-the 3-methyl butyl]-hydrochloride (508mg, 1.01mmol) and another N-methylmorpholine (122 μ l, 1.11mmol).Reaction mixture stirred 4 hours at-15 to 10 ℃, was concentrated into small volume then, and between ETHYLE ACETATE (20ml) and water (10ml), distributed.Water further extracts with ETHYLE ACETATE (10ml).The organic phase that merges is to dried over sodium sulfate and concentrated.Residue absorbs with ETHYLE ACETATE (3ml) and dropwise adds solution to hexane (120ml), stirs under the room temperature simultaneously.Topple over the back and collect solid, and under vacuum dry (730mg, 94%).

¹H?NMR(DMSO-d ₆)：8.81(1H，d，J＝2.7Hz)；8.52(1H，br)；7.98(1H，d，J＝8.05)；7.88(2H，br)；7.85(4H，m)；4.34(1H，m)；4.06(1H，dd，J＝7.1)；3.56(2H，t，J＝7.14)；3.14(2H，m)；2.55(1H，m)；2.19(1H，m)；2.10(2H，t，J＝7.14)；2.0(1H，m)；1.82(1H，t，J＝5.7)；1.78(1H，m)；1.73-1.35(10H，m)；1.31(1H，d，J＝9.9)；1.24(19H，m)；0.84(9H，m)；0.79(3H，s)。

Mainly other compounds according to above-mentioned experimental procedure preparation are listed among the table D-2.

Table D-2

Other compounds according to the method for preparing of embodiment in D.2 are listed among the table D-2A.Embodiment compound D.2.6 is from embodiment 2-amino acetamide D.14, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-amino] carbonyl]-4-[[imino group (nitro amino) methyl]-amino]-butyl], hydrochloride.Embodiment D.2.7 and compound D.2.8 from the 2-of Embodiment C .3 amino acetamide, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 1-methyl butyl]; Hydrochloride.Embodiment 2.9 and 2.10 compound be from (2S)-2-of Embodiment C .3 amino-5-urea groups pentanamide, and N-[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]; Hydrochloride.

Table D-2A

Embodiment D.3

11-cyano group undecanoic amide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl 4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-

Chirality

With PS-carbodiimide (N-carbodicyclo hexylimide-N '-propyl group oxygen ylmethyl PS; 769mg; 1mmol, carrying capacity 1.31mmol/g) and HOAt (1-hydroxyl-7-azepine benzotriazole, 115mg; 0.85mmol) (115mg, methylene dichloride 0.54mmol) (DCM) are (9mL) in the solution to be added to the 11-cyano undecanoic acid.Stir after 10 minutes, add (2S)-2-amino-5-[[imino group (nitro amino) methyl] amino] pentanamide of Embodiment C .1, and N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-, hydrochloride and DIPEA (0.128ml, 0.75mmol).Shaken overnight under the suspension-s room temperature, after filtering the PS-carbodiimide, and with DCM (4 * 6mL) washings for several times.

The VARIAN CHEM ELUT cylinder that organic phase is used through liquid-liquid extraction is with saturated water-based NaHCO ₃Regulate in advance and finally wash with DCM (15mL).Evaporating solvent, and, obtain the required compound of 200mg (yield 61%) with normal phase ISOLUTE SPE-SI post (DCM 9, and MeOH 1) purifying crude reaction thing.

NMR(CDCl ₃)：7.53(s，br，2H)；7.36(d，br，J＝4.7Hz，1H)；6.88(d，J＝8.2Hz，1H)；4.46(m，1H)；4.15(dd，J＝8.5，1.9Hz，1H)；3.19(m，2H)；2.93(m，1H)；2.23(t，J＝7.2Hz，2H)；2.21(m，1H)；2.09(t，J＝7.5，2H)；2.04(m，1H)；1.88(t，J＝5.4Hz，1H)；1.77(m，1H)；1.69(m，1H)；1.64-1.43(m，9H)；1.40-1.26(m，4H)；1.26(s，3H)；1.24-1.12(m，16H)；0.80(d，J＝6.6，3H)；0.79(d，J＝6.6，3H)；0.73(s，3H)。

LC-MS 659.7, MH+.ESI POS; AQA; Atomizer 4kV/ skimmer: 20V/ detector 250C.

Mainly other compounds according to above-mentioned experimental technique preparation are listed among the table D-3.

Table D-3

D.3 other compounds that prepare according to the foregoing description are listed among the table D-3A.

Table D-3A

Embodiment D.4

Naphthalene-2-sulfonamide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-.

Chirality

Under the room temperature, to (2S)-2-of Embodiment C .1 amino-5-[[imino group (nitro amino) methyl]-amino]-pentanamide, N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-, hydrochloride (70mg; 0.14mmol) DCM (4mL) solution in add TEA (0.04mL, 0.31mmol) and naphthalene-2-sulfonic acid chloride (35.1mg, 0.16mmol).After the stirred overnight, (0.04mL, 0.31mmol) (35.1mg 0.16mmol), and lets reaction stirring another night with naphthalene-2-SULPHURYL CHLORIDE to add second section TEA.Then, with saturated K ₂CO ₃The solution washing reaction mixture, and isolating organic phase is concentrated into drying.Reacting coarse product is through the normal phase cylinder of SPE-SI purifying, to obtain title compound (64mg, yield 70%).

NMR(CDCl ₃)：8.42(s，br，1H)；7.96(dd，J＝7.5，2.2Hz，1H)；7.95(d，J＝8.5Hz，1H)；7.89(d，br，J＝7.9Hz，1H)；7.81(dd，J＝8.8，1.9Hz，1H)；7.68-7.57(m，2H)；7.23(s?br，2H)；6.23(s?br，1H)；6.03(d，J＝8.5Hz，1H)；4.19(dd，J＝9.1，2.2Hz，1H)；3.92(s，br，1H)；3.31(m，2H)；2.97(m，1H)；2.26(m，1H)；2.12(m，1H)；1.93(t，J＝5.7Hz，1H)；1.90-1.68(m，6H)；1.30(s，3H)；1.28(m，1H)；1.25(s，3H)；1.06(m，4H)；0.79(s，3H)；0.58(d，J＝9.4Hz，3H)；0.56(d，J＝9.4Hz，3H)。

LC-MS 657.3, MH+, ESI POS; AQA; Atomizer 4kV/ skimmer: 20V/ detector 250C.

Mainly other compounds according to above-mentioned experimental procedure preparation are listed among the table D-4.

Table D-4

Embodiment D.4.9

Naphthalene-2-sulfonamide, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-the 2-hydroxypropyl].

Chirality

With naphthalene-2-sulfonic acid chloride (144mg 0.637mmol) is added to Embodiment C .3 (2S)-amino-(3R)-hydroxyl-butyramide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked borol-2-yls]-the 3-methyl butyl] amino]-carbonyl] hydrochloride and NMM (0.175ml, anhydrous methylene chloride solution 1.59mmol), stirring under 0 ℃ and nitrogen simultaneously.After 6 hours, let mixture heat to room temperature, and stirred overnight.Add 10%NaHCO ₃Solution (10ml), and separating layer.Water further extracts with methylene dichloride (5ml).Organic phase is with 20%NaH ₂PO ₄Solution washing is to dried over sodium sulfate and concentrated.(silica gel, 25g) purifying is with the mixture wash-out of 1: 1 (v/v) hexane and ETHYLE ACETATE through column chromatography for residue.

The product that obtains is white glass appearance solid (219mg, a yield 74%), but still contains some pinine glycols.This product sample (160mg) grinds with the mixture of Anaesthetie Ether (3ml) and hexane (3ml), obtains the pure products (80mg, yield 27%) of white solid.M.p.147-149℃

¹H?NMR(DMSO-d6)：8.40(1H，s)；8.28-8.22(1H，m)；8.11(1H，d，J＝7.7)；8.05(1H，d，J＝8.7)；8.01(1H，d，J＝7.8)；7.81(1H，dd，J＝8.7，1.7)；7.75(1H，s?br.)；7.72-7.61(2H，m)；4.84(1H，s?br.)；4.03(1H，dd，J＝8.5，1.7)；3.82-3.72(2H，m)；2.41-2.33(1H，m)；2.20-2.10(1H，m)；2.02-1.93(1H，m)；1.82-1.72(2H，m)；1.58-1.50(1H，m)；1.36-1.24(1H，m)；1.20(3H，s)；1.18(3H，s)；0.99(3H，d，J＝6.1)；0.94-0.82(2H，m)；0.77(3H，s)；0.63(3H，d，J＝7.1)；0.61(3H，d，J＝7.1)。

Embodiment D.5

(2S)-4-[[imino group (nitro amino) methyl] amino]-2-[(2-naphthyl methyl)-amino]-pentanamide, N-[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl 4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl].

Chirality

With (2S)-2-amino-5-[[imino group (nitro amino) methyl] amino] pentanamide of Embodiment C .1, and N-[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-; (88mg, MeOH 0.175mmol) (4mL) solution is intended to obtain the parent material as free alkali by ISOLUTE PSA cylinder to hydrochloride.Under the room temperature, in the MeOH of free alkali (4mL) solution, add 2-naphtaldehyde (45mg, 0.28mmol) and NaCNBH ₃(18mg, 0.28mmol); Adding AcOH is 4-5 up to the pH of solution.The reaction mixture stirred overnight adds H then ₂O (1mL) concentrates gained solution; Residue is dissolved in AcOEt,, and organic phase is concentrated into drying with brine wash.Dodge chromatography (DCM/MeOH/NH through silica gel ₄OH, 97.5/2.5/0.25) purification reaction crude product obtains required compound (30mg, yield 28%).NMR (CDCl ₃+ D ₂O): 7.81 (m, 3H); 7.71 (s, br, 1H); 7.52-7.38 (m, 3H); 4.66 (s, br, 1H); 4.27 (dd, J=8.8,1.9Hz, 1H); 3.91 with 3.83 (ABq, 2H); 3.39-3.11 (m, 3H); 2.30 (m, 1H); 2.13 (m, 1H); 1.98-1.45 (m, 8H); 1.45 (m, 2H); 1.38 (s, 3H); 1.23 (s, 3H); 1.22 (m, 1H); 0.91 (d, J=6.3Hz, 6H); 0.81 (s, 3H).

LC-MS 607.1, MH+.ESI POS; AQA; Atomizer 4kV/ skimmer: 20V/ detector 250C.

Mainly other compounds according to above-mentioned experimental procedure preparation are listed in table D-5.

Table D-5

Embodiment D.6

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl]] amino] butyl]-N '-(1-naphthyl) urea.

Chirality

Under the room temperature, to (2S)-2-of Embodiment C .1 amino-5-[[imino group (nitro amino) methyl] amino]-pentanamide, N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-, hydrochloride (50mg, CH 0.10mmol) ₃Add in CN (4mL) solution TEA (0.014mL, 0.10mmol) and naphthalene-1-isocyanates (0.014mL, 0.10mmol).Reaction mixture stirred 4 hours, was concentrated into drying then.Residue is dissolved in DCM, with H ₂The O washing; Separate organic layer, and go down to desolventize in vacuum., silica gel obtains the title compound (60mg, yield 94%) of white solid after dodging chromatography (DCM 95, and MeOH 5) purifying.

NMR(CDCl ₃)：8.08(s，br，1H)；7.98(m，1H)；7.79(m，2H)；7.57(d，J＝8.2Hz，1H)；7.51-7.35(m，4H)；7.36(d，J＝7.5Hz，1H)；7.17(s，br，1H)；6.67(d，br，J＝6.6Hz，1H)；4.49(m，1H)；4.20(dd，J＝8.5，1.9Hz，1H)；3.39(m，1H)；3.20(m，1H)；3.04(m，1H)；2.26(m，1H)；2.08(m，2H)；1.93(t，J＝5.6Hz，1H)；1.89-1.55(m，7H)；1.39(m，1H)；1.32(s，3H)；1.31(m，1H)；1.21(s，3H)；1.20(m，1H)；0.85(d，J＝6.0Hz，6H)；0.79(s，3H)。

LC-MS 636.3, MH+.ESI POS; AQA; Atomizer 4kV/ skimmer: 250 ℃ of 20V/ detectors.

Mainly other compounds according to above-mentioned experimental procedure preparation are listed among the table D-6.

Table D-6

Embodiment D.7

Boric acid, [(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(E)-and 3-(naphthalene-2-yl) third-2-alkene acyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-

Chirality

To PS-HOBT (I-hydroxybenzotriazole-6-sulfonamido methylated polystyrene, 277mg, 0.31mmol; Carrying capacity 1.12mmol/g) adds 3-naphthalene-2-base-vinylformic acid (91.2mg in DCM (6mL) and DMF (0.6mL) suspension-s; 0.46mmol), DIC (DIC, 0.22mL; 1.40mmol) and DIPEA (0.05mL, 0.19mmol).Vibration suspension-s 3 hours under the room temperature filters resin then under nitrogen, and with DMF (3 * 5mL), DCM (3 * 5mL), DMF (3 * 5mL) and THF (3 * 5mL) wash several.The resin of thorough drying is suspended among DCM (6mL) and the DMF (0.6mL); And adding Embodiment C .2 [(1R)-1-[[(2S)-and 2-amino-5-[[imino-(nitro amino) methyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-borate hydrochlorate (50mg; 0.14mmol) and DIPEA (0.06mL, 0.20mmol).Reaction mixture shaken overnight under the room temperature.Filter out resin, with DMF (10mL) and DCM (2mL) washing, and concentrated solvent is to dry.Through the normal phase cylinder of ISOLUTE SPE-SI (DCM 1, and MeOH 1) purifying crude compound, obtain title compound (25mg, yield 35%).

NMR(DMSO+D ₂O，343K)：8.06(s，1H)；7.95(d，J＝9.0Hz，1H)；7.94(m，2H)；7.72(d，1H)；7.61(d，J＝14.9Hz，1H)；7.55(d，J＝9.0Hz，1H)；7.55(m，2H)；6.89(d，J＝14.9Hz，1H)；4.40(m，1H)；3.30-3.10(m，3H)；1.82(m，1H)；1.73-1.53(m，4H)；1.50-1.32(m，2H)；0.87(d，J＝6.1Hz，3H)；0.86(d，J＝6.1Hz，3H)。

LC-MS 495.0, [M-18] H+.ESI POS; AQA; Atomizer 5kV/ skimmer: 15V/ detector 250C.

Mainly other compounds according to above-mentioned experimental procedure preparation are listed among the table D-7.

Table D-7

Other compounds according to embodiment above-mentioned steps preparation D.7 are listed among the table D-7A.

Table D-7A

Embodiment D.8

Decyl amide, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-the 2-hydroxypropyl]-

Chirality

Under the room temperature capric acid (220mg, 1.28mmol, 1.2 equivalents) is dissolved in dry DMF (15ml), adds TBTU (410mg, 1.28mmol, 1.2 equivalents), and stirred gained solution 10 minutes.At 0-5 ℃ of following cooling mixture, add NMM (0.35ml, 3.2mmol, 3 equivalents); Add then Embodiment C .3 (2S)-amino-(3R)-hydroxyl-butyramide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl] hydrochloride (430mg, 1.067mmol, 1 equivalent).Solution stirring is poured into after 2 hours in the water (200ml) and with ETHYLE ACETATE (100ml) and extracts.With following solution washing organic layer: Hydrocerol A 2% (20ml), sodium hydrogencarbonate 2% (20ml), NaCl 2% (25ml).Organic solution is filtered and vapourisation under reduced pressure anhydrous sodium sulfate drying, obtains 600mg oil, through silica gel column chromatography (ETHYLE ACETATE/n-hexane 1/1) purifying, obtains the 540mg white solid, and spending the night is suspended in Anaesthetie Ether (5ml) and n-hexane (20ml).Filtering suspension liquid obtains the 110mg white solid.Yield 20%.

Analytical data: m.p.108-110 ℃, TLC silica gel (n-hexane/ethyl acetate 1/1r.f.0.33).Ultimate analysis, calculated value C (66.91%), H (10.26%), N (5.38%), B (2.08%); Measured value C (66.82%), H (10.61%), N (5.35%), B (1.93%).

¹H-NMR(DMSO-d ₆)δ _H：8.81(1H，br)；7.68(1H，d，J＝8.80Hz)；4.93(1H，d，J＝5.2)；4.28(1H，dd，J＝8.8，4.3)；4.05(1H，dd，J＝8.6，1.8)；3.92(1H，m)；2.52(1H，m)；2.20(1H，m)，2.17(2H，t，J＝7.1)；2.00(1H，m)；1.83(1H，t，J＝5.8)；1.78(1H，m)；1.64(1H，m)；1.62(1H，m)；1.49(2H，m)；1.34(1H，d，J＝10.0)；1.31-1.17(21H，m)；1.04(3H，d，J＝6.4)；0.91-0.83(9H，m)；0.81(3H，s)。

Other compounds according to the above-mentioned steps preparation comprise the following example compound:

Embodiment D.8.1

(2S)-2-[(benzyloxycarbonyl) amino]-4-methylpent acid amides, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-the 2-hydroxypropyl]-

Analytical data: TLC (CHCl ₃9/MeOH 1, R.f.0.63), m.p.38-40 ℃, ultimate analysis, calculated value C (64.60%), H (8.54%), N (6.85%); Measured value C (62.44%), H (8.24%), N (7.47%).

¹H?NMR(DMSO-d ₆)δ _H：8.78(1H，br)；7.82(1H，d，J＝8.60Hz)；7.52(1H，d，J＝8.1)；7.40-7.27(6H，m)；5.02(2H，br?s)；5.00(1H，d，J＝5.1)；4.28(1H，dd，J＝8.6，J＝4.2)；4.12(1H，q，J?7.8)；4.05(1H，dd，J＝8.6，J＝1.8)；3.94(1H，m)；2.52(1H，m)；2.19(1H，m)；2.01(1H，m)；1.83(1H，t，J＝5.8)；1.78(1H，m)；1.74-1.55(5H，m)；1.46(2H，m)；1.32(1H，d，J＝10.1)；1.24(3H，s)；1.22(3H，s)；1.04(3H，d，J＝6.2)；0.91-0.82(12H，m)；0.80(3H，s)。

Embodiment D.8.2

10-(1,3-dioxy-1,3-dihydro-iso-indoles-2-the yl)-last of the ten Heavenly stems-acid amides-N-[(1S), (2R)-the 2-hydroxyl, 1-[[(1R)-1-r (3aS; 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino carbonyl]-propyl group]-

Analytical data: TLC (CHCl ₃9/MeOH 1R.f.0.83), ultimate analysis, calculated value C (66.52%), H (8.43%), N (6.37%); Measured value C (66.76%), H (8.48%), N (6.31 ¹H NMR (DMSO-d ₆) δ _H: 8.80 (1H, br); 7.85 (4H, m), 7.67 (1H, d, J=8.80Hz); 4.93 (1H, d, J=5.5), 4.28 (1H, dd, J=8.6,4.0); 4.04 (1H, dd); 3.92 (1H, m); 3.56 (2H, t, J=8.1); 2.49 (1H, m); 2.23-2.12 (3H, m); 2.00 (1H, m); 1.82 (1H, t, J=6.6); 1.78 (1H, m); 1.73-1.53 (5H, m); 1.48 (2H, m); 1.33 (1H, d, J=10.1); 1.31-1.17 (20H, m); 1.03 (3H, d, J=6.2); 0.84 (6H, d, J=6.6); 0.80 (3H, s).

According to the foregoing description D.8, D.8.1 and other compounds of step D.8.2 preparation be listed in table D-8.

Table D-8

Be used for synthetic embodiment D.8.3 according to document step preparation, D.8.7, D.8.11, D.8.12 and midbody carboxylic acid D.8.13.Compound 2, the preparation of 2-dimethyl-capric acid such as Roth etc., J.Med.Chem.1992,35, described in the 1609-1617.Compound 4-(3-pyridyl) phenylformic acid, 3-(3-pyridyl) phenylformic acid and 6-phenyl-2-Pyridinecarboxylic Acid be according to Gong etc., Synlett, 2000, (6), the step preparation described in the 829-831.Compound 3-propoxy benzoic acid is according to Jones, J.Chem.Soc.1943, the step preparation described in the 430-432.

Embodiment D.8.18

The 2-pyrazinecarboxamide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-carbamoyl ethyl]

Chirality

Basically D.8 according to the foregoing description, D.8.1 and step D.8.2, from (2S)-2-amino-3-carbamoyl propionamide of Embodiment C .3; N-[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]; Hydrochloride begins, and prepares this compound.

¹H-NMR(DMSO-d6)：9.20(1H，d，J＝1.29Hz)；9.02(1H，d，J＝8.52Hz)；8.91(1H，d，J＝2.45Hz)；8.81-8.76(2H，m)；7.42(1H，s)；6.95(1H，s)；5.00-4.80(1H，m)；4.30-4.08(1H，m)；2.85-2.72(1H，m)；2.62-2.56(2H，m)；2.25-2.15(1H，m)；2.06-1.98(1H，m)；1.84(1H，t，J＝5.54Hz)；1.81-1.76(1H，m)；1.72-1.58(2H，m)；1.32-1.26(1H，m)；1.23(8H，d，J＝5.36Hz)；0.85-0.79(9H，m)。

Embodiment D.8.19

Decyl amide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-carbamoyl ethyl]

Chirality

Embodiment D.8.20

The 4-butyl benzamide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl 4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-carbamyl ethyl]

Chirality

Basically D.8 according to the foregoing description, D.8.1 and step D.8.2, from (2S)-2-amino-3-carbamoyl propionamide of Embodiment C .3; N-[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]; This compound of hydrochloride preparation.

Embodiment D.9

Decyl amide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl 4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-[(4-toluyl) amino] ethyl]-

Capric acid (330mg, 1.95mmol, 1.2 equivalents) is dissolved in the dry DMF (20ml), and under nitrogen and room temperature, adds TBTU (620mg, 1.95mmol, 1.2 equivalents).Solution stirred 10 minutes, 0-5 ℃ of cooling, added (2S)-2-amino-3-[(4-methyl benzoyl) amino] propionamide of NMM (0.53ml, 4.9mmol, 3 equivalents) and Embodiment C .4; N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-; Hydrochloride (800mg, 1.58mmol, 1 equivalent) stirred 3 hours under the gained mixture room temperature.Solution is poured into water (200ml), with ETHYLE ACETATE (100ml) extraction, uses Hydrocerol A 2% (50ml) again, sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml) solution washing.Organic solution is filtered anhydrous sodium sulfate drying, evaporation, and be suspended in Anaesthetie Ether (20ml) 30 minutes.This suspension filtered obtains the 330mg white solid after the drying.Yield 33%.M.P.:134-136 ℃, TLC, silica gel, (eluent n-hexane/ethyl acetate, r.f.0.5).Ultimate analysis, calculated value C (69.33%), H (9.37%), N (6.74%), B (1.73%); Measured value C (%), H (%), N (23%), B (%).

¹H?NMR(DMSO-d ₆)8.74(1H，d，J＝3.5Hz)；8.25(1H，t，J＝5.6)；7.95(1H，d，J＝7.9)；7.71(2H，d，J＝8.1)；7.25(2H，t，J＝8.1)；4.59(1H，m)；4.1(1H，dd，J＝1.8，8.8)；3.49(2H，m)；2.59(1H，m)；2.35(3H，s)；2.20(1H，m)；2.09(1H，t，J＝7.3)；2.02(1H，m)；1.83(1H，t，J＝5.5)；1.78(1H，m)；1.62(2H，m)；1.44(2H，m)；1.36-1.21(17H，m)；1.25(3H，s)，1.22(3H，s)；0.85(3H，t，J＝6.8)；0.80(9H，m)。

Embodiment D.10

2-S-capryl amino-3-(caproyl is amino)-propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl].

Capric acid (170mg, 0.98mmol, 1.2 equivalents) is dissolved in the dry DMF (15ml), and under nitrogen and room temperature, adds TBTU (310mg, 0.98mmol, 1.2 equivalents).Solution stirred 20 minutes, 0-5 ℃ of cooling, and 2-S-amino-3-of adding NMM (0.271ml, 2.46mmol, 2.5 equivalents) and Embodiment C .5 (caproyl is amino)-propionamide; N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]; Hydrochloride (400mg, 0.82mmol, 1 equivalent) stirred 3 hours under the gained mixture room temperature.Solution is poured into water (150ml), with ETHYLE ACETATE (100ml) extraction, and with Hydrocerol A 2% (50ml), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml) solution washing.Organic solution is to anhydrous sodium sulfate drying, filters, and evaporates and is suspended in ETHYLE ACETATE (20ml) 30 minutes.Suspension filtered and drying obtain the 230mg white solid, yield 47%.

Analytical data: m.p.135-137 ℃, and TLC silica gel (eluent hexane/ethyl acetate 2/1, R.f.=0.27).Ultimate analysis, calculated value C (67.64%), H (10.35%), N (6.96%); Measured value C (66.93%), H (10.29%), N (7.14%).

¹H?NMR(DMSO-d ₆)δ _H：8.67(1H，d，J＝2.9Hz)；7.83(1H，d，J＝8.2)；7.67(1H，t，J＝5.5)；4.41(1H，m)；4.10(1H，dd，J＝1.5，8.6)；3.25(2H，m)；2.56(1H，m)；2.20(1H，m)；2.13-1.95(5H，m)；1.84(1H，t，J＝5.5)；1.78(1H，m)；1.64(2H，m)；1.46(4H，m)；1.35-1.15(27H，m)；0.84(9H，m)；0.79(3H，s)。

Embodiment D.11

2-S-capryl amino-3-(4-fluorine sulfonamido) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl].

Capric acid (160mg, 0.94mmol, 1.2 equivalents) is dissolved in the dry DMF (20ml), and under room temperature and nitrogen, adds TBTU (300mg, 0.94mmol, 1.2 equivalents).Solution stirred 20 minutes, 0-5 ℃ of cooling down, and 2-S-amino-3-(4-fluorine sulfonamido) propionamide of adding NMM (0.259ml, 2.36mmol, 2.5 equivalents) and Embodiment C .6; N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]; Hydrochloride (430mg, 0.78mmol, 1 equivalent) stirred 2 hours under the gained mixture room temperature.Solution is poured in the water (200ml), with ETHYLE ACETATE (100ml) extraction, uses following solution washing: Hydrocerol A 2% (50ml), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml).Organic solution is filtered anhydrous sodium sulfate drying, evaporation, and through silica gel column chromatography (eluent n-hexane/ethyl acetate 2/1) purifying.Solvent evaporation adds the n-hexane, obtains the 100mg solid.Yield 19%.

Analytical data: m.p.83-85 ℃, and TLC silica gel (eluent hexane/ethyl acetate 2/1, R.f.=0.53).

¹H?NMR(DMSO-d ₆)δ _H：8.45(1H，d，J＝3.8Hz)；7.83(3H，m)；7.63(1H，t，J＝6.2)；7.42(2H，t，J＝8.8)；4.40(1H，m)；4.12(1H，dd，J＝1.5，8.6)；2.95(2H，m)；2.64(1H，m)；2.21(1H，m)；2.17(2H，t，J＝7.3)；2.01(1H，m)；1.83(1H，t，J＝5.5)；1.78(1H，m)；1.62(2H，m)；1.45(2H，m)；1.4-1.1(23H，m)；0.87-0.8(9H，m)；0.79(3H，s)。

Embodiment D.12

2-S-caprinoyl amino-3-(3,4-Dimethoxyphenyl acetylamino) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl].

Capric acid (80mg, 0.48mmol, 1.2 equivalents) is dissolved in dry DMF (20ml), under room temperature and nitrogen, adds TBTU (150mg, 0.48mmol, 1.2 equivalents).Solution stirred 20 minutes, 0-5 ℃ of cooling, and 2-S-amino-3-(3 of adding NMM (0.13ml, 1.2mmol, 2.5 equivalents) and Embodiment C .7; 4-Dimethoxyphenyl acetylamino) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]; Hydrochloride (230mg, 0.4mmol, 1 equivalent) stirred 2 hours under the gained mixture room temperature.Solution is poured into water (200ml), with ETHYLE ACETATE (100ml) extraction, uses following solution washing: Hydrocerol A 2% (50ml), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml).Organic solution is filtered anhydrous sodium sulfate drying, evaporation, and through silica gel column chromatography (eluent n-hexane/ethyl acetate 1/1) purifying.Obtain 100mg hyaloid solid after the solvent evaporation.Yield 35.7%.

Analytical data: TLC silica gel (eluent hexane/ethyl acetate 1/1, R.f.=0.53).Ultimate analysis, calculated value C (67.13%), H (9.25%), N (6.02%); Measured value C (65.38%), H (9.20%), N (5.49).

¹H?NMR(DMSO-d ₆)δ _H：8.65(1H，d，J＝3.5Hz)；7.84(2H，m)；6.83(2H，m)；6.72(1H，dd，J＝1.7，8.1)；4.43(1H，m)；4.10(1H，dd，J＝1.8，8.6)；3.72(3H，s)；3.70(3H，s)；3.30(2H，s)；3.27(2H，m)；2.58(1H，m)；2.19(1H，m)；2.02(3H，m)；1.84(1H，t，J＝5.5)；1.78(1H，m)；1.63(2H，m)；1.43(2H，m)；1.35-1.15(23H，m)；0.87-0.8(9H，m)；0.79(3H，s)。

Embodiment D.13

2-S-capryl amino-3-(phenyl urea groups) propionamide, N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl].

Capric acid (170mg, 0.99mmol, 1.2 equivalents) is dissolved in dry DMF (20ml), and under room temperature and nitrogen, adds TBTU (310mg, 0.99mmol, 1.2 equivalents).Solution stirred 20 minutes, 0-5 ℃ of cooling down, 2-S-amino-3-(phenyl urea groups) propionamide of adding NMM (0.27ml, 2.4mmol, 2.5 equivalents) and Embodiment C .8; N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]; Hydrochloride (420mg, 0.82mmol, 1 equivalent) and gained mixture stirred 2 hours at 0 ℃.Solution is poured into water (200ml), with ETHYLE ACETATE (100ml) extraction, uses following solution washing: Hydrocerol A 2% (50ml), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml).Organic solution is to anhydrous sodium sulfate drying, filters, and evaporates and is suspended in Anaesthetie Ether (20ml) 1 hour, filters also dryly under vacuum, obtains the 140mg white solid, through silica gel column chromatography (n-hexane/ethyl acetate 1/1) purifying.Yield 25%.

Analytical data: TLC silica gel (eluent hexane/ethyl acetate 1/1, R.f.=0.4).

¹H?NMR(DMSO-d ₆)δ _H：8.73(1H，d，J＝3.1Hz)；8.64(1H，br?s)；7.97(1H，d，J＝8.2)；7.36(2H，d，J＝8.1)；7.19(2H，t，J＝8.1)；6.87(1H，t，J＝8.1)；6.1(1H，t，J＝6.0)；4.44(1H，m)；4.10(1H，dd，J＝1.8，8.6)；3.41(1H，m)；3.22(1H，m)；2.59(1H，m)；2.19(1H，m)；2.10(2H，t，J＝7.3)；2.02(1H，m)；1.84(1H，t，J＝5.5)；1.78(1H，m)；1.64(2H，m)；1.46(2H，m)；1.35-1.15(23H，m)；0.87-0.8(9H，m)；0.79(3H，s)。

Embodiment D.14

The 2-amino acetamide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl 4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl], hydrochloride

Chirality

To the N-Boc-glycocoll (383mg, anhydrous methylene chloride 2.18mmol) (20ml) solution, add N-methylmorpholine (275 μ l, 2.5mmol).Mixture is cooled to-15 ℃, slowly add then isobutyl chlorocarbonate (286 μ l, 1.2mmol).After 15 minutes, add (2S)-2-amino-5-[[imino group (nitro amino) methyl] amino] pentanamide of Embodiment C .1, and N-[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked borol-2-yls]-the 3-methyl butyl]-hydrochloride (1.00g, 2.0mmol) and other add N-methylmorpholine (275 μ l, 2.5mmol).Reaction mixture stirred 4 hours at-15 ℃-10 ℃, was concentrated into small volume then, and between ETHYLE ACETATE (100ml) and water (50ml), distributed.Water further extracts with ETHYLE ACETATE (20ml).The organic phase that merges is to dried over sodium sulfate and concentrated.Residue absorbs with ETHYLE ACETATE (5ml), and solution dropwise is added in the hexane (120ml), stirs under the room temperature simultaneously.Decant is collected solid and drying (1.18g, 95%) under vacuum.(1.08g 1.73mmol) is dissolved among the THF (15ml) midbody of this Boc-protection of part, adds 4NHCl De dioxane solution then.Stir under the room temperature after 5 hours, mixture concentrates, and residue grinds with Anaesthetie Ether (50ml).The gained white solid washs with Anaesthetie Ether through filtering collection, and dry under vacuum, generates the title compound (yield 88%) of 856mg.

¹H?NMR(DMSO-d ₆)：8.76(1H，d，J＝3.1Hz)；8.68(1H，d，J＝8.1)；8.56(1H，br)；8.06(3H，m)；7.91(2H，br)；4.43(1H，m)；4.14(1H，dd，J＝8.6，J＝1.6)；3.60(2H，m)；3.15(2H，br)；2.67(1H，m)；2.23(1H，m)；2.04(1H，m)；1.87(1H，t，J＝5.8)；1.81(1H，m)；1.75-1.60(3H，m)；1.52(3H，m)；1.41-1.28(3H，m)；1.27(3H，s)；1.23(3H，s)；0.86(3H，d，J＝6.4)；0.84(3H，d，J＝6.4)；0.81(3H，s)。

Embodiment D.15

The amino propionamide of 3-, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]; Hydrochloride

Chirality

CIH

To at the embodiment of 0 ℃ of cooling 3-[[(1,1-dimethyl ethyoxyl) carbonyl] amino] propionamide D.3.118, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl-] amino] butyl]-; (42mg, Anaesthetie Ether 0.075mmol) (1.0ml) solution, Anaesthetie Ether (2ml) solution of adding 10%v/v hydrochloride.Mixture stirred 5 hours, heated to room temperature simultaneously.The gained solid by filtration is collected, and (3 * 3ml) wash, and dry under vacuum, obtain 33mg title compound (yield 76%) with Anaesthetie Ether.

LC-MS 538.7, MH+.ESI POS; AQA; Atomizer 4kV/ skimmer: 20V/ detector 250C.

According to the foregoing description, other compounds that the compound of corresponding Boc protection begins to prepare from show D.3 are listed in following table D-15.

Table D-15

Embodiment D.16

Synthesizing of other compounds

Follow embodiment step D.9-D.13, through the midbody prepared in reaction following compounds of capric acid and Embodiment C .9.

Embodiment D.17

The 4-butyl benzamide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-(amino-ethyl)-hydrochloride.

With embodiment 4-butyl benzamide D.16.6, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-[(benzyloxycarbonyl acid amides) ethyl]-(400mg; 0.62mmol, 1 equivalent) and be dissolved in 1,4-dioxanes (10ml) and methyl alcohol (5ml).Add Pd/C 10% (40mg) and HCl4N 1,4-diox (1.1 equivalent) to this solution.Mixture is hydrogenation under 1 bar pressure.When reaction finishes, celite is filtered Pd/C, decompression goes down to desolventize, and obtains white foam.Yield 95%, 320mg.Analytical data:

¹H?NMR(DMSO-d6)：8.76(1H，d)；8.55(1H，d)；8.15(3H，brs)；7.95(2H，d)；7.25(2H，d)；4.8(1H，m)；4.2(1H，d)；2.80(1H，m)；2.62(2H，t)；2.23(1H，m)；2.04(1H，m)；1.87(1H，t)；1.80(1H，m)；1.75-1.50(2H，m)，(2H，m)；1.41-1.20(6H，d)，(6H，m)；1.0-0.80(3H，d)；(3H，d)；(3H，s)，(3H?t)。

Embodiment D.18

2-S-(4-butyl benzene formamido group)-3-(2-pyrazine and carbonylamino)-N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl].

2-pyrazine carboxylic acid (76mg, 0.61mmol, 1.1 equivalents) is dissolved in dry DMF (5ml), and under room temperature and nitrogen, adds TBTU (200mg, 0.61mmol, 1.1 equivalents).Solution stirred 15 minutes, 0-5 ℃ of cooling, added NMM (0.20ml, 1.85mmol, 3.3 equivalents) and embodiment 4-butyl benzamide D.17; N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-(amino-ethyl)-hydrochloride; (310mg, 0.56mmol, 1 equivalent), the gained mixture stirred 4 hours at 25 ℃.Solution is poured into water (100ml), with ETHYLE ACETATE (50ml) extraction, uses following solution washing: Hydrocerol A 2% (50ml), NaCl 2% (50ml), sodium hydrogencarbonate 2% (50ml), NaCl 2% (50ml).Organic solution is to anhydrous sodium sulfate drying, filters, and evaporation, and be suspended in Anaesthetie Ether-n-hexane 1 hour obtains white solid, filter and vacuum under obtain white powder after the drying.Yield 52%.180mg。

Analytical data: M.p.70-72 ℃.

¹H?NMR(DMSO-d6)：9.20(1H，s)；9.0(1H，t)；8.85(1H，d)；8.8(1H，d)；8.78(1H，d)；8.60(1H，d)；7.82(2H，d)；7.35(2H，d)；4.8(1H，m)；4.1(1H，d)；3.80(1H，m)；3.62(1H，m)；2.82(1H，b)；2.65(2H，m)；2.2-2.0(2H，m)；1.80(1H，m)；1.75-1.50(2H，m)，(2H，m)；1.41-1.20(6H，d)，(6H，m)；1.0-0.80(3H，d)；(3H，d)；(3H，s)，(3H?t)。

Embodiment D.19

The 4-butyl benzamide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-[4-fluoro-benzsulfamide] ethyl]-

Under 0-5 ℃, embodiment 4-butyl benzamide D.17, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-[(benzyloxycarbonyl acid amides) ethyl]-, (2; 75g, 5,02mmol, 1 equivalent) be dissolved in anhydrous methylene chloride.Dropwise add N-methylmorpholine (NMM) (1,11g, 11,04mmol, 2,2 equivalents) after in this solution, adding 4-fluorobenzene SULPHURYL CHLORIDE (1,07g, 5,52mmol, 1,1 equivalent) and several minutes.Mixture stirred 30 minutes at 0-5 ℃, stirred 1 hour at 10 ℃ then.Decompression goes down to desolventize, and crude product is dissolved in ETHYLE ACETATE, and with Hydrocerol A 2% (50ml) solution, again with sodium hydrogencarbonate 2% (50ml) solution and sodium-chlor 2% (50ml) solution washing.Solution is to anhydrous sodium sulfate drying, and decompression is evaporating solvent down.Crude product is through silica gel column chromatography (eluent ETHYLE ACETATE/n-hexane 1/2) purifying, and the level of collection is divided decompression evaporation down, and white solid is suspended in Anaesthetie Ether, filters and vacuum-drying, obtains white wax.Yield 60%, 2g.Analytical data:

¹H?NMR(DMSO-d6)：8.60(1H，d)；8.30(1H，d)；7.85(3H，m)；7.8(2H，d)；7.38(2H，d)；7.30(2H，d)；4.62(1H，m)；4.15(1H，d)；3.25(2H，br)；2.61(3H，m)；2.3-2.0(1H，m)；(1H，m)；1.80(1H，m)；1.75-1.50(2H，m)，(2H，m)；1.41-1.20(6H，d)，(6H，m)；1.0-0.80(3H，d)；(3H，d)；(3H，s)，(3H?t)。

Embodiment D.20

The 4-butyl benzamide, N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two evil borol-2-bases-]-the 3-methyl butyl] amino] carbonyl]-2-[(2,5-dimethyl-2H-pyrazoles) carbonylamino] ethyl]-

Embodiment 4-butyl benzamide D.17, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-[(benzyloxycarbonyl acid amides) ethyl]-, (0,9g; 1,64mmol, 1 equivalent) be dissolved in anhydrous methylene chloride (10ml).Gained solution is cooled to 0 ℃＜T＜5 ℃, and adds N-methyl-morpholine (0.381g, 3.78mmol, 2.3 equivalents).In mixture, add 1,3-dimethyl--1H-pyrazoles-5-carbonyl chloride (Rn [55458-67-8]) (0.286mg, 1,8mmol, 1,1 equivalent).Mixture stirred 1 hour, and temperature is increased to 20 ℃.Mixture decompression evaporation down is suspended in ETHYLE ACETATE (50ml), with 2% citric acid solution (30ml), and 2% sodium hydrogencarbonate (30ml), 2% sodium-chlor (30ml) washing.Organic layer is to anhydrous sodium sulfate drying, and vapourisation under reduced pressure.Crude product is through silica gel column chromatography (eluent ETHYLE ACETATE/n-hexane 8/2) purifying.Obtain white powder after the cut evaporation of collecting, be suspended in Anaesthetie Ether, obtain required compound after the filtration.Yield 65%, 650mg.Rf.0.62。Analytical data: M.p.62-64 ℃.

¹H?NMR(DMSO-d6)：8.82(1H，d)；8.40(2H，m)；7.85(2H，d)；7.3(2H，d)；6.5(1H，s)；4.8(1H，m)；4.15(1H，d)；3.9(3H，s)；3.61(2H，m)；2.65(3H，m)；2.25(1H，m)；2.15(3H，s)；2.0(1H，m)；1.80(1H，m)；1.75-1.50(4H，m)，1.41-1.20(5H，m)，(6H，m)；0.90(3H，t)；0.8(9H，m)；

Embodiment D.21

The 4-butyl benzamide, N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two evil borol-2-bases-]-the 3-methyl butyl] amino] carbonyl]-2-(4-aminomethyl phenyl urea groups sulfonamido) ethyl]-

Embodiment 4-butyl benzamide D.17, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-[(benzyloxycarbonyl acid amides) ethyl]-, (0,7g; 1,27mmol, 1 equivalent) be dissolved among the anhydrous THF (10ml), solution is 0-5 ℃ of cooling.Add triethylamine (0,4ml, 1,8mmol, 2,2 equivalents) and embodiment (4-aminomethyl phenyl)-urea groups-SULPHURYL CHLORIDE (0,34g, 1,38mmol, 1,09 equivalent) G.1X.Suspension-s is poured into Hydrocerol A 1% solution (30ml) then, and extracts with ETHYLE ACETATE (50ml) in 25 ℃ of stirring 1 hour.Organic solution, is filtered anhydrous sodium sulfate drying with sodium-chlor 2% solution washing, and decompression evaporation down obtains crude product, through silica gel column chromatography (eluent ETHYLE ACETATE/n-hexane 1/1) purifying Rf 0.64.The level of collecting is divided evaporation, and oil and Anaesthetie Ether coevaporation are to obtain white foam.Yield 31%, 280mg.

Analytical data: M.p.115-120 ℃.

¹H?NMR(DMSO-d6)：8.80(1H，s)；8.40(1H，d)；7.82(2H，d)；7.3(2H，d)；7.25(2H，d)；7.00(2H，d)；4.62(1H，m)；4.15(1H，d)；2.61(3H，m)；2.3-2.0(3H，s)；1.80(1H，m)；1.75(2H，m)，1.6(4H，m)，1.2(13H，m)；0.9(3H，s)，0.8(9H?m)。

Embodiment D.22

The 4-phenoxy benzamide, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl 4,6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-(3-phenyl-urea groups) ethyl]-

Chirality

With embodiment 4-phenoxy benzamide D.25.2, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1; 3,2-benzo two is disliked the borol-2-yls]-the 3-methyl butyl] amino] carbonyl]-2-(amino) ethyl]-hydrochloride (1g, 17mmol, 1 equivalent) is dissolved in anhydrous methylene chloride (30ml); And adding N-methyl-morpholine (0.2g, 18.8mmol, 1.1 equivalents).The solution cooling is at 0-5 ℃, and the methylene dichloride (ml) of adding phenyl isocyanate (0.22g, 17.7mmol, 1.1 equivalents).Mixture stirred 1 hour down at 0-5 ℃.Solution washs with sodium-chlor 2% solution (50ml), to anhydrous sodium sulfate drying, and vaporising under vacuum.Crude product is suspended in Anaesthetie Ether (20ml), stirs 2 hours, filters, and 50 ℃ of following vacuum-dryings, obtains white powder.Yield 74.3%, 0.84g.

Analytical data: M.p.143-145 ℃.

¹H?NMR(DMSO-d6)：8.9(1H，d)；8.75(1H，s)；8.59(1H，d)；7.95(2H，d)；7.45(2H，t)；7.35(2H，d)；7.2(3H，m)；7.1(4H，m)；6.9(1H，m)；6.25(1H，t)；4.65(1H，m)；4.10(1H，d)；3.65(1H，m)；3.4(1H，m)；2.6(1H，m)；2.2(1H，m)；2.1(1H，m)；1.85(2H，m)；1.65(2H，m)，1.3(3H，m)；(6H，d)；0.80(9H，t)。

Embodiment D.23

The 4-butyl benzamide, N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethyl-4,6-methylene-1,3,2-benzo two evil borol-2-bases-]-the 3-methyl butyl] amino] carbonyl]-2-(4-Methyl benzenesulfonyl urea groups) ethyl]-

With embodiment 4-butyl benzamide D.17, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-(amino-ethyl)-hydrochloride (560mg; 1.07mmol, 1 equivalent) and be dissolved in anhydrous methylene chloride (20ml), solution cools off at 0-5 ℃.Add N-methyl-morpholine (0.125ml, 1.129mmol, 1.1 equivalents); With 4-tolylsulfonyl isocyanic ester (0.22g, 1.12mmol, 1.1 equivalents), stirred 2 hours under the mixture room temperature.Mixture is with Hydrocerol A 2% solution (20ml) and sodium-chlor 2% solution (25ml) washing.Organic layer filters anhydrous sodium sulfate drying, and vapourisation under reduced pressure.Crude product is dissolved in Anaesthetie Ether (40ml), and evaporating solvent.Crude product is suspended in n-hexane (20ml), stirs 1 hour under the room temperature, filter, and dry under 50 ℃ of following vacuum, thus white powder obtained.Yield 75.6%, 0.55g.

Analytical data: M.p.168-170 ℃.

¹H?NMR(DMSO-d6)：10.8(1H，s)；8.75(1H，d)；8.35(1H，d)；7.75(4H，m)；7.35(5H，m)；6.65(1H，t)；4.5(1H，t)；4.1(1H，d)；3.5(1H，m)；3.25(1H，m)；2.65(3H，m)；2.3(3H，d)；2.2(1H，m)；2.1(1H，m)；1.80(2H，m)；1.65(4H，m)，1.3(12H，m)；0.80(12H，m)。

Embodiment D.24

Synthesizing of other compounds

Follow embodiment step D.18-D.23, with embodiment D.17 or midbody D.25 and appropriate commercially available carboxylic acid the preparation method of following compounds is, carboxylic acid halides; Sulfonic acid halide, isocyanic ester, sulfonyl isocyanate; Or with embodiment G.14, G.15 and compound G.16 reaction.All compounds that obtain are characterised in that ¹H-NMR.

Table D-24

Embodiment D.25

Synthesizing of other compounds

Follow the step of embodiment D17, from embodiment D.16.8 and compound D.16.9 begin, the preparation following compounds.

Table D-25

Embodiment D.26

The 4-butyl benzamide, N-[(1R)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-[(4-methyl benzoyl) amino] ethyl]-

Chirality

Follow and be used to prepare the D.17 same step of compound of embodiment, utilize the D-asparagine, preparation intermediate 4-butyl benzamide as parent material; N-[(1R)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-2-(amino-ethyl)-hydrochloride.Then, follow embodiment D.18 described in step, this midbody and 4-methyl benzoic acid obtain title compound.

¹H?NMR(MeOD-d4)：8.88(2H，d)；8.45(2H，m)；7.8(2H，d)；7.7(2H，d)；7.35(2H，m)；7.25(2H，d)；4.75(1H，m)；4.1(1H，d)；3.8(1H，m)；3.65(2H，m)；2.65(3H，m)；2.2(1H，m)；2.1(1H，m)；1.8(2H，m)；1.6(4H，m)；1.3-1.1(2H，m)；0.9-0.80(14H，m)。

Embodiment E .1

Boric acid, [(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-naphthoyl base) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-.

Chirality

Embodiment naphthalene-2-formamide D.1.1, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl]-amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-(564mg; 0.90mmol), 2-methyl-propyl boric acid (222mg, 2.19mmol) with the mixture of 4N hydrochloride dioxanes solution (225 μ l) at methyl alcohol: stirring 4 hours under the room temperature in hexane (40: 60) multiphase mixture (10ml).Add hexane (4ml), mixture stirs a little while, shifts out hexane layer then.(100mg 0.99mmol), and at room temperature stirred the mixture 3 hours to add fresh hexane (5ml) and 2-methyl-propyl boric acid.Shift out hexane layer, and with hexane (2 * 5ml) washing methyl alcohol phases.The residue that methyl alcohol obtains after concentrating mutually is through the silica gel column chromatography purifying, at first with eluent ethyl acetate, then with 40: 40: 20 acetone: methyl alcohol: hexanes mixtures wash-out.Product heavily is dissolved in the mixture of ETHYLE ACETATE (250ml) and methyl alcohol (6ml), and (2 * 25ml) washing organic phases are to dried over sodium sulfate and concentrated with water.Residue under 80 ℃ of vacuum dry 3 hours obtains the product (280mg, yield 64%) of white solid.M.p.170-190℃。

¹H?NMR(DMSO-d ₆)：8.76(1H，m)；8.51(2H，br)；8.09-7.09(5H，m)；7.88(2H，br)；7.60(2H，br)；4.67(1H，m)；3.17(2H，m)；2.58(1H，m)；1.81(2H，m)；1.56(3H，m)；1.38-1.11(4H，m)；0.83(1H，m)；0.81(1H，m)；0.74(3H，d，J＝6.4)；0.74(3H，d，J＝6.4)。

Ultimate analysis calculated value: C 54.33% H6.43% N 17.28% B2.22%

Measured value: C 54.87% H6.64% N 17.00% B2.12%

Mainly other compounds according to above-mentioned experimental procedure preparation are listed in table E-1.

Table E-1

Other compounds according to the foregoing description step preparation E.1 are listed among the table E-1A.

Table E-1A

Other compounds according to the foregoing description step preparation E.1 are listed among the table E-1B.

Table E-1B

According to the foregoing description step E.1, from embodiment D.8.19 and other compounds that begin to prepare of compound D.8.20 be listed in table E-1C.

Table E-1C

According to the foregoing description step E.1, from embodiment D.2.9 and other compounds that begin to prepare of compound D.2.10 be listed in the table E-1D.

Table E-1D

Embodiment E .2

Boric acid, [(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(decanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-.

Chirality

With embodiment decyl amide D.1, N-[(1S)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5; 5-trimethyl-4,6-methylene-1,3; 2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-(77mg 0.12mmol) is dissolved in Et ₂O (1mL), 0 ℃ of careful down HCl 37% (2mL) that adds.Let reaction mixture heat to room temperature, and shaken overnight.Mixture is concentrated into drying, and residue is dissolved in MeOH (1mL), through ISOLUTE PSA cylinder, and washs with MeOH.Solvent evaporation, reacting coarse product obtain title compound (19mg, yield 33%) with ISOLUTE SPE-DIOL cylinder (DCM: MeOH 1: 1) purifying.

NMR(DMSO+D ₂O，343K)：4.20(m，1H)；3.13(m，2H)；3.05(m，1H)；2.10(t，J＝6.2Hz，2H)；1.69(m，1H)；1.53-1.40(m，4H)；1.39-1.20(m，14H)；0.84(m，9H)。

LC-MS 468.9, MH+.ESI POS; AQA; Atomizer 4kV/ skimmer: 250 ℃ of 20V/ detectors.

Mainly turn to and be listed among the table E-2 according to other of above-mentioned experimental procedure preparation.

Table E-2

Other compounds according to the foregoing description step preparation E.2 are listed in table E-2A.

Table E-2A

Embodiment E .3

Boric acid, [(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(4-butylbenzene-formyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl].

Chirality

With embodiment 4-butyl benzamide D.3.179, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino]-carbonyl]-the 2-hydroxypropyl]-(1.38g; 2.63mmol), (0.75g, 7.37mmol) mixture with 2N aqueous hydrochloric acid solution (2ml) stirred 16 hours under the room temperature in methyl alcohol (20ml) and hexane (20ml) multiphase mixture 2-methyl-propyl boric acid.Mixture shifts out hexane layer then with methyl alcohol (20ml) and hexane (20ml) dilution.Add ETHYLE ACETATE (50ml) to methanol layer, then concentrate.Residue is with up in ethyl acetate, and enriched mixture.Repeat this step (2-3 time), up to obtaining amorphous white solid.Then, solid grinds with Anaesthetie Ether (10-15ml), and decant shifts out supernatant.Repeat this step 4 time.After further grinding with Anaesthetie Ether (15ml), white solid is collected through filtering, and under vacuum drying at room temperature (0.724g, yield 70%).

¹H?NMR(MeOH-d4)：7.83(2H，d，J＝8.2)；7.34(2H，d，J＝8.2)；4.77(1H，d，J＝6.4)；4.36-4.28(1H，m)；2.77(1H，t，J＝7.6)；2.71(2H，t，J＝7.6)；1.72-1.58(3H，m)；1.46-1.32(4H，m)；1.29(3H，d，J＝6.4)；0.97(3H，t，J＝7.34)；0.94(6H，dd，J＝1.1，6.6)

Other compounds according to the foregoing description step preparation E.3 are listed among the table E-3.

Table E-3

Embodiment E .4

Boric acid, [(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[[4-(3-pyridyl) benzoyl] amino]-1-oxo butyl] amino]-the 3-methylbutyl].

Chirality

With embodiment 4-(pyridin-3-yl) benzamide D.8.3, N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S; 6S, 7aR)-six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]-the 2-hydroxypropyl]-(155mg; 0.283mmol), (81mg, 0.793mmol) mixture with 2N aqueous hydrochloric acid solution (0.3ml) stirred 24 hours under the room temperature in the multiphase mixture of methyl alcohol (3ml) and hexane (3ml) 2-methyl-propyl boric acid.Shift out hexane layer, methanol layer washs with fresh hexane (about 5ml).(10ml) is added to methanol layer with ETHYLE ACETATE, then concentrates.Residue is with up in ethyl acetate, then enriched mixture.Repeat this step (2-3 time), up to obtaining amorphous white solid.Then, solid grinds with Anaesthetie Ether (5ml), and decant shifts out supernatant.Repeat this step.Residue (126mg) merges with the product (140mg) of similar preparation, and is dissolved in ETHYLE ACETATE (about 40ml) and small amount of methanol (2-3ml).Solution is with NaCl saturated solution (7ml) and 10%NaHCO ₃Mixture washing (2ml).Separating layer, and with ETHYLE ACETATE (2 * 20ml) further wash water.The organic phase that merges is to dried over sodium sulfate and concentrated.Residue absorbs with ETHYLE ACETATE (about 20ml) and minimum methyl alcohol, is concentrated into small volume (about 5ml) then.Collect the gained white solid through filtering, and in 50 ℃ of following vacuum-dryings (160mg, total recovery 65%).

¹H?NMR(MeOH-d4)：8.90(1H，s)；8.49(1H，d，J＝4.0)；8.20(1H，d，J＝8.1)；8.06(2H，d，J＝8.1)；7.85(2H，d，J＝8.1)；7.58(1H，t?br.，J＝6.0)；4.80(1H，d，J＝3.9)；4.40-4.29(1H，m)；2.78(1H，t，J＝7.5)；1.73-1.61(1H，m)；1.38(2H，t，J＝6.9)；1.31(3H，d，J＝6.3)；0.94(6H，d，J＝6.31)。

Other compounds according to the foregoing description step preparation E.4 are listed in table E-4.

Table E-4

Embodiment E .5

Boric acid, [(1R)-1-[[(2S)-and 3-(2-pyrazine carbonylamino)-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]

With D.18 2-S-(4-butyl benzene formamido group)-3-(2-pyrazinyl carbonylamino)-N-of embodiment [(1S)-1-[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethyl-4; 6-methylene-1,3,2-benzo two is disliked the borol-2-yl]-the 3-methyl butyl] amino] carbonyl]; (120mg, 0.19mmol, 1 equivalent) is dissolved in methyl alcohol (2ml) and n-hexane (2ml).Add isobutyl-boric acid (60mg, 0.57mmol, 3 equivalents) and HCl 4N 1,4-diox (0.07ml, 0.28mmol, 1.5 equivalents) to this solution.Stirred 20 hours under the gained bifasic mixture room temperature, shift out the n-hexane, methanol solution is with n-hexane (2ml) washing, and vapourisation under reduced pressure.Crude product is suspended in Anaesthetie Ether/n-hexane/4ml), stir under the room temperature, filters, and obtains white powder.Yield 65%, 69mg.

Analytical data: M.p.145-150 ℃.

¹H?NMR(MeOD-d4)：9.3(1H，s)；8.85(1H，s)；8.75(1H，s)；7.8(2H，d)；7.3(2H，d)；5.1(2H，t)；4(2H，dd)；2.8(1H，t)；2.75(2H，t)；1.65(3H，m)；1.4(4H，m)；1.0(3H，t)0.9(6H，dd)。

Other compounds according to the foregoing description step preparation E.5 are listed in table E-5.

Table E-5

Embodiment F .1

Decyl amide, N-[(1S)-1-[[[(1R)-1-[(4R, 5R)-4, the borolan-2-yl is disliked in 5-dicyclohexyl-[1,3,2] two]-the 3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl] amino] butyl]-

Chirality

To the boric acid that E.2 obtains like embodiment; [(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(decanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-; (125mg; 0.26mmol) Anaesthetie Ether (0.5ml) and the suspension-s of methylene dichloride (1ml) mixture, add several methyl alcohol, dissolve fully up to solid.(1R, 2R)-1, (61mg's 2-dicyclohexyl-1 0.26mmol), and at room temperature stirred the mixture 5 hours in adding.Reaction mixture is concentrated into drying, and residue is through column chromatography (silica gel) purifying, with 50: 50 ETHYLE ACETATE: the hexanes mixtures wash-out.Then, product grinds with hexane, and removes solvent through decant.Repeat to grind twice.Obtain waxy solid product (65mg, yield 37%) .M.p.75-100 ℃.

¹H?NMR(DMSO-d ₆)：8.99(1H，d，J＝2.5Hz)；8.52(1H，br)；7.98(1H，d，J＝8.05)；7.88(2H，br)；3.48(2H，d，J＝5.7)；3.14(2H，m)；2.55(1H，m)；2.19(1H，m)；2.10(2H，m)；1.79(2H，m)；1.74-1.35(16H，m)；1.24(22H，m)；1.12(5H，m)；0.89(4H，m)；0.84(9H，m)。

Embodiment F .2

The 4-phenylbutanamides, N-[(1S)-1-[[[(1R)-and 1-[13,15-two evil-14-bora-, two spiral shells [5.0.5.3]-pentadecane-14-yl]-3-methyl butyl] amino] carbonyl]-4-[[imino group (nitro amino) methyl]-amino] butyl]-

According to the foregoing description step F.1, utilize suitable boric acid parent material and dicyclohexyl-1,1 '-glycol, preparation title compound.

Analytical results: ¹H NMR (DMSO-d ₆): 8.79 (1H, d, J=2.5Hz); 8.52 (1H, br); 8.00 (1H, d, J=7.94); 7.85 (2H, br); 7.31-7.23 (2H, m); 7.20-7.14 (3H, m); 4.40-4.30 (1H, m); 3.15 (2H, m); 2.55 (3H, m); 2.14 (2H, t, J=7.3Hz); 1.78 (2H, q, J=7.3Hz); 1.70-0.97 (27H, m); 0.84 (3H, t, J=6.7Hz); 0.83 (3H, t, J=6.7Hz).

Embodiment F .2.1

The 4-butyl benzamide, N-[(1S, 2R)-1-[[[(1R)-and 1-[13,15-two evil-14-bora-, two spiral shells [5.0.5.3] pentadecane-14-yl]-3-methyl butyl] amino] carbonyl]-the 2-hydroxypropyl]-.

Chirality

According to the foregoing description step F.1, utilize suitable boric acid parent material and dicyclohexyl-1,1 '-glycol, the preparation title compound.

Analytical results: ¹H NMR (DMSO-d ₆): 8.98 (1H, s br.); 8.00 (1H, d, J=8.5); 7.81 (2H, d, J=8.2); 7.31 (2H, d, J=8.2); 5.03 (1H, d, J=6.2); (4.49 1H, dd, J=8.5,5.0); 4.07-3.98 (1H, m); 2.64 (1H, t, J=7.6); 2.57-2.50 (1H, m); 1.65-1.21 (21H, m); 1.14-1.00 (9H, m); 0.90 (3H, t, J=7.4); (0.85 6H, d, 6.5).

Embodiment G.1

10-(1,3-dioxy-1,3-dihydro-isoindole-2-yl)-capric acid.

Step 1:2-11-10-thiazolinyl-1,3-dioxy-1,3-xylylenimine

To 10-hendecene-1-alcohol (4.23g; 24.8mmol), phthalimide (3.65g, 24.8mmol) and triphenylphosphine (6.51g; 24.8mmol) the mixture of anhydrous tetrahydro furan (30ml); (3.9ml, anhydrous tetrahydro furan 24.8mmol) (10ml) solution keep temperature to be lower than 8-10 ℃ simultaneously slowly to add DEAD.After 2 hours, other add DEAD (1.0ml, 6.37mmol) and triphenylphosphine (1.3g 4.96mmol), stirs the mixture under the room temperature and spends the night.Reaction mixture concentrates, and residue grinds with Anaesthetie Ether (50ml).Solid by filtration shifts out, and with Anaesthetie Ether (2 * 50ml) washings.The filtrating that merges concentrates, and residue grinds down for 40 ℃ with hexane (50ml).The gained solid by filtration shifts out, and with hexane wash (2 * 50ml).The filtrating that merges concentrate and residue through column chromatography purification, with 10: 2 hexanes: the ethyl acetate mixture wash-out.Obtain the product (4.9g, yield 66%) of lower melting point white solid.M.p.25-30℃。

¹H?NMR(DMSO-d ₆)7.83(4H，m)；5.76(1H，m)；4.96(1H，dq，J＝17.2，1.6Hz)；4.90(1H，ddt，J＝10.2，2.2，1.1)；3.54(2H，t，J＝7.1)，1.97(2H，q，J＝6.7)；1.56(2H，m)；1.35-1.15(14H，m)。

Step 2:10-(1,3-dioxy-1,3-xylylenimine-2-yl) capric acid

2-11-10-thiazolinyl-1 with step 1; 3-dioxy-1; 3-xylylenimine (2g; 6.68mmol) and the hexane (20ml) of Aliquat

336 (0.2g) and the solution of acetate (6ml) mixture dropwise be added to potassium permanganate (2.76g; Water 20mmol) (28ml) solution is simultaneously 0 ℃ of cooling.Stirred 7 hours under the reaction mixture room temperature, add aqueous solution of sodium bisulfite then, disappear up to purple.Then, mixture is with ethyl acetate extraction, and organic phase is to dried over sodium sulfate and concentrated.Residue is through the silica gel column chromatography purifying, with 2: 1 hexanes: the ethyl acetate mixture wash-out.Obtain the product (1.29g, yield 61%) of white solid.M.p.58-60℃。

¹H?NMR(DMSO-d ₆)11.95(1H，br)；7.85(4H，m)；3.55(2H，t，J＝7.2Hz)；2.17(2H，t，J＝7.2Hz)；1.7-1.4(4H，m)；1.22(10H，m)。

Embodiment G.2

6-(phenylsulfonamido) caproic acid

(2.5ml, (1g, (22ml) is with diox (3ml) solution, simultaneously 0-5 ℃ of stirring for 2N NaOH 7.62mmol) 19mmol) to be added to 6-aminocaprolc acid with benzene sulfonyl chloride.Let mixture heat, and stirred 1 hour to room temperature.Reaction mixture is acidified to pH 2 with 37% spirit of salt then with ETHYLE ACETATE (50ml) washing, and with ethyl acetate extraction (2 * 50ml).The organic layer that merges is to dried over sodium sulfate and concentrated.Residue grinds with hexane.Through solid collected by filtration, and dry down in 50 ℃ in vacuum, obtain 1.1g title compound (yield 55%).

M.p.113-115℃。

¹H?NMR(DMSO-d6)：11.96(1H，s)；7.79(2H，m)；7.60(4H，m)；2.71(2H，m)；2.13(2H，t，J＝7.14Hz)；1.38(4H，m)；1.21(2H，m)。

Embodiment G.3

6-(ethyl sulfonamido) caproic acid

(3.9ml, 41.1mmol) De diox (10ml) solution is added to 6-aminocaprolc acid (2g, (56ml) is with diox (10ml) solution, simultaneously 0-5 ℃ of stirring for 1N NaOH 15.2mmol) with ethyl sulfonyl chloride.The pH of reaction mixture is adjusted to 8-9 through adding 25% sodium hydroxide solution.Let mixture heat, and stirred 30 minutes to room temperature.Other adds 25%NaOH solution to regulate pH to about 11.3.5 after hour, add 1N spirit of salt (15ml) and ETHYLE ACETATE (60ml).Organic layer is to dried over sodium sulfate and concentrated.Residue grinds with the mixture of Anaesthetie Ether (5ml) and hexane (15ml).Solid by filtration is collected and is dry, obtains 1.3g title compound (yield 40%).

¹H?NMR(DMSO-d6)：11.9(1H，s)；6.97(1H，t，J＝5.7Hz)；2.97(2H，q，J＝7.1)；2.88(2H，q，J＝6.6)；2.2(2H，t，J＝7.3)；1.47(4H，m)；1.29(2H，m)；1.18(3H，t，J＝7.3)。

Embodiment G.4

8-(ethyl sulfonamido) is sad

(1.5ml, 15.7mmol) De diox (5ml) solution is added to the 8-aminocaprylic acid (1g, (22ml) is with diox (5ml) solution, simultaneously 0-5 ℃ of stirring for 1N NaOH 6.28mmol) with ethyl sulfonyl chloride.Let mixture heat, and stirred 3.5 minutes to room temperature.In this stage,, regulate pH to 7-8 through adding 25%NaOH solution with 1 hour interval.Reaction mixture washs with Anaesthetie Ether (30ml).Regulate pH to 1-2 through adding 1N HCl, and with ETHYLE ACETATE (70ml) extraction mixture.Organic layer is to dried over sodium sulfate and concentrated.Residue grinds with the mixture of Anaesthetie Ether.Through solid collected by filtration, and dry under vacuum, obtain 600mg title compound (yield 38%).

¹H?NMR(DMSO-d6)：11.9(1H，s)；6.96(1H，t，J＝6Hz)；2.96(2H，q，J＝7.1)；2.88(2H，q，J＝6.6)；2.2(2H，t，J＝7.3)；1.45(4H，m)；1.26(6H，m)；1.18(3H，t，J＝7.3)。

Embodiment G.5

3-amino-2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-propionic acid, benzyl ester.

Step 1:N-t-butoxy carbonyl-altheine [commercially available]

(12g 0.113mol) is dissolved in water (225ml) and 1,4-diox (225ml) under the room temperature for altheine (15g, 0.113mol, 1 equivalent) and yellow soda ash.Add two-tert-butyl-two carbonic ether (30g, 0.137mol, 1.2 equivalents) to this solution, and stir the mixture and spend the night.Evaporating solvent is up to 1 down in decompression, and the distillation of 4-diox is regulated pH to 2 with HCl 37%, obtains white solid, after the filtration, with water washing and dry.Yield 91%.24g。

Analytical data: m.p.175-180 ℃ (lit.175 ℃).

¹H?NMR(DMSO-d ₆)12.5(1H，br)；7.31(1H，br)；6.91(1H，br)；6.87(1H，d，J＝8.4Hz)；4.23(1H，q，J＝7.7Hz)；2.56-2.36(2H，m)；1.38(9H，s)。

Step 2:N-[(1,1-dimethyl-ethoxy carbonyl) amino]-altheine, benzyl ester.

According to Bioorg.Med.Chem., 6 (1998) 1185-1208 prepare compound.The N-of step 1 [(1,1-dimethyl-ethoxy carbonyl) amino]-altheine (20.7g, 89.1mmol, 1 equivalent) is dissolved in methyl alcohol (500ml), and adds cesium carbonate (15.97g, 49mmol, 0.55 equivalent).Evaporating solvent obtains white solid, is dissolved in N, dinethylformamide (200ml).Dropwise add benzyl bromide (11.6ml, 98mmol, 1.1 equivalents) to suspension-s, and stir the mixture and spend the night.Solvent is reduced, add entry (300ml), with ETHYLE ACETATE (200ml) extraction mixture; With salt solution (50ml) washing, and shift out solvent under the decompression, obtain crude product; Be suspended in n-hexane (160ml), filtration is also dry under vacuum, obtains the 14.68g white solid.Yield 51%.

Analytical data: m.p.113-115 ℃.

¹H?NMR(DMSO-d ₆)7.35(6H，m)；7.13(1H，d，J＝7.9Hz)；6.94(1H，br?s)；5.10(2H，s)；4.39(1H，q，J＝7.4Hz)；2.6-2.4(2H，m)；2.03(2H，t，J＝7.3)；1.37(9H，s)。

Step 3:3-amino-2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-propionic acid, benzyl ester.

The N-of step 2 [(1,1-dimethyl-ethoxy carbonyl) amino]-altheine, benzyl ester, (2g, 6.3mmol, 1 equivalent) is dissolved in acetonitrile (80ml) and water (80ml).Solution is cooled to 0-5 ℃, and branch adds iodobenzene diacetate ester (3g, 9.3mmol, 1.5 equivalents).Mixture stirred the mixture 30 minutes at 0 ℃, stirred 4 hours under the room temperature then.Shift out under the organic solvent vacuum, add Anaesthetie Ether and HCl 1N.Separate the waterbearing stratum, and with methylene dichloride (100ml) and sodium hydrogencarbonate (3.5g) extraction.Organic solvent is to anhydrous sodium sulfate drying, and decompression evaporation down obtains the 0.65g water white oil.Yield 36%.

Analytical data:

¹H?NMR(DMSO-d ₆)7.45-7.20(7H，m)；7.20(1H，d，J＝7.7Hz)；5.13(2H，AB?q，J＝12.8)；4.01(1H，m)；2.80(2H，m)；1.38(9H，s)。

Embodiment G.6

(2S)-2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-[(4-methyl benzoyl) amino] propionic acid.

Step 1:2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(the 4-toluyl is amino) propionic acid, benzyl ester.

Embodiment 3-amino-2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-propionic acid G.5, benzyl ester, (690mg, 2.34mmol, 1 equivalent) is dissolved in dry DMF (20ml), adds TBTU (900mg, 2.98mmol, 1.2 equivalents).Stirred 10 minutes under the mixture room temperature, be cooled to 0-5 ℃, add NMM (0.51ml, 4.68mmol, 2 equivalents) and 4-tolyl acid (380mg, 2.81mmol, 1.2 equivalents) with ice bath.Stirred the mixture under the room temperature 3 hours, and be poured into water (100ml), and extract with ETHYLE ACETATE (100ml).Organic layer is with Hydrocerol A 2% (50ml), sodium hydrogencarbonate 2% (50ml), and the solution washing of NaCl 2% (50ml), to anhydrous sodium sulfate drying, decompression is evaporation down, obtains 1g oil.Quantitative yield.

Analytical data:

¹H?NMR(DMSO-d ₆)8.46(1H，br?t，J＝5.7Hz)；7.70(2H，d，J＝8.0)；7.35-7.2(8H，m)；5.07(2H，s)；4.29(1H，m)；3.67(1H，m)；3.58(1H，m)；2.36(3H，s)；1.37(9H，s)。

Step 2: (2S)-2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(the 4-toluyl is amino) propionic acid.

The 2-S-of step 1 [(1,1-dimethyl-ethoxy carbonyl) amino]-3-(the 4-methyl benzoyl is amino)-propionic acid, benzyl ester, (930mg 2.25mmol), is dissolved in methyl alcohol (25ml), and adds Pd/C 10% (90mg).Mixture is hydrogenation 1 hour under atmospheric pressure.Filter Pd/C, decompression is evaporating solns down, obtains the 650mg white foam.Yield 86%.Analytical data:

¹H?NMR(DMSO-d ₆)：12.5(1H，br)；8.40(1H，t，J＝5.7Hz)；7.71(2H，d，J＝8.05Hz)，7.27(2H，d，J＝8.05Hz)；7.09(1H，d，J＝7.9)，4.17(1H，m)；3.57(2H，m)；2.35(3H，s)；1.37(9H，m)。

Embodiment G.7

2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(hexanamido) propionic acid.

Step 1:2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(caproyl is amino) propionic acid, benzyl ester.

Caproic acid (450mg, 3.87mmol, 1.2 equivalents) is dissolved in dry DMF (15ml), and adds TBTU (1.24g, 3.87mmol, 1.2 equivalents), stirs the mixture under the room temperature 20 minutes, is cooled to 0-5 ℃ with ice bath then.Add embodiment 3-amino-2-S-[(1,1-dimethyl-ethoxy carbonyl) amino] propionic acid G.5, benzyl ester (950mg, 3.22mmol, 1 equivalent) and NMM (1.06ml, 9.61mmol, 2.5 equivalents).Stir the mixture under the room temperature and spend the night, be poured in the water (150ml), and extract with ETHYLE ACETATE (100ml).Organic layer is with Hydrocerol A 2% (50ml), sodium hydrogencarbonate 2% (50ml), the solution washing of NaCl 2% (50ml); To anhydrous sodium sulfate drying, decompression evaporation down obtains crude product; (eluent: n-hexane/ethyl acetate 2/1, R.f=0.52) purifying obtains the 0.5g water white oil through silica gel column chromatography.Yield 40%.

Analytical data:

¹H?NMR(DMSO-d ₆)。

δ _H：7.87(1H，br?t，J＝6.2Hz)；7.35(5H，m)；7.14(1H，d，J＝8.2)；5.07(2H，s)；4.14(1H，m)；3.37(2H，m)；2.00(2H，t，J＝7.1)；1.43(2H，m)；1.36(9H，s)；1.3-1.1(4H，m)；0.83(3H，t，J＝7.1Hz)。

Step 2:2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(caproyl is amino) propionic acid.

The 2-S-of step 1 [(1,1-dimethyl-ethoxy carbonyl) amino]-3-(caproyl is amino) propionic acid, (500mg 1.27mmol) is dissolved in methyl alcohol (15ml) to benzyl ester, adds Pd/C 10% (50mg).Hydrogenation is 1 hour under the mixture normal atmosphere.Filter Pd/C, decompression is evaporating solns down, obtains the 300mg white solid.Yield 78%.

Analytical data: m.p.123-125 ℃.

¹H?NMR(DMSO-d ₆)。

δ _H：12.6(1H，br)；7.84(1H，br?t)；6.87(1H，d，J＝7.5Hz)；4.00(1H，m)；3.32(2H，m)；2.04(2H，t，J＝7.5)；1.47(2H，m)；1.38(9H，s)；1.3-1.1(4H，m)；0.85(3H，t，J＝7.1Hz)。

Embodiment G.8

Uncle 2-S--butoxy carbonyl amino-3-(4-fluorine sulfonamido) propionic acid.

Step 1:2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(4-fluorine sulfonamido) propionic acid, benzyl ester.

Embodiment 3-amino-2-S-[(1,1-dimethyl-ethoxy carbonyl) amino] propionic acid G.5, benzyl ester (1.25g, 4.24mmol, 1 equivalent) is dissolved in anhydrous methylene chloride (20ml), and under nitrogen, makes solution be cooled to 0-5 ℃.The anhydrous methylene chloride (10ml) that adds TEA (0.65ml, 4.67mmol, 1.1 equivalents) and 4-fluoro-SULPHURYL CHLORIDE (0.9g, 4.67mmol, 1.1 equivalents).Stirred 1 hour under the mixture room temperature, decompression evaporation down, and add Anaesthetie Ether (25ml), and obtain white solid, filter, dry under the vacuum, obtain the 1.89g product.

Yield 99%.

Analytical data: m.p.105-107 ℃.TLC silica gel (eluent: n-hexane/ethyl acetate 1/1, R.f=0.55).

¹H?NMR(PMSO-d ₆)。

δ _H：7.91(1H，t，J＝6.2Hz)；7.85(2H，dd，J＝5.3，8.8)；7.43(2H，t，J＝8.8)；7.35(5H，m)；7.15(1H，d，J＝8.2)；5.09(2H，s)；4.14(1H，m)；3.10(2H，m)；1.36(9H，s)。

Step 2:2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(4-fluorine sulfonamido) propionic acid.

The 2-S-of step 1 [(1,1-dimethyl-ethoxy carbonyl) amino]-3-(4-fluorine sulfonamido) propionic acid, (1.8g 3.98mmol.) is dissolved in methyl alcohol (30ml) to benzyl ester, and adds Pd/C 10% (180mg).Mixture is hydrogenation 1 hour under atmospheric pressure.Filter Pd/C, decompression is evaporating solns down, obtains the 1.39g water white oil.Yield 97%.

Analytical data:

¹H?NMR(DMSO-d ₆)。

δ _H：12.7(1H，br)；7.83(2H，dd，J＝5.3，8.8)；7.78(1H，br?t，J＝5.5)；7.42(2H，t，J＝8.8)；6.87(1H，d，J＝8.6)；3.99(1H，m)；3.03(2H，m)；1.36(9H，s)。

Embodiment G.9

2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3,4-Dimethoxyphenyl kharophen)-propionic acid.

Step 1:2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3,4-Dimethoxyphenyl kharophen)-propionic acid, benzyl ester.

3,4-dimethoxy-phenylacetic acid (720mg, 3.66mmol, 1.2 equivalents) is dissolved in dry DMF (20ml), and adds TBTU (1.17g, 3.66mmol, 1.2 equivalents), stirs the mixture under the room temperature 20 minutes, is cooled to 0-5 ℃ with ice bath then.Add embodiment 3-amino-uncle 2-S--butoxy carbonyl amino-propionic acid G.5, benzyl ester (0.9g, 3.05mmol, 1 equivalent) and NMM (1.0ml, 9.15mmol, 2.5 equivalents).Mixture stirred 2 hours for 0 ℃, was poured over then in the water (200ml), and extracted with ETHYLE ACETATE (100ml).Organic layer is used following solution washing: Hydrocerol A 2% (20ml), sodium hydrogencarbonate 2% (20ml), NaCl 2% (20ml); To anhydrous sodium sulfate drying, decompression evaporation down obtains crude product; (eluent: n-hexane/ethyl acetate 1/1, R.f=0.57) purifying obtains the 1g water white oil through silica gel column chromatography.Yield 69%.

Analytical data: ¹H NMR (DMSO-d ₆).δ _H：8.02(1H，t，J＝5.7Hz)；7.34(5H，m)；7.17(1H，d，J＝7.7)；6.82(2H，m)；6.71(1H，dd，J＝1.5，8.2)；5.03(2H，s)；4.14(1H，m)；3.71(3H，s)；3.69(3H，s)；3.39(2H，m)；1.36(9H，s)。

Step 2:2-S-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3,4-Dimethoxyphenyl kharophen)-propionic acid.

The 2-S-of step 1 [(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3,4-Dimethoxyphenyl kharophen)-propionic acid, (1g 2.1mmol.) is dissolved in methyl alcohol (30ml) to benzyl ester, and adds Pd/C 10% (10mg).Mixture is hydrogenation 1 hour under atmospheric pressure.Filter Pd/C, and vapourisation under reduced pressure solution, the 0.73g white foam obtained.Yield 91%.

Analytical data: ¹H NMR (DMSO-d ₆).δ _H：12.7(1H，br)；8.06(1H，t，J＝5.9Hz)；7.00(1H，d，J＝8.05)；6.91(2H，m)；6.80(1H，dd，J＝1.5，8.4)；4.08(1H，m)；3.80(3H，s)；3.78(3H，s)；3.5-3.3(2H，m)；1.36(9H，s)。

Embodiment G.10

2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3-phenyl urea groups) propionic acid.

Step 1:2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3-phenyl urea groups) propionic acid, benzyl ester.

Embodiment 3-amino-2-S-[(1,1-dimethyl-ethoxy carbonyl) amino] propionic acid G.5, benzyl ester (1.14g; 3.87mmol; 1 equivalent) be dissolved in methylene dichloride (20ml) under the room temperature, solution is cooled to 0-5 ℃, and dropwise adds phenyl isocyanate (0.42ml; 3.87mmol, 1 equivalent) methylene dichloride (5ml).Stirred under the solution room temperature 1 hour, decompression is evaporation down, and through silica gel column chromatography (eluent: n-hexane/ethyl acetate 1/1) purifying, obtain 0.71g hyaloid solid, be suspended in Anaesthetie Ether, obtain white solid.Yield 44%.Analytical data: TLC silica gel (eluent n-hexane/ethyl acetate 1/1R.f.=0.44), m.p.48-50 ℃.

¹H?NMR(DMSO-d ₆)。δ _H：8.68(1H，s)；7.4-7.27(8H，m)；7.22(2H，t，J＝8.2Hz)；6.90(1H，t，J＝7.3)；6.26(1H，t，J＝5.7)；5.11(2H，s)；4.12(1H，m)；3.58(1H，m)；3.28(1H，m)；1.38(9H，s)。

Step 2:2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3-phenyl urea groups) propionic acid.

The 2-S-of step 1 [(1,1-dimethyl-ethoxy carbonyl) amino]-3-(3-phenyl urea groups) propionic acid, (0.7g 1.7mmol.) is dissolved in methyl alcohol (25ml) to benzyl ester, and adds Pd/C 10% (70mg).Mixture is hydrogenation 1 hour under atmospheric pressure.Filter Pd/C, and vapourisation under reduced pressure solution, the required product of 0.47g obtained.Yield 87%.

Analytical data: ¹H NMR (DMSO-d ₆).δ _H：12.6(1H，br)；8.66(1H，s)；7.37(2H，d，J＝8.1Hz)；7.21(2H，t，J＝7.50)；7.08(1H，d，J＝7.9)；6.89(1H，t，J＝7.3)；6.21(1H，t，J＝5.9)；3.98(1H，m)；3.54(1H，m)；3.22(1H，m)；1.38(9H，s)。

Embodiment G.11

Synthesizing of other compounds

From embodiment 3-amino-2-S-[(1,1-dimethyl-ethoxy carbonyl) amino] propionic acid G.5, benzyl ester begins, and utilizes embodiment step 1 and the described method of step 2 G.6-G.10, the preparation following compounds.

Embodiment G.12

2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(the 3-benzyloxycarbonyl is amino) propionic acid.

Step 1:N ²-(uncle-butoxy carbonyl)-L-2, the 3-diaminopropionic acid

Will G.5 step 1 or commercially available uncle N--butoxy carbonyl-altheine (8g, 0.034mol, 1 equivalent) be suspended in ETHYLE ACETATE (72ml) from embodiment; In acetonitrile (72ml) and the water (36ml), and 5 ℃ add down the iodobenzene diacetate esters (13,3g; 0.041mol, 1.2 equivalents).Mixture stirred 3-4 hour down at 10-25 ℃, occurred white solid then.Solids filtered, with the Anaesthetie Ether washing, and dry under vacuum, obtain white powder.Yield 57%.4g。

Analytical data: m.p.210-211 ℃.Silica gel (methylene chloride/acetate 5/3/1) Rf0.5. ¹H?NMR(DMSO-d ₆)4.15(1H，t)；3.15(2H，m)；1.45(9H，s)；

Step 2:2-[(1,1-dimethyl-ethoxy carbonyl) amino]-3-(the 3-benzyloxycarbonyl is amino) propionic acid.

The N of step 1 ²-(uncle-butoxy carbonyl)-L-2, the 3-diaminopropionic acid is dissolved in aqueous sodium carbonate 10% (2.2 equivalent) and 1,4-diox (38ml) under (3,8g, 0,018mol, 1 equivalent) 25 ℃.In this solution, dropwise add benzyl chloride manthanoate (3ml, 0,020mol, 1.1 equivalents), solution stirred 3 hours down for 25 ℃.When reaction finished, mixture was poured over water (100ml), and washs with Anaesthetie Ether (100ml).Add HCl 37% (6ml) to this aqueous solution, up to pH2, the mixture of gained extracts with ETHYLE ACETATE (100ml).Separate organic layer, use brine wash, and to anhydrous sodium sulfate drying.Shift out solvent under the decompression, obtain water white oil, obtain white foam under the vacuum.Yield 93%, 5.9g.

Analytical data: silica gel (methylene chloride/acetate 5/3/1) Rf 1.

¹H?NMR(DMSO-d ₆)12.6(1H?br?s)；7.35(5H?m)；6.94(1H，d)；5(2H，s)；4.1(2H，m)；1.4(9H，s)。

Embodiment G.13

2-(uncle-butoxy carbonyl is amino)-3-pyrazol-1-yl-propionic acid.

According to Vederas, J.Am.Chem.Soc, 1985,107, the step described in the 7105-7109 prepares midbody.

Embodiment G.14

1-methylsulfonyl-piperidines 4-carboxylic acid

Step 1:1-[(1,1-dimethyl-ethoxy carbonyl) amino]-piperidines-4-carboxylic acid

Piperidines 4-carboxylic acid (5g, 38.7mmol, 1 equivalent) is dissolved in sodium carbonate solution (4.5g, 42.61mmol, 2.2 equivalents), 70ml and 1,4-diox (30ml).Dropwise add 1 of two-tert-butyl, two carbonic ethers (9.3g, 42.61mmol, 1.1 equivalents), 4-diox (40ml) solution, stirred overnight under the gained mixture room temperature.Shift out under the organic solvent decompression, gained solution with the HCl37% acidifying up to pH2.Filter gained suspension-s, with Anaesthetie Ether (5ml) washing white solid.Mother liquor extracts with ETHYLE ACETATE (120ml), and adds previous solid.Organic solution is to anhydrous sodium sulfate drying, and decompression evaporation down obtains white solid, and 80 ℃ of following vacuum-dryings obtain title compound.Yield 93%, 8.2g.

Analytical data: m.p.133-135 ℃.

¹H?NMR(DMSO-d ₆)12.3(1H?br?s)；3.85(2H，d)；2.8(2H，br)；2.35(1H，t)；1.8(2H，d)；1.4(11H，m)。

Step 2:1-[(1,1-dimethyl-ethoxy carbonyl) amino]-piperidines-4-carboxylic acid benzyl ester

The 1-of step 1 [(1,1-dimethyl-ethoxy carbonyl) amino]-piperidines-4-carboxylic acid (6g, 26.16mmol, 1 equivalent) is dissolved in the methyl alcohol (150ml), adds cesium carbonate (4.26g, 13.08mmol, 0.5 equivalent).Stirred the mixture under the room temperature 2 hours, and shifted out solvent under the decompression.Crude product is dissolved in DMF (100ml), dropwise adds benzyl bromide (5.37g, 31.39mmol, 1.2 equivalents).Stirred overnight under the mixture room temperature, and be poured over water (300ml), extract with ETHYLE ACETATE (900ml).Organic layer is to anhydrous sodium sulfate drying, and vapourisation under reduced pressure, obtains white solid.Yield 95%, 7g.

Analytical data:

¹H?NMR(DMSO-d ₆)7.3(5H?m)；5.1(2H，s)；3.85(2H，d)；2.8(2H，br)；2.65(1H，t)；1.8(2H，d)；1.4(11H，m)。

Step 3: piperidines-4-carboxylic acid benzyl ester, hydrochloride.

[(1,1-dimethyl-ethoxy carbonyl) amino]-(7g 21.0mmol) is dissolved in 1 to piperidines-4-carboxylic acid benzyl ester to the 1-of step 2,4-diox (20ml).Add 1 of HCl 4N, 4-diox (7.8ml, 300ml, 12 equivalents), stirred overnight under the gained solution room temperature to this solution.Solids filtered is suspended in n-hexane (50ml), and filtration obtains white solid.Yield 54%, 2.5g.

Analytical data:

¹H?NMR(DMSO-d ₆)8.9(2H，br)；7.35(5H，m)；5.1(2H，s)；3.25(2H，d)；2.9(2H，t)；2.75(1H，m)；2.0(2H，m)；1.8(2H，m)。

Step 4:1-methylsulfonyl-piperidines-4-carboxylic acid benzyl ester.

The piperidines of step 3-4-carboxylic acid benzyl ester, hydrochloride (1g, 3.9mmol, 1 equivalent) is dissolved in DMF (15ml), adds triethylamine (0.55ml, 4mmol, 1 equivalent) and methylsulfonyl chloride.Stirred 1 hour under the mixture room temperature, be poured over then in the water (20ml).The aqueous solution is with ETHYLE ACETATE (90ml) extraction, and organic layer is to anhydrous sodium sulfate drying, and decompression evaporation down obtains water white oil.Yield 78%, 0.9g.

Analytical data:

¹H?NMR(DMSO-d ₆)7.35(5H，m)；5.1(2H，s)；3.5(2H，d)；2.8(5H，m)；2.6(1H，m)；2.0(2H，m)；1.6(2H，m)。

Step 5:1-methylsulfonyl-piperidines 4-carboxylic acid

(0.8g 26.7mmol) is dissolved in ETHYLE ACETATE (100ml) and methyl alcohol (10ml) to the 1-methylsulfonyl-piperidines of step 4-4-carboxylic acid benzyl ester, adds Pd/C 10% (80mg), hydrogenation under gained mixture 1 bar pressure.Catalyzer filters Celite, shifts out solvent under the decompression, obtains white solid.Yield 73%, 0.4g.

Analytical data:

¹H?NMR(DMSO-d ₆)12.4(1H，br)；3.6(2H，d)；2.9(4H，m)；2.4(1H，m)；2.0(2H，m)；1.6(2H，m)。

Embodiment G.15

(4-aminomethyl phenyl)-urea groups SULPHURYL CHLORIDE

According to J.Med, Chem.1996,39,1243-1252 prepares this compound.In brief, with anhydrous Anaesthetie Ether dilution Sulfuryl chloride isocyanate (1.62g, 11.5mmol, 1 equivalent) solution, ℃ cooling of gained solution in-50 ℃＜T＜-40.Add p-Tolylamine (1.23g, 11.5mmol, 1 equivalent) to this solution.Solution stirred 10 minutes at-35 ℃, obtained suspension-s.Solids filtered is washed with Anaesthetie Ether.Yield 80%, 2.3g.

Analytical data: m.p.127-129 ℃.

¹H?NMR(DMSO-d ₆)9.9(1H，s)；7.3(2H，d)；7.1(2H，d)；2.25(3H，s)；

Embodiment G.16

Isoxazole-5-carboxylic acid

According to Wolfang etc., Synthesis, 1986, the said step of 69-70 prepares required carboxylic acid.

Practicality

Compound activity

Compound arrestin enzyme body of the present invention is active.Following table F-1 for example, the active ability of arrestin enzyme body is just about providing the data relevant with several example compound of the present invention.

Method and composition

Compound of the present invention can arrestin enzyme body activity, cause suppressing or block directly or indirectly relevant endocellular function of multiple and proteasome.For example, proteasome inhibitor can be regulated and control, for example the apoptosis of inducing cell.In some embodiments, the compound here can be through apoptosis-induced and kill tumor cell.Therefore, The compounds of this invention can be used to treat cancer, tumour or other propagation imbalances.

In other embodiment, can suppress the activation or the processing of transcription factor NF-KB through The compounds of this invention arrestin enzyme body function.This albumen plays a role in the regulation and control of the gene that relates to immunity and inflammatory reaction and cell survival.The inhibition of proteasome function also suppresses ubiquitin/proteolyze approach.This approach is highly unusual albumen and the short life modulin of catalytic selectivity degraded especially.In some embodiments, compound of the present invention can prevent usually by the degraded of the p53 of the approach degraded of ubiquitin dependence.Ubiquitin/proteolyze approach also relates to the cell of endocytosis or virus antigen is processed into the antigenic peptide that is attached to the MHC-I molecule.Therefore, compound of the present invention can be used to reduce the activity of the proteolyze system that the kytoplasm ATP-ubiquitin of many cell types relies on.

Therefore, the use of these compounds comprises treatment, for example treatment various diseases or the imbalance relevant with proteasome.Method comprises Mammals, for example suffers from The compounds of this invention or its compsn with people's drug treatment significant quantity of proteasome diseases associated or imbalance." treatment significant quantity " refers to be enough to prevent, alleviates or improve any phenomenon, the cause relevant with disease or imbalance for example known in the art or the amount of symptom.

Medicable disease or imbalance (unusual physical appearance) can be relevant with normal or unusual proteasome activity, for example regulation of apoptosis.Numerous relevant with proteasome or through apoptosis-induced and disease or imbalance desirably treatment are known, and for example comprise that various cancers and tumour comprise and skin, prostate gland; Colorectum, pancreas, kidney, ovary, mammary gland; Liver, tongue, lung, those diseases relevant with smooth muscle tissue.Preferably can include but not limited to neoplastic hematologic disorder, white blood disease for example, lymphoma, non--He Jiejin lymphomas through the tumour that proteasome inhibitor is treated; Myelomatosis, and multiple myeloma, and solid tumor, for example colorectum knurl; Mastadenoma, prostate tumor, lung knurl and Vipoma.Be to cause result of treatment, proteasome inhibitor can be used as single medicament or with one or more antitumor or antitumor and anticancer agent and/or radiotherapy combination medicine-feeding to patient.Other can be advantageously include but not limited to Zorubicin, daunomycin, methotrexate, vincristine(VCR) with the example of the antitumor or carcinostatic agent of proteasome inhibitor concomitant dosing; Ismipur, cytarabin, endoxan, 5-FU, hexamethyl trimeric cyanamide; Carboplatin, cis-platinum, idarubicin, taxol, Japanese yew terpene; NSC 94600, Rinotecan, gemcitabine, L-PAM, BCNU and VP-16.The method of external test apoptosis is well known in the art, and test kit can commerce be buied.Referring to for example from Promega company, Madison WI, the Apo-ONE of USA ^TMHomogeneous phase Caspase-3/7 analyzes (technological notification number 295,2/02 is revised Promega company).

Other diseases relevant with proteasome or imbalance are included in acceleration or the enhanced proteolyze that takes place in the muscle of atrophy, and be for example relevant with the activation of the non-lysosome ATP of the need that comprise ubiquitin process usually.Acceleration or enhanced proteolyze can be results any in numerous causes, and reason comprises pyemia, burn, wound; Cancer infects neurodegenerative disease, for example muscular dystrophy; Acidismus or spinal cord/nerve injury, the use of sterol hormone, fever, stress and hungry.Compound of the present invention can be through any method known in the art, for example the homaluria through measuring the amino acid 3-Methyl histidine of modifying (referring to, as; Young etc., Federation Proc., 1978; 37,229), detect restraining effect to muscle loss.

Compound of the present invention also can be further used for treatment or prevent and NF-kB activity diseases associated or imbalance, for example comprises, human immunodeficiency virus (HIV) infects and from for example, transplant rejection; Sacroiliitis infects inflammatory enteritis; Asthma, osteoporosis, osteo-arthritis; Psoriasis, the inflammatory imbalance of restenosis and autoimmune disease.Therefore, the activatory method that prevents to suffer from NF-κ B among the patient of above-mentioned disease will be that treatment is gone up favourable.The inhibition of NF-kB activity can be through for example using Palombella etc., Cell, and 1994,78, the 773 DNA binding analysis described are measured.

Use standard diagnostics technology, those skilled in the art easily identify and are easy to or suspect the individuality of suffering from this disease or imbalance.

Embodiment A

The active analysis of 20S HRBC proteasome (HEP) chymotrypsin-like

Proteasome chymotrypsin-like according to following methods analyst The compounds of this invention is active.

In the microtiter plate of 96-hole, with the 0.04%SDS 20mM Tris damping fluid tiling of 0.2 μ g/mL (approximately 0.6nM catalytic site) available from Immatics Biotechnologies Inc., Tubingen, the 20S HRBC proteasome (HEP) of Germany.Available from Sigma Inc., St.Louis, MO, it is 100 μ M that the fluorometric assay substrate Suc-LLVY-AMC of USA (succinyl--Leu-Leu-Val-Tyr-7-amino-4-methylcoumarin) adds final concentration to from the methyl-sulphoxide storage liquid of 10mM.Reaction volume is every hole 100 μ L.37 ℃ hatch different time after, on Perkin Elmer HTS 7000Plus microtiter plate plate reading machine, measure the concentration of free AMC (amino methyl tonka bean camphor) with 370nM excitation wavelength and 465nM emission wavelength.Substrate hydrolysis linear in time increase and the proportional condition of concentration of the change of fluorescent signal and free AMC under measure proteasome activity.

Embodiment B

The analysis of α chymotrypsin activity

In the microtiter plate of 96-hole, with the 0.5MNaCl 50mM Hepes damping fluid tiling of 10ng/mL (approximately 2pM catalytic site) ox alpha-chymotrypsin available from Sigma Inc..Available from Sigma Inc., St.Louis, MO, it is 25 μ M that the fluorometric assay substrate Suc-AAPF-AMC of USA (succinyl--Ala-Ala-Pro-Phe-7-amino-4-methylcoumarin) adds final concentration to from the methyl-sulphoxide storage liquid of 10mM.Reaction volume is every hole 100 μ L.After the incubated at room different time sections, on Perkin Elmer HTS 7000Plus microtiter plate plate reading machine, measure the concentration of free AMC with 370nM excitation wavelength and 465nM emission wavelength.Mensuration α chymotrypsin activity under the linear in time proportional condition of concentration that increases with the change of fluorescent signal and free AMC of substrate hydrolysis.

Embodiment C

HEP and alpha-chymotrypsin suppressor factor IC ₅₀The mensuration of value

IC ₅₀Value is generally defined as enzymic activity is produced the necessary compound concentration of 50% inhibition.IC ₅₀Value is that compound is to its active useful indicators that earmarks.If proteasome inhibitor of the present invention is for the IC that suppresses HRBC's proteasome (HEP) ₅₀Value is less than about 1 μ mol, and then this suppressor factor can be thought activated.In some embodiments, this suppressor factor shows for some specificitys of HEP and the IC of inhibition ox alpha-chymotrypsin ₅₀With respect to the IC that suppresses HEP ₅₀Ratio, i.e. IC ₅₀(alpha-chymotrypsin)/IC ₅₀(HEP), greater than about 100.

As far as the active inhibition of chymotrypsin-like of HEP and ox alpha-chymotrypsin through the supposition suppressor factor of enzyme and various concentration was hatched and was measured in 15 minutes at 37 ℃ (or be room temperature for the α Quimotrase) before adding substrate.Three parts of each experiment condition repeat assessment, and suppressor factor described herein carried out repeated experiments.

In the analysis of above-mentioned evaluation, if suppress the IC of HEP ₅₀Value is less than 1000nM, and compound then of the present invention can be thought activated.Preferred compound of the present invention suppresses the IC of HEP ₅₀Value is less than 100nM.Compound more preferably of the present invention suppresses the IC of HEP ₅₀Value can be less than 10nM.Compound of the present invention has shown the IC that suppresses HEP in the analysis of above-mentioned evaluation ₅₀Value is less than 1000nM.

Embodiment D

Active to the active cell analysis of proteasome chymotrypsin-like in Molt-4 clone according to following method analyzing proteins enzyme body chymotrypsin-like in Molt-4 cell (human leukemia).The concise and to the point description (Harding etc., J.Immunol., 1995,155,1767) of this method was disclosed in the past.

Washing Molt-4 cell also is resuspended in HEPES-buffered saline (5.4mM KCl, 120mM NaCl, 25mM glucose, 1.5mM MgSO ₄, the 1mM Sodium.alpha.-ketopropionate, 20mMHepes) in and with final concentration 6 * 10 ⁶Individual cells/well is tiled in the 96 hole microtiter plates.Prepare various 5 * proteasome inhibitor liquid concentrators (or the DMSO of dilution is with comparing) from 250 * DMSO solution with 50 times of HEPES-buffered saline dilutions then, add in the plate with 1 * final concentration.37 ℃ hatch 15 minutes after; Available from Enzyme Systems Products, the fluorometric assay of catalog number (Cat.No.) AFC-88 joins each hole with final concentration 25 μ M with the DMSO storage solutions of the permeable substrate of cell (MeOSuc-FLF-AFC) (methoxyl group succinyl--Phe-Leu-Phe-7-amino-4-trifluoromethyl tonka bean camphor) from 20mM.Reaction volume is every hole 100 μ l.

At Polastar Optima, use excitation wavelength 390nm and emission wavelength 520nm to detect the concentration of free AFC in per 1.5 minutes on the BMG Labtechnologies microtiter plate plate reading machine, continue 30 minutes (22 circulations).Substrate hydrolysis linear in time increase and the proportional condition of concentration of the change of fluorescent signal and free AFC under measure proteasome activity.

Embodiment E

In MOLT-4 clone, measure the EC of proteasome inhibitor ₅₀Value

EC ₅₀Value be generally defined as produce minimum and maximum response (as far as this analysis be respectively 0% and 85-90%) between the required compound concentration of halfway enzymic activity inhibition.EC ₅₀Be that compound is to its active useful indicators that earmarks.If its EC of compound of the present invention ₅₀Value then can be thought activated less than about 10 μ M.

The active inhibition of chymotrypsin-like to proteasome in the Molt-4 cell was measured through the supposition suppressor factor of cell and various concentration is hatched at 37 ℃ at the interpolation substrate before in 15 minutes.Three parts of each experiment condition repeat assessment, and suppressor factor described herein carried out repeated experiments.

In the analysis of above-mentioned evaluation, if the EC that proteasome suppresses in the MOLT-4 cell ₅₀Value is less than 10 μ M, and compound then of the present invention can be thought activated.The preferred compound of the present invention EC that proteasome suppresses in the MOLT-4 cell ₅₀Value is less than 2 μ M.The compound more preferably of the present invention EC that proteasome suppresses in the MOLT-4 cell ₅₀Value is less than 200nM.Compound of the present invention has been presented at the EC that proteasome suppresses in the MOLT-4 cell in the analysis of above-mentioned evaluation ₅₀Value is less than 10 μ M.

Embodiment F

The active analysis of proteasome trypsin-like

The proteolytic enzyme appearance activity of human proteasome can be analyzed according to the aforesaid method with following modification.In being supplemented with the Tris-glycerine damping fluid (pH 9.5) of 1mM 2 mercapto ethanol, react, and substrate can be substrate benzyloxycarbonyl--the Phe--Arg--AMC (100 μ M) for example that produces fluorescence.

37 ℃ hatch different time sections after, on Fluoro skan II spectrofluorometer, use the concentration excite filter 390nm and emission filter 460nm to detect free AMC.Substrate hydrolysis linear in time increase and the proportional condition of concentration of the change of fluorescent signal and free AMC under measure proteasome activity.

Embodiment G

Suppress the decomposition of cell muscle in the body

Suppressor factor can be through for example Tischler to the influence of rat soleus muscle loss of weight atrophy childhood, Metabolism, and the method for 1990,39,756 descriptions is measured.For example, young female Sprague-Dawley rat (80-90g) can be like Jaspers etc., J.Appl.Physiol., and 1984,57,1472 description is tail (tail-cast) fixedly, the suspention hind leg.The hind leg of animal is raised the floor that exceeds the cage house that each animal fed respectively.Animal can freely obtain food and water, and can weigh when finishing in when suspention.During suspending in midair, check that animal does not touch cage house floor with the toe point that guarantees them every day, and not by the afterbody swelling that fixedly causes.

Experimental design--first part

Each experiment begins to suspend 20 rats in midair, and these rats are divided into 4 groups, every group 5 at random.The A group is suspended 2 days, and the size of other the animal soleus muscle of baseline data to estimate the suspention longer time is provided.The mean body weight of group can relatively also be used as the correction factor of body size difference during the research beginning.Group B is another control group, and the soleus muscle of one of which limb is handled with the aqueous solution of mersalyl at loss of weight two days later, slows down amyotrophic ability to show in each treated animal loss of weight process.Behind the beginning loss of weight 2 days the time, with the aqueous solution (200nM of mersalyl; The initial body weight of 4 μ L/100g) is expelled to a soleus muscle.0.9% salt solution of the similar volume of intramuscular injection of offside (" vehicle ").Animal can use Innovar-vet (10 μ l/100g body weight) to keep calmness in the injection process in position.After the injection, animal was suspended in midair other 24 hours, took out soleus muscle.The group C and the D of each experiment are used for testing respectively two different embodiments of disclosed compound.Animal can be handled the B like group, except can be at the methyl-sulphoxide (DMSO) of the soleus muscle injection 1mM of one leg proteasome inhibitor, and only injects DMSO at the offside soleus muscle.Therefore, each experiment is made up of the test of two control groups and proteasome inhibitor of the present invention.Completion have different suppressor factor as far as 5 such experiments be 10 to detecting each suppressor factor " n " value, and each suppressor factor can be tested in the animal of different batches.

The processing of soleus muscle muscle--first part

After putting to death animal, can shred soleus muscle, reject fat and reticular tissue, and carefully weigh.Then in 10% trichoroacetic acid(TCA) (TCA) with muscle refining and pass through protein precipitation by centrifugation.Throw out washs once with 10%TCA and uses ethanol: ether (1: 1) washs once.Final resolution of precipitate is in 4ml 1N sodium hydroxide.Use the protein content of BSA through the biuret method then as the standard substance analytic sample.

Data analysis--first part

Suppressor factor mainly detects through the paired comparisons with untreated offside muscle the influence of total mytolin content.Calculate content ratio and statistical study through analyzing difference (" ANOVA ").The leg that left side leg was always handled is so the protein content ratio can also compare with untreated control animal.By this way, through comparing the relative effectivenes that the two legs protein content shows the suppressor factor of significant difference and test.Can also carry out paired student check to the effect of each individual curing.Untreated contrasting data also provides the estimated value of the 2nd day protein content.This makes to B, C, and the albumen of each group of D in 24 hours handle changes and carries out proximate calculation.

Experimental design--second section

Each experiment is made up of 10 animals, and wherein every group of a kind of suppressor factor of 5 usefulness tested it influences the albumen synthetic.Research does not need control animal as far as this respect, because the muscle that offside DMSO handles is as the matched control of the muscle of suppressor factor processing.Each group can be injected like the description of group C and D in the first part.After the in-situ treatment 24 hours, can be in two soleus muscle muscle analyzing proteins synthetic mark (fractional rate).Each muscle can be injected and contain ³H-phenylalanine(Phe) (50mM; 1 μ Ci/ml) 0.9% salt brine solution (3.5 μ l/100g end-bodies are heavy).2/3rds muscle in the middle of downcutting after 15 minutes, and handle this muscle as follows.

The processing of soleus muscle muscle--second section

Muscle is at first in that albumen is synthetic to be contained the 0.5mM U 4527 and contained in 0.84% salt solution of 20mM NSC-1026 washing 10 minutes for catching phenylalanine(Phe) in the cell in order to stop.Then in ice-cold 2% perchloric acid of 2.5ml with muscle refining.Albumen through centrifugal collecting precipitation.Get a five equilibrium supernatant and be used for liquid scintillation counting(LSC), another five equilibrium supernatant is processed phenylalanine(Phe) is converted into phenylethylamine with the soluble phenyl-alanine concentration of fluorometric assay.Referring to, like Garlick etc., Biochem.J., 1980,192,719.These values can provide intracellular specific activity.The specific activity of phenylalanine(Phe) can be through measuring behind the heating hydrolysis albumen in 6N HCl in the mytolin.The amino acid that discharges is dissolved in the damping fluid.Get a five equilibrium and be used for scintillation counting, and another five equilibrium is used to analyze the phenylalanine(Phe) of supernatant part.Albumen synthetic mark may be calculated: specific activity in albumen specific activity/cell. number of times. and the time.

Data analysis--second section

Can on the pairing basis, synthesize by analyzing proteins each suppressor factor.Whether student's paired t-test of offside muscle relatively can be measured suppressor factor synthetic influential to albumen.Proteolysis can approximately be calculated as the mark (from first part) that albumen synthetic mark (from second section) adds that albumen increases, and wherein loss of proteins produces the negative value that albumen increases.

Qualitative, suppressor factor slows down loss of proteins and do not influence albumen synthetic ability representes slowing down of proteolytic degradation.

Embodiment H

Research in the body of anti-tumor activity

Material

The proteasome inhibitor that is used for research in the body is formulated in suitable medium and is used for intravenously (iv) or oral (po) administration.For example, as far as the iv administration, compound can be dissolved in 0.9%NaCl, or for example ratio is respectively 87: 10: 3 (v: v: 0.9%NaCl v), administration in the mixture of solutol HS15 and methyl-sulphoxide.

Clone

The people of following different tissue sources and mouse tumor cell line can be used to detect the anti-tumor activity of compound of the present invention: H460 (people, lung), A2780 (people, ovary), PC-3 (people, prostate gland), LoVo (people; Colon), HCT116 (people, colon), BXPC3 (people, pancreas), PANC-1 (people, pancreas); MX-1 (people, mammary gland), MOLT (people, white blood disease), multiple myeloma (people, myelomatosis); YC8 (mouse, lymphoma), L1210 (mouse, white blood disease), 311 (mouse, lungs).

Animal species

Obtain the mouse of immunocompetent or immune anergy of 5-6 week (immunodeprived) from commercial source, for example buy from Harlan (Correzzana, Mi Italy).The CD1nu/nu mouse maintains under the aseptic condition, uses aseptic cage house, straw mattress, food and soured water.

Tumour cell is implanted and growth

The model of histological types (hystotype) (lung, ovary, mammary gland, prostate gland, pancreas, colon) solid tumor can subcutaneous (sc.) be transplanted to the arm-pit areas of immunocompetence mouse (mouse model) or immune anergy mouse (human model).Original human tumor cell line available from ATCC can be adjusted at " in the body " from " vitro culture thing " and grow into solid tumor.

The neoplastic hematologic disorder model of people or mouse can be transplanted to the different sites (iv, ip, ic or sc) of immunocompetence mouse (mouse model) or immune anergy mouse (human leukemia, lymphoma and myelomatosis model) according to their collection capacity of the highest tumour.

Drug-treated

The lotus solid tumor (stage) or the mouse of neoplastic hematologic disorder are random assignments in experimental group (10 mouse/groups).For solid tumor, each is organized average tumor weight 80-100mg and is considered to begin handle, and discards the mouse with minimum and maximum tumour.

Experimental group is by random assignment to drug-treated and control group.The oral bioavailability expenditure that depends on compound, according to following different treatment plan, animal can iv or oral processing: weekly or twice iv administration, or every day oral administration.

On solid tumor models, when (the 0th day) tumour size is in the 80-100mg scope behind the implantation tumour, begin drug-treated.

Compound can carry out administration by the volume with 10mL/ kg body weight/mouse in suitable solvent.

The anti-tumor activity parameter

Following parameters can be used for assessing anti-tumor activity:

Detect the growth of former solid tumor of each mouse through caliper measurements twice weekly;

Mouse and the comparison of control mice survival time handled;

The single mouse body weight of twice assessment weekly.

Week after the drug-treated in the end; Relative tumor growth under tumor growth inhibition TWI% (per-cent of the control group that primary tumo(u)r growth-inhibiting and media are handled) or the tumour situation is stage by stage suppressed RTWI% assesses, and calculate tumor weight as follows (TW):

TW＝1/2ab ²

Wherein a and b are the major diameter and the minor axis of tumor quality, represent with mm.

Anti-tumor activity can be determined as tumor weight and suppress (TWI%), and it calculates by following equation:

In the end a week after the drug-treated, RTWI% (relative percentage of the control group that primary tumo(u)r growth-inhibiting and media are handled) is assessed according to following equation:

Wherein

The per-cent of tumor regression can calculate by the reduction of relative tumor weight, is determined as at the tumor weight of giving the settled date divided by the initial tumor weight when experiment begins.

In the neoplastic hematologic disorder model, anti-tumor activity can be determined as mouse survival time intermediate value increases per-cent, is expressed as the ratio (T/C%) of treatment group (T) and control group (C) survival time intermediate value.Tumor free mouse does not count and is regarded as long-term survivors (LTS) when experiment finishes (transplanting back 60 days).

Toxicity assessment in the tumor-bearing mice

Can be on the basis of thick postmortem discovery and weight loss every day evaluate toxicity.When mouse death before the control animal death that media is handled, or observe when significant weight loss (＞20%) and/or spleen and liver are big or small to be reduced, be considered to die from toxic action.

Following assessment BWC% (body weight changes %):

100-(mean body weight when beginning for mouse mean body weight/processings on settled date) * 100.This value is being measured with the last all backs of handling of test compounds.

Embodiment K

The cells in vitro viability

According to following method, be determined at the IC of in-vitro measurements cell survival property under the situation that has test compounds ₅₀Value.Cell can be seeded in 96 orifice plates by different densities, after 24 hours, uses the analysis of Calcein-AM viability to measure the best whole density of each cell type then.Then cell is seeded in 96 orifice plates with the 100 μ L suitable cell culture medium well known by persons skilled in the art of measuring density.

Can carry out serial dilution so that concentration is the twice of assessment desired concn to test compounds.When 100 these diluents of μ L are added into the cell that is tiled in the 100 μ L substratum, for example can obtain final concentration, 0,11.7,46.9,187.5,375, and 750nM.Behind inoculating cell, added compound to plate in 3 to 4 hours, then with plate 37 ℃ hatch required time point (as, one, two, or three days).

Carry out the analysis of Calcein-AM viability as follows at required time point.Stay about 50 μ L/ holes after using manifold and metal sheet suction substratum.The hole with the manifold suction, stays 50 μ L/ holes with 200 μ l DPBS washing three times at every turn.Prepare the DPBS solution of 8 μ M Calcein-AM and add 150 μ L to each hole.Then plate was hatched 30 minutes at 37 ℃.After hatching, calcein can be with manifold suction and as preceding usefulness 200 μ L DPBS washing.After final suction, use Cytofluor 2300 fluorescent plate plate reading machines to measure fluorescence.Negative control can comprise substratum and not have cell, three parts of experiment repetitions.

Embodiment L

External dynamic experiment

Can use Rock etc., Cell, the proteasome of the scheme test The compounds of this invention of 1994,78,761 descriptions suppresses active.According to this method, the dissociation constant (K of equilibrium establishment when proteasome and test compounds interaction formation mixture _i).Reaction can be carried out with the SDS-activatory 20S proteasome from rabbit muscle, and the proteasome substrate is Suc-LLVY-AMC.

Embodiment M

Suppress the activation of NF-κ B

Through implementing Palombella etc., Cell, 1994,78,773 described analyses are analyzed the activity that The compounds of this invention suppresses NF-κ B.For example, MG63 osteocarcinoma cell can stimulate through handling specified number of times with TNF-α.Prepare full cell extract and use and analyze from the PRD II probe of people IFN-β gene promoter through the electrophoretic migration analysis.

Embodiment N

Compound activity

Use the analysis of the foregoing description C and embodiment E, following table F-1 shows the practicality of The compounds of this invention arrestin enzyme body.In following table, for the inhibition of HEP in the Embodiment C, have the IC of the The compounds of this invention of "+" to the HEP inhibition ₅₀Less than 1000nM; The compounds of this invention with " ++ " is less than 100nM; And the The compounds of this invention with " +++" is less than 10nM.In following table, for the inhibition of MOLT4 in the embodiment E, have the EC of the The compounds of this invention of "+" to the HEP inhibition ₅₀Less than 10000nM; The compounds of this invention with " ++ " is less than 2000nM; And the The compounds of this invention with " +++" is less than 200nM.When "＞+" occurring, active greater than the boundary of analyzing.When not showing IC ₅₀Value or EC ₅₀During value, data are still waiting to measure.

Table F-1

Embodiment #	HEP(IC ₅₀)	MOLT4(EC ₅₀)
			D.1.1	+++	+++
D.1.2	++	++
			D.1.3	+++	++
D.1.4	+++	+++
			D.1.5	+++	++
D.1.6	++	++
			D.1.7	++	+

D.1.8	+++	++
			D.1.9	++
D.1.10	++	++
			D.1.11	++	＞+
D.1.12	+++	++
			D.1.13	+++	+
D.1.14	++	＞+
			D.2	+++	+++
D.2.1	+++	++
			D.2.2	+++	＞+
D.2.3	+++	+++
			D.2.4	+++	+++
D.2.5	+++	++
			D.2.6	++	+
D.2.7	+++	+++
			D.2.8	++	+++
D.2.9	+++	+++
			D.2.10	+++	+++
D.3.1	+++	+++
			D.3.2	+++	+++
D.3.3	+++	++
			D.3.7	+++	+++
D.3.8	+++	+++
			D.3.11	+++	+++
D.3.12	+++	+++
			D.3.15	+++	+++
D.3.24	+++	+++
			D.3.26	+++	+++
D.3.27	+++	+++
			D.3.29	+++	+++
D.3.31	++	++
			D.3.32	+++	+++
D.3.34	+++	+++
			D.3.36	+++	+++
D.3.37	+++	+++
			D.3.38	+++	+++
D.3.39	+++	+++
			D.3.43	+++	+++
D.3.49	+++	++
			D.3.50	+++	+++
D.3.54	+++	+++
			D.3.55	+++	+++
D.3.57	+++	+++
			D.3.58	+++	+++

D.3.59	+++	++
			D.3.62	+++	+++
D.3.64	+++	+++
			D.3.66	+++	+++
D.3.67	+++	+++
			D.3.68	+++
D.3.69	+++
			D.3.70	+++	+++
D.3.73	+++	+++
			D.3.75	+++	+++
D.3.76	+++
			D.3.77	+++
D.3.78	+++
			D.3.80	+++
D.3.87	+++
			D.3.89	+++
D.3.91	+++	+++
			D.3.92	+++	+++
D.3.93	+++	+++
			D.3.94	+++	+++
D.3.96	+++	+++
			D.3.97	+++	+++
D.3.102	+++	++
			D.3.103	+++	++
D.3.104	+++	++
			D.3.105	+++	++
D.3.115	+++
			D.3.117	+++	+++
D.3.119	+++	+++
			D.3.122	+++	+++
D.3.124	+++	+++
			D.3.125	+++	+++
D.3.126	+++	+++
			D.3.128	+++	++
D.3.129	+++	+++
			D.3.130	+++
D.3.131	+++	+++
			D.3.132	+++	+++
D.3.133	+++	++
			D.3.136	+++	＞+
D.3.137	++	+
			D.3.138	++	++
D.3.161	+++	++
			D.3.174	++	+++

D.3.175	++	++
			D.3.176	+++	+++
D.3.177	+++	+++
			D.3.178	++	+++
D.3.179	+++	+++
			D.3.180	+++	+++
D.3.182	++	++
			D.3.185	+++	+++
D.3.186	+++	+++
			D.3.189	+++	+++
D.3.190	+++	+++
			D.3.191	+++	+++
D.3.192	++	+
			D.4.3	+++	+++
D.4.4	+++	+++
			D.4.6	++	+++
D.4.7	++	+++
			D.4.8	++	+++
D.4.9	++	+++
			D.6.3	+++	+++
D.6.5	+++	+++
			D.6.8	++	+++
D.6.9	+++	+++
			D.7.1	+++	+
D.7.2	+++	+
			D.7.3	+++	+
D.7.4	+++	＞+
			D.7.5	+-H-	++
D.7.6	+++	＞+
			D.7.7	+++	＞+
D.7.8	+++	＞+
			D.7.11	+++	+
D.7.12	+++	＞+
			D.7.17	+++	++
D.7.19	+++	+
			D.7.20	+++	+
D.7.21	+++	+
			D.7.23	+++	＞+
D.7.24	+++	++
			D.7.25	+++	+
D.7.26	+++	+
			D.7.27	+++	+
D.7.28	+++	＞+
			D.7.30	++	＞+

D.7.31	+++	＞+
			D.7.32	+++	+
D.7.33	+++	+
			D.7.35	+++	＞+
D.7.36	+++	+
			D.7.37	+++	＞+
D.7.38	+++	++
			D.7.39	+++	+
D.7.41	+++	+++
			D.7.60	+++	+
D.7.61	+++	＞+
			D.8	+++	+++
D.8.4	++	+++
			D.8.5	+++	+++
D.8.6	+++	+++
			D.8.18	++	++
D.8.19	+++	+++
			D.8.20	+++	+++
D.9	+++	+++
			D.12	+++	+++
D.16.6	+++	+++
			D.18	+++	+++
D.19	+++	+++
			D.24.3	+++	+++
D.24.4	+++	+++
			D.24.6	+++	+++
D.24.8	+++	+++
			D.24.9	+++	+++
D.24.10	+++	+++
			D.24.11	+++	+++
D.24.12	+++	+++
			D.24.14	+++	+++
D.24.15	+++	+++
			D.24.16	+++	+++
E.1.I	+++	＞+
			E.1.2	+++	+
E.1.3	+++	++
			E.1.4	+++	++
E.1.5	+++	＞+
			E.1.6	++	+
E.1.7	+++	+
			E.1.8	+++	＞+
E.1.10	+++
			E.1.11	+++	++

E.1.12	+++	＞+
			E.1.13	+++	+
E.1.14	+++
			E.1.15	+++	++
E.1.16	+++	+++
			E.1.17	+++	+++
E.1.18	+++	+++
			E.1.19	+++	++
E.1.20	+++	+++
			E.1.21	+++	+++
E.1.22	+++	＞+
			E.1.23	+++	+++
E.1.24	+++	+++
			E.1.25	+++	+++
E.1.26	+++	+++
			E.1.27	+++	+++
E.1.28	+++	++
			E.1.29	+++	++
E.1.30	+++	+
			E.2.1	+++	+++
E.2.2	+++	++
			E.2.3	+++	+
E.2.4	+++	＞+
			E.2.5	+++	+
E.2.6	+++	++
			E.2.7	+++	+
E.2.8	+++	+
			E.2.9	+++	++
E.2.10	+++	＞+
			E.2.11	+++	＞+
E.2.12	+++	+++
			E.2.13	+++	+
E.2.14	+++	＞+
			E.2.15	+++	＞+
E.2.16	+++	＞+
			E.2.18	+++	+
E.2.19	+++	+
			E.2.20	+++	+
E.2.21	+++	+
			E.2.22	+++	++
E.2.23	+++	++
			E.2.24	+++	＞+
E.2.25	+++	+
			E.2.26	+++	＞+

E.2.27	+++	＞+
			E.2.28	+++	＞+
E.2.29	+++	+
			E.2.31	+++	＞+
E.2.32	+++	＞+
			E.2.33	+++	+
E.2.34	+++	+
			E.2.35	+++	＞+
E.2.36	+++	＞+
			E.2.37	+++	＞+
E.2.38	+++	+
			E.2.39	+++	++
E.2.40	+++	+
			E.2.41	+++	＞+
E.2.42	+++	＞+
			E.2.45	+++	+++
E.2.46	+++	++
			E.2.47	+++	＞+
E.2.48	+++	++
			E.2.49	+++	＞+
E.2.50	+++	＞+
			E.2.51	++	＞+
E.2.52	+++	+
			E.2.53	++	＞+
E.2.54	+++	＞+
			E.2.55	+++	+
E.2.56	+++	+
			E.2.57	+++	+
E.2.58	+++	+
			E.2.59	+++	+
E.2.60	+++	+
			E.2.61	+++	+
E.2.62	+++	＞+
			E.2.64	+++	＞+
E.2.65	++	＞+
			E.2.66	+++	＞+
E.2.67	+++	+
			E.2.68	+++	＞+
E.2.69	+++	＞+
			E.2.70	+++	＞+
E.2.75	+++	＞+
			E.2.76	+++	+
E.2.77	+++	+
			E.2.78	+++	+

E.2.79	+++	++
			E.2.80	++	+
E.2.81	++	+
			E.3	+++	+++
E.3.1	+++	+++
			E.3.2	+++	+++
E.3.3	+++	+++
			E.3.4	++	+++
E.3.5	+++	+++
			E.3.6	+++	+++
E.3.7	+++	+++
			E.3.8	+++	+++
E.3.9	+++	+++
			E.3.10	+++	+++
E.4	+++	+++
			E.4.1	++	++
E.4.2	++	+++
			E.4.3	+++	+++
E.5	+++	+++
			E.5.1	+++	+++
E.5.2	+++	+++
			E.5.3	++	++
E.5.5	+++	+++
			E.5.6	+++	+++
E.5.7	+++	+++
			E.5.8	+++	+++
E.5.9	+++	+++
			E.5.10	+++	+++
E.5.11	+++	+++
			E.5.12	+++	+++
E.5.13	+++	+++
			E.5.16	+++	+++
E.5.17	+++	++
			E.5.18	+++	+++
E.5.19	+++	+++
			E.5.20	+++	+++
E.5.21	+++	+++
			E.5.22	+++	+++
E.5.24	+++	++
			E.5.25	+++	+++
E.5.26	+++	++
			E.5.27	+++	+++
E.5.28	+++	+++
			E.5.29	+++	+++

E.5.30	+++	++
			E.5.31	+++	+++
E.5.32	+++	+++
			E.5.33	+++	++
E.5.34	+++	+++
			E.5.35	+++	+++
E.5.36	++	++
			E.5.37	+++	+++
E.5.40	+++	+++
			E.5.41	++	+++
F.1	+++
			F.2.1	++	++

Pharmaceutical prepn and formulation

When the medicine, the form administration that the compound of general formula (I) can pharmaceutical composition.These compsns can the number of ways administration, comprises oral, rectum, in skin, subcutaneous, intravenously, intramuscular and nose, and can use the well-known mode of pharmaceutical field to prepare.

The present invention also comprises pharmaceutical composition, and it contains as one or more compounds of the above-mentioned general formula (I) of activeconstituents and one or more pharmaceutically useful carrier combinations.In preparation during compsn of the present invention, activeconstituents usually and mixed with excipients, by the vehicle dilution or for example be encapsulated within such carrier with the form of capsule, pouch, paper or other containers.When vehicle was used as thinner, it can be solid, semisolid or fluent material, as media, carrier or the medium of activeconstituents.Therefore; The form that compsn can be taked is tablet, pill, pulvis, lozenge, pouch; Cachet, elixir, outstanding agent, emulsion, solution, syrup, aerosol (as solid or in liquid medium); For example contain until the ointment of 10% weight active compound the powder of soft hard gelatin capsule, suppository, aseptic parenteral solution and sterile packed.

When the preparation preparation, active compound can be pulverized so that suitable particle size to be provided before making up with other compositions.If active compound is largely insoluble, it can be crushed to less than 200 purpose particle sizes.If active compound is water-soluble basically, particle size can be through pulverizing adjustment so that the distribution of basic homogeneous in the preparation to be provided, like about 40 orders.

The example of the vehicle that some are suitable comprises lactose, glucose, sucrose, Sorbitol Powder, mannitol, starch; Gum arabic, calcium phosphate, alginate, tragakanta, gelatin, Calucium Silicate powder; Microcrystalline Cellulose, Vinylpyrrolidone polymer, Mierocrystalline cellulose, water, syrup, and methylcellulose gum.Said preparation can also comprise lubricant, talcum for example, Magnesium Stearate, and MO; Wetting agent; Emulsifying agent and suspension agent; Sanitas, for example methyl and propyl hydroxy benzoic ether; Sweeting agent and seasonings.Compsn of the present invention can be through using methods known in the art, is made into preparation being administered into patient after, providing activeconstituents rapid, the lasting or release that delays.

Said compsn can be made into unit dosage, and each dosage contains from about 5 to about 100 milligrams, and more generally about 10 to about 30 milligrams said activeconstituents.Said term " unit dosage " refers to physically discrete unit, is suitable for people's object and other mammiferous single doses, and constituent parts contains the active substance through the predetermined amount that calculates the required result of treatment of generation, and suitable pharmaceutical excipient.

Active compound is effective in wide dosage range, and usually with the medicine effective quantity administration.Yet should be appreciated that the amount of the compound of actual administration confirms that according to relevant situation these situations comprise illness to be treated by the doctor usually; The route of administration of selecting; The compound of actual administration, the age of individual patient, body weight and reaction, severity of patient symptom or the like.

For example for the tablet, main activeconstituents mixes the solid preformulation composite that contains the uniform mixture of The compounds of this invention with formation with drug excipient for the preparation solids compsn.When being called equal phase time to these pre-preparation compositions, activeconstituents is evenly dispersed in whole compsn so that compsn usually can easily assign to same effective unit formulation for example in tablet, pill and the capsule again.This solid preformulation and then assign to contains in the unit dosage of the above-mentioned type of 0.1 to about 500mg activeconstituents of the present invention for example.

Tablet of the present invention or pill can be applied or be compound so that the formulation with prolongation effect advantage to be provided.For example, tablet or pill can comprise internal dose and outside dosage component, and the latter is the shell form on the former.These two components can be separated by enteric layers, and this layer is used for resisting the decomposition of stomach and allows internal composition intactly to get into duodenum or delay to discharge.Multiple material can be used to such enteric layers or coating, and such material comprises multiple polymers acid and polymeric acid and for example shellac, mixtures of material such as Tego Alkanol 16 and cellulose acetate.

Compound wherein of the present invention and compsn can be introduced into the liquid form that is used for oral or drug administration by injection and comprise the aqueous solution; The syrup that seasoning is suitable; Aqueous suspensions or oil suspension; With with edible oil for example Oleum Gossypii semen, til, Oleum Cocois or peanut oil, and the elixir and the similar emulsion of drug media seasoning.

The compsn that is used for sucking or be blown into comprises the solution and the suspension of pharmaceutically useful aqueous solvent or organic solvent or its mixture, and powder.The liquid or solid compsn can comprise above-mentioned suitable pharmaceutically useful vehicle.In some embodiments, compsn oral or nasal respiration path are used for part or whole body effect and administration.Compsn can utilize rare gas element and atomize.The solution of atomizing can directly suck from atomisation unit, and perhaps atomisation unit can be connected to face shield or intermittent positive pressure breathing (IPPB) machine.Solution, suspension, or powder composition is from send the device per os or the nose administration of said preparation in a suitable manner.

The amount that is administered into patient's compound or compsn will depend on the material of administration, and the purpose of administration is for example prevented or treated, patient's state, mode of administration or the like and changing.In therapeutic was used, compsn was with enough treatments or at least partly stop the symptom of disease and the amount of complication thereof to be administered into the patient who suffers from disease.Be enough to realize that the amount of this purpose is called " treatment significant quantity ".Effective dose will depend on the disease condition of being treated and the clinical nursing doctor severity according to disease, factor such as patient's age, body weight and overall state and judging.

The compsn that is administered into patient can be the form of pharmaceutical composition as stated.These compsns can pass through conventional Aseptic technique sterilization, or can sterile filtration.The aqueous solution can use by pack, or freeze-drying, and freeze-dried prepn mixes with aseptic aqueous carrier before administration.The pH of compound formulation usually between 3 to 11, more preferably from 5 to 9, and most preferably from 7 to 8.Should be appreciated that the use of above-mentioned vehicle, carrier or stablizer can cause forming drug salts.

The therapeutic dose of The compounds of this invention can according to for example should the treatment concrete purposes, the administering mode of compound, patient's healthy state, and the prescription doctor judgement and change.The ratio of The compounds of this invention or concentration will change with multiple factor in the pharmaceutical composition, comprise dosage, chemical property (like hydrophobicity), and route of administration.For example, The compounds of this invention can be provided in to contain about 0.1 and in the water-based physiological buffer of about 10%w/v compound, is used for parenterai administration.Some common dosage ranges be every day about 1 μ g/kg to about 1g/kg body weight.In some embodiments, dosage range from every day about 0.01mg/kg body weight to about 100mg/kg body weight.Dosage depends on such variable most probably, like the type and the progress degree of disease or imbalance, the overall health of given patient, the relative biological effectiveness of selected compound, the prescription of vehicle, and route of administration.Effective dose can be released from the dose response curve from external or animal model test macro.

The present invention also comprises the pharmaceutical kit that is effective to treat or prevent inflammatory diseases, and one or more container contains the pharmaceutical composition of the compound that comprises the general formula (I) of treating significant quantity.If desired, such test kit also comprises the conventional medicine reagent constituents that one or more are different, such as container with one or more pharmaceutically useful carriers, and other containers or the like, this is conspicuous to those skilled in the art.Can also in test kit, comprise, perhaps as inset or as the specification sheets of the demonstration administration group component of label, the guide of administration, and/or be used for the guide of blending ingredients.

Those, to various modifications that the present invention carry out is conspicuous according to foregoing description to those skilled in the art except that described herein.Such modification also drops in the scope of claim.Each reference that the application quotes comprises patent, the patented claim of announcement and journal of writings, at this with its hereby incorporated by reference.

Claims

1. the compound or pharmaceutically acceptable salt thereof of formula (I),

Wherein:

R ¹Be C ₁-C ₈Alkyl;

R ²Be-CH (R ⁷) ZR ⁸

R ⁷Be H or C ₁-C ₁₀Alkyl;

R ⁸Be H, C ₁-C ₁₀Alkyl, C ₁-C ₁₀Alkyl-S (=O) ₂-, C ₆-C ₁₈Aryl-S (O) ₂-, H ₂NS (=O) ₂-or-SO ₃H,

Z is O;

Q is-B (OH) ₂

X is R ^AC (=O)-;

R ^ABe C ₃-C ₂₀Assorted carbocylic radical, the optional replacement with 1-3 R ²¹

R ²¹Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₁₀Thiazolinyl, C ₂-C ₁₀Alkynyl ,-OR ^21a,-SR ^21a,-CN, halogen, halo C ₁-C ₁₀Alkyl ,-NH ₂,-NH (C ₁-C ₁₀Alkyl) ,-N (C ₁-C ₁₀Alkyl) ₂,-NHC (=O) O-C ₁-C ₁₀Alkyl ,-NHC (=O) C ₁-C ₁₀Alkyl ,-COOH ,-C (=O) O-C ₁-C ₁₀Alkyl ,-C (=O) C ₁-C ₁₀Alkyl ,-C (O) H ,-S (=O)-C ₁-C ₁₀Alkyl ,-S (=O) ₂-C ₁-C ₁₀Alkyl ,-S (=O)-C ₆-C ₁₈Aryl ,-S (=O) ₂-C ₆-C ₁₈Aryl, optional with 1-5 R ²²Substituted C ₃-C ₂₀Carbocylic radical, and optional with 1-5 R ²²Substituted C ₃-C ₂₀Assorted carbocylic radical;

R ^21aBe H, C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, C ₃-C ₂₀Carbocylic radical, or C ₃-C ₂₀Assorted carbocylic radical;

R ²²Be selected from:

C ₁-C ₁₀Alkyl, C ₂-C ₁₀Thiazolinyl, C ₂-C ₁₀Alkynyl, phenyl, halogen, halo C ₁-C ₁₀Alkyl, C ₁-C ₈Alkoxyl group, C ₁-C ₈Thio alkoxy, amino, C ₁-C ₁₀Alkylamino, two C ₁-C ₁₀Alkylamino, carboxyl, C ₁-C ₁₀Alkyl-OC (=O)-, C ₁-C ₁₀Alkyl-C (=O)-, C ₆-C ₁₈Aryl-OC (=O)-, C ₁-C ₁₀Alkyl-OC (=O) NH-, C ₆-C ₁₈Aryl-OC (=O) NH-, C ₁-C ₁₀Alkyl-C (=O) NH-, C ₁-C ₁₀Alkyl-C (=O) O-, (C ₁-C ₁₀Alkyl-O) _r-C ₁-C ₁₀Alkyl, HO-(C ₁-C ₁₀Alkyl-O) _r-C ₁-C ₁₀Alkyl-,-OH ,-SH ,-CN ,-N ₃,-CNO ,-CNS, C ₁-C ₁₀Alkyl-S (=O)-, C ₁-C ₁₀Alkyl-S (=O) ₂-, H ₂NS (=O)-, and H ₂NS (=O) ₂-; And

R is 1,2,3,4,5,6,7,8,9, or 10;

Each C wherein ₃-C ₂₀Assorted carbocylic radical is independently selected from: morpholinyl, and thio-morpholinyl, piperazinyl, tetrahydrofuran base, tetrahydro-thienyl, 2, the 3-dihydro benzo furyl, 1,3-benzo dioxole, phendioxin, the 4-diox, piperidyl, pyrrolidyl, different Oxazolidinyl, the isothiazole alkyl, pyrazolidyl,

Oxazolidinyl, thiazolidyl, imidazolidyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl; Furyl, quinolyl, isoquinolyl, thienyl, imidazolyl, thiazolyl, indyl, pyrryl oxazolyl, benzofuryl, benzothienyl, benzothiazolyl ， isoxazolyl, pyrazolyl, triazolyl, tetrazyl; Indazolyl, 1,2,4-thiadiazolyl group, isothiazolyl, purine radicals, carbazyl and benzimidazolyl-.

2. the compound of claim 1, wherein R ¹Be C ₁-C ₄Alkyl.

3. the compound of claim 1, wherein R ¹It is the 2-propyl group.

4. the compound of the formula of claim 1 (I), or its pharmacologically acceptable salt,

Wherein:

R ¹Be C ₁-C ₈Alkyl;

R ²Be-CH (R ⁷) ZR ⁸

R ⁷Be H or methyl;

R ⁸Be H, C ₁-C ₁₀Alkyl,

-S (=O) ₂-C ₁-C ₁₀Alkyl ,-S (O) ₂-C ₆-C ₁₈Aryl ,-S (=O) ₂-NH ₂Or-SO ₃H,

Z is O;

Q is-B (OH) ₂

X is R ^AC (=O)-;

R ²¹Be selected from:

C ₁-C ₂₀Alkyl, C ₂-C ₂₀Thiazolinyl, C ₂-C ₂₀Alkynyl, C ₁-C ₂₀Alkoxyl group, C ₁-C ₂₀Thio alkoxy ,-OH ,-CN, halogen, halo C ₁-C ₁₀Alkyl ,-NH ₂,-NH (C ₁-C ₁₀Alkyl) ,-N (C ₁-C ₁₀Alkyl) ₂,-NHC (=O) O-C ₁-C ₁₀Alkyl ,-NHC (=O) C ₁-C ₁₀Alkyl ,-C (=O) O-C ₁-C ₁₀Alkyl ,-C (=O) C ₁-C ₁₀Alkyl ,-S (=O)-C ₁-C ₁₀Alkyl ,-S (=O) ₂-C ₁-C ₁₀Alkyl ,-S (=O)-C ₆-C ₁₈Aryl ,-S (=O) ₂-C ₆-C ₁₈Aryl, optional with 1-5 R ²²Substituted C ₃-C ₂₀Carbocylic radical; And it is optional with 1-5 R ²²Substituted C ₃-C ₂₀Assorted carbocylic radical;

R ²²Be selected from:

R is 2,3,4,5,6,7,8,9, or 10;

Each C wherein ₃-C ₂₀Assorted carbocylic radical is independently selected from: morpholinyl, and thio-morpholinyl, piperazinyl, tetrahydrofuran base, tetrahydro-thienyl, 2, the 3-dihydro benzo furyl, 1,3-benzo dioxole, phendioxin, the 4-diox, piperidyl, pyrrolidyl, different

Oxazolidinyl, the isothiazole alkyl, pyrazolidyl, Oxazolidinyl, thiazolidyl, imidazolidyl, pyridyl, pyrimidyl, pyrazinyl, pyridazinyl, triazinyl; Furyl, quinolyl, isoquinolyl, thienyl, imidazolyl, thiazolyl, indyl, pyrryl oxazolyl, benzofuryl, benzothienyl, benzothiazolyl ， isoxazolyl, pyrazolyl, triazolyl, tetrazyl; Indazolyl, 1,2,4-thiadiazolyl group, isothiazolyl, purine radicals, carbazyl and benzimidazolyl-.

5. the compound of the formula of claim 1 (I), or its pharmacologically acceptable salt,

Wherein:

R ¹It is the 2-propyl group;

R ²Be-CH (CH ₃) OH;

Q is-B (OH) ₂

X is R ^AC (=O)-;

R ^ABe with 0-1 R ²¹Substituted pyrazinyl; With 0-1 R ²¹Substituted quinolyl; With 0-1 R ²¹Substituted imidazolyl; With 0-1 R ²¹Substituted tetrahydrofuran base; With 0-1 R ²¹Substituted oxo thiazolidyl; With 0-1 R ²¹Substituted benzothiazolyl; With 0-2 R ²¹Substituted thiazolyl; With 0-2 R ²¹Substituted furyl; With 0-1 R ²¹Substituted pyrrolidyl; With 0-1 R ²¹Substituted piperidyl; With 0-1 R ²¹Substituted piperazinyl; Or with 0-1 R ²¹Substituted pyridyl; With

R ²¹Be selected from:

6. compound or pharmaceutically acceptable salt thereof or free alkali form are selected from:

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-naphthalene-2-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 2-Zinamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-(1; 3-dioxy-1,3-dihydro-isoindole-2-yl)-propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-[(1; 1-dimethyl-oxyethyl group) carbonylamino] BM

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl-2-(2-methoxy ethoxy) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl-2-[2-(2-methoxy ethoxy) oxyethyl group] ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-3-(ethoxy carbonyl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-piperidines-1-base-ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(1-methyl-piperidin-4-yl)-yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-acetylaminohydroxyphenylarsonic acid ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(methoxycarbonyl) yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(1-butyl-piperidin-4-yl)-yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-butoxy ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-decyl amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-naphthalene-1-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 2-phenyl-acetamides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-1-phenyl cyclopentane formamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2R)-the 2-phenylbutanamides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2S)-the 2-phenylbutanamides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-lauramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-decoylamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-ethanamide

N-[(1S)-1-[[[(1R)-1-[[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(1; The 1-dimethyl ethyl) cyclohexane carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-anti--4-amyl group cyclohexane carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 4-phenylbutanamides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(3-p-methoxy-phenyl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S56S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(1, the 1-dimethyl ethyl) BM

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-pelargonamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(RS)-2-cyclopentyl hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-thiophene-2-carboxamide derivatives

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2, the 3-difluorobenzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl-2-(2-iodophenyl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-cyclohexane carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(4-bromophenyl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-BM

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 2-methyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 4-brombenzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2S)-the 2-Phenylpropionamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-2-methyl-3-phenyl-acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-[(naphthalene-2-yl) oxygen base] ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2, the 2-amide dimethyl butyrate

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(2-chloro-phenyl-) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-thiotolene-2-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-suitable-3-(2-p-methoxy-phenyl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2-methylphenoxy) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(2; The 5-3,5-dimethylphenyl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-anti--3-(2-bromophenyl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-isopropyl benzene methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(4-aminomethyl phenyl) yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(2-naphthyl sulfane base) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-methyl hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-thiophene-2-base-propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2; 4-dimethylthiazole-5-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-furans-3-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2R)-the 2-Phenylpropionamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-suberyl ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-1-methyl cyclopropane methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-1-methyl-cyclohexyl alkane methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-[(1S; 2R, 5S)-2-sec.-propyl-5-methylcyclohexyl] the oxygen yl acetamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-the 2-butylene acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-methylbutyryl amine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 3-Phenylpropionamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(4-p-methoxy-phenyl)-yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-thiophene-3-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl-2-thiene-3-yl--ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-penta-2,4-diolefinic acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(4-sec.-propyl phenoxy) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(4-ethyl phenoxy) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-the 2-methyl oneself-2-olefin(e) acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-(3-aminomethyl phenyl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-diamantane-1-yl acetamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl-(RS)-2-ring penta-2-thiazolinyl ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-diethyl amino yl-benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(RS)-2-methylbutyryl amine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-(4-aminomethyl phenyl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-oneself-2,4-diolefinic acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-pyrroles-1-base-BM

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-3-thiene-3-yl--acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the hept-2-ene" acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(3; The 4-dimethyl phenoxy) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-last of the ten Heavenly stems-9-alkene acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-11-2-olefin(e) acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-last of the ten Heavenly stems-3-olefin(e) acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2; 2-dimethyl--3-(2-methylpropenyl)-cyclopropane carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-methylcyclohexane methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-cyclohexyl valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-methoxyl group cyclohexane carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl-(3R)-3; 7-dimethyl--oct-6-ene acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-[(4-methyl-benzyl) sulfane base] propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(3S)-3; 7-dimethyl--oct-6-ene acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(RS)-4-ethyl decoylamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-fluoro-2-methoxy benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(4-bromine phenoxy)-ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(1-Methyl-1H-indole-3-yl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene 2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-six hydrogen-2; 5-methylene radical pentalene-3a (1H)-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-two ring [2.2.1] heptane-2-methane amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(RS)-2-(4-chloro-phenyl-) propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2S)-2-methylbutyryl amine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(4RS)-1-[(1; 1-dimethyl-oxyethyl group) carbonyl]-piperidines-4-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(RS)-4-methyl decoylamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-fluoro-5-methyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(two rings [2.2.1] heptan-2-yl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-cyclopropane carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 4-ethoxy benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3s2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-3-(4-bromophenyl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2S)-2-(6-methoxynaphthalene-2-yl)-propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-fluoro-4-methoxy benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-fluoro-3-methyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-ninth of the ten Heavenly Stems-2-olefin(e) acid acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-3-(naphthalene-2-yl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-quinoline-2-formamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-1-(4-p-methoxy-phenyl)-cyclopropane carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[methylene radical (nitro amino) methyl] amino] butyl]-the 3-crotonamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-myristamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-(1H-indol-3-yl)-propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-phenoxy yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-oxygen-5-phenyl-valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2RS)-1-((1; 1-dimethyl-oxyethyl group) carbonyl)-piperidines-2-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-pyridine-2-carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-pyridine-3-carboxamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-pyridine-4-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2S)-1-((1; 1-dimethyl-oxyethyl group) carbonyl)-piperidines-2-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2R)-1-((1; 1-dimethyl-oxyethyl group) carbonyl)-piperidines-2-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3,3-dimethyl--yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-[(phenyl amino) carbonyl] yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2,2-dimethyl-penten acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-thiophene-2-base-valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(3RS)-1-((1; 1-dimethyl-oxyethyl group) carbonyl)-piperidines-3-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl-8-phenyl-decoylamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-[[(1; 1-dimethyl-oxyethyl group) carbonyl] amino] propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-tridecanoyl amine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-succinic diamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-[[[(9H-fluorenes-9-yl) methoxyl group] carbonyl] amino] yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(dimethylamino) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-(4-fluorophenyl)-valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-8-oxygen-8-phenyl decoylamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(thiophene-2-yl) yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-oxygen-5-(thiophene-2-yl) valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(3-chloro-phenyl-) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-undecanoic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-heptyl benzene methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-6-phenyl hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-phenyl valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-10-hydroxyl decyl amide

N-[(1S)-1-[[[(1R)-1-[[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-5-oxygen-5-(4-phenylpiperazine-1-yl) valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3] 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(1H-tetrazolium-5-yl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(tetrazolium-1-yl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-(pyrimidine-2-base sulfane base) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-methyl sulfane base propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-(naphthalene-2-base sulfane base)-propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-[(phenyl methyl) sulfane base] ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-6-oxo heptamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-(4-methylsulfonyl phenyl)-4-oxo yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2S)-1-acetyl-pyrrole alkane-2-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-hydroxyl-2; 2-dimethyl propylene acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-ethyl sulfane yl acetamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-urea groups propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-methoxy propyl acid amides

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-methyl sulfane yl acetamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3H-imidazoles-4-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-7-oxygen-decoylamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-3-(imidazol-4 yl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(RS)-THF-3-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(E)-3-(2-p-methoxy-phenyl) acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-oxyethyl group ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-furans-2-base-propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3s2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(benzene sulfonyl) propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the sulphonamide yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(4S)-2-oxygen-1; 3-thiazolidine-4-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2R)-1-acetyl-pyrrole alkane-2-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-[(kharophen) methyl sulfane base]-propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(acetyl sulfane base) hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(thiophene-2-sulphonyl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(kharophen) yulocrotine

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2Z)-3-(propyl group aminocarboxyl)-2-acrylic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(octyl group sulphonyl) propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(octyl group sulfane base) propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-dimethyl-hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-hydroxyl hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the oxo valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the oxo hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-benzothiazole-6-methane amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(octyl group oxygen base) propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2-oxygen-tetramethyleneimine-1-yl)-ethanamide

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-BM,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-[2-(2-methoxy ethoxy) oxyethyl group] ethanamide

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-phenylbutanamides,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-(4-methylphenoxy) ethanamide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-hexanamide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-butyl benzamide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-naphthalene-2-methane amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(4-Methyl benzenesulfonyl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-heptamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-1-(formamyl) undecanoic amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(benzene sulfonyl) ethanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-naphthalene-1-sulphonamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-naphthalene-2-sulphonamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-last of the ten Heavenly stems-the 1-sulphonamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the Xin sulphonamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-benzsulfamide

N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl]-(2S)-4-[[imino-(nitro amino) methyl] amino]-2-[(2-naphthyl methyl)-amino]-valeramide

N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl]-(2S)-4-[[imino-(nitro amino) methyl] amino]-2-[(1-naphthyl methyl)-amino]-valeramide

N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl]-(2S)-4-[[imino-(nitro amino) methyl] amino]-2-[undecyl is amino]-valeramide

N-[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl]-(2S)-4-[[imino-(nitro amino) methyl] amino]-2-[(phenyl methyl) amino]-valeramide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-N '-(2-naphthyl) urea

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-N '-phenylurea

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-N '-heptyl urea

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-N '-(1-naphthyl) urea

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-N '-undecyl urea

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-N '-undecyl urea,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-N '-[5-(ethoxy carbonyl) amyl group] urea

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(2E)-and 3-(2-p-methoxy-phenyl)-1-oxo third-2-thiazolinyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((E)-2-methyl-3-phenyl acryloyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-(4-aminomethyl phenyl) butyryl radicals) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((2RS)-2-phenyl propionyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-(4-sec.-propyl phenoxy) acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-oxygen-5-phenyl pentanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(4RS)-and 1-[(1,1-dimethyl-oxyethyl group) carbonyl] piperidines-4-carbonyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-diethylamino benzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((E)-2-methyl oneself-2-enoyl-) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(thiophene-3-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-isopropyl benzene formyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-thiotolene-2-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(benzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((E)-2-butylene acyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((E)-penta-2,4-two enoyl-s) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3,3-dimethyl--butyryl radicals) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[5-(2, the 5-dimethyl phenoxy)-2,2-dimethyl-penten acyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2,2-dimethyl-penten acyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[4-(thiophene-2-yl) butyryl radicals] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[5-(4-fluorophenyl) pentanoyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2,2-dimethyl-caproyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(oneself-2,4-enoyl-) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[3-(thiophene-2-yl) acryl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-cyclohexyl pentanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((3R)-3,7-dimethyl-octa-6-enoyl-) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[3-[(4-methyl-benzyl) sulfane base] propionyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-pyrroles-1-base benzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-fluoro-2-methoxybenzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((2S)-2-methylbutyryl base) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(cyclopropane carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-phenetole formyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((E)-3-(4-bromophenyl) third-2-enoyl-) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(2S)-and 2-(6-methoxynaphthalene-2-yl)-propionyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[1-(4-p-methoxy-phenyl)-cyclopropane carbonyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-fluoro-4-methoxybenzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(E)-and 3-(naphthalene-2-yl) third-2-enoyl-] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-fluoro-3-methyl-benzyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[[[[(9H-fluorenes-9-yl) methoxyl group] carbonyl] amino] butyryl radicals] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-bromobenzene formyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-crotonoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(undecanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[4-(kharophen) butyryl radicals] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(6-phenyl caproyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-phenyl pentanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-methoxy propyl acyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2,2-dimethyl--3-(2-methylpropenyl)-cyclopropane carbonyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-methoxyl group hexanaphthene carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[3-(1H-indol-3-yl)-propionyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((RS)-2-ring penta-2-thiazolinyl-acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-thiophene-2-base-pentanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(6-oxygen-oenanthyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(7-oxygen-capryloyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(caproyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(oenanthyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-octyl group oxygen base-propionyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(benzothiazole-6-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(11-2-enoyl-) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(9-decenoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(myristoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-decyl amide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-(2S)-2-[(benzyloxycarbonyl) amino]-4-methylpent acid amides

1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] aminocarboxyl] propyl group]-10-(1,3-dioxy-1; 3-dihydro-isoindole-2-yl)-and capric acid-acid amides-N-[(1S), (2R)-the 2-hydroxyl

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(4-methyl benzoyl) amino] ethyl]-decyl amide,

N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-S-decanoyl amino-3-(caproyl is amino)-propionic acid amide,

N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-S-decanoyl amino-3-(4-fluorine sulfonamido) propionic acid amide,

N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-S-decanoyl amino-3-(3,4-Dimethoxyphenyl kharophen) propionic acid amide

N-[(1S)-1-[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-S-decanoyl amino-3-(phenyl urea groups) propionic acid amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-2-glycyl amine hydrochlorate

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the amino propionamide hydrochloride of 3-

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(4RS)-piperidines-4-carboxamide hydrochloride

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(RS)-piperidines-2-carboxamide hydrochloride

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2S)-piperidines-2-carboxamide hydrochloride

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-(2R)-piperidines-2-carboxamide hydrochloride

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(kharophen) ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(9-fluorenyl methyl oxygen base formamyl) ethyl]-decyl amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(amyl group-urea groups) ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(methanesulfonamido) ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(ethoxy carbonyl-succinyl-)-acid amides) ethyl]-decyl amide

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((2E)-3-ethoxy carbonyl-1-oxo third-2-thiazolinyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-pyrazine carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-butylbenzene-formyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-naphthoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[(3-(1,3-dihydro-1,3-dioxy-2H-isoindole-2-yl)-1-oxopropyl is amino)-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(2-methoxy ethoxy) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-the borate hydrochlorate,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-butoxy acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-[2-(2-methoxy ethoxy) oxyethyl group] acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(kharophen) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-the borate hydrochlorate,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[4-(methoxycarbonyl) butyryl radicals] amino]-l-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-(naphthalene-2-base oxygen base) acetyl) amino]-1-oxo amyl group) amino)-the 3-methylbutyl)-boric acid

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-thiophene-2-base-propionyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[2-(2-chloro-phenyl-) acetyl] amino]-the 3-methylbutyl]-the borate hydrochlorate,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(1-oxygen-4-(1-butyl piperidine-4-yl) butyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(the hot sulphonyl of 1-) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-the borate hydrochlorate,

[(1R)-1-[[(2S)-and 3-[(4-methyl benzoyl) amino]-2-[(decanoyl is amino)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(decanoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[[10-(1,3-dioxy-1,3-dihydro-isoindole-2-yl)-decanoyl] amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(1-oxo decyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(capryloyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(1-benzyl ring pentane carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((2R)-2-phenyl butyryl radicals) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[4-(1, the 1-dimethyl ethyl) hexanaphthene carbonyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(anti--4-amyl group hexanaphthene carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-phenyl butyryl radicals) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-(1, the 1-dimethyl ethyl) benzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(nonanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-thiophene carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2,3-two fluorobenzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(dodecanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(2-iodophenyl) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(hexanaphthene carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-methyl benzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((2S)-2-phenyl propionyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2,2-dimethyl butyrate acyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(quinoline-2-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[(ninth of the ten Heavenly Stems-the 2-enoyl-) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-methyl cyclohexane alkyl carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(hept-2-ene" acyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(3, the 4-dimethyl phenoxy) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((RS)-4-ethyl capryloyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(six hydrogen-2,5-methylene radical pentalene-3a (1H)-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(two ring [2.2.1] heptane-2-carbonyls) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-methyl caproyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2,4-dimethylthiazole-5-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(furans-3-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-suberyl acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(1-methyl cyclopropane carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-methylbutyryl base) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-phenyl propionyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(E)-and 3-(3-aminomethyl phenyl) acryl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-diamantane-1-base acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((RS)-2-methylbutyryl base) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-phenyl acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(4-p-methoxy-phenyl) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(4-bromophenyl) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((RS)-4-methyl capryloyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-fluoro-5-methyl benzoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[2-(and two the ring [2.2.1] heptan-the 2-yl) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(4-phenoxy butyryl radicals) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-pyridine carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-pyridine carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(tridecanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(8-phenyl capryloyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[4-(4-methylsulfonyl phenyl)-4-oxobutanoyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[3-(naphthalene-2-base sulfane base)-propionyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-[(phenyl methyl) sulfane base] acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(3-methyl sulfane base propionyl group) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[((2S)-1-acetyl-pyrrole alkane-2-carbonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[anti--3-(2-bromophenyl) acryl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(tetrazolium-1-yl) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(pyrimidine-2-base sulfane base) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(4-ethyl phenoxy) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(2, the 5-3,5-dimethylphenyl) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(8-oxygen-8-phenyl capryloyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(2-naphthyl sulfane base) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(RS)-and 2-cyclopentyl caproyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[3-(4-aminomethyl phenyl) acryl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[4-(4-p-methoxy-phenyl)-butyryl radicals] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-thiene-3-yl--acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[2-(dimethylamino) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[5-oxygen-5-(thiene-3-yl-) pentanoyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-ethyl sulfane base acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(10-hydroxy decanoyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(2-methyl sulfane base acetyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[(thiophene-2-sulphonyl) acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[3-(benzene sulfonyl) propionyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(RS)-and THF-3-carbonyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(naphthalene-1-sulphonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(naphthalene-2-sulphonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(benzenesulfonyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

N-[(1S)-1-[[[(1R)-1-[(4R, 5R)-4,5-dicyclohexyl-[1,3,2] dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-decyl amide,

N-[(1S)-1-[[[(1R)-and 1-[13,15-dioxy-14-boron-two spiral shell [5.0.5.3]-pentadecane-14-yl]-3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl]-amino] butyl]-the 4-phenylbutanamides.

7. compound or pharmaceutically acceptable salt thereof or free alkali form are selected from:

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[imino-(nitro amino) methyl] amino] butyl-2-[2-(2-methoxy ethoxy) kharophen] ethanamide

N-[1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl] methyl]-decyl amide,

N-[1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl] methyl]-2-[2-(2-methoxy ethoxy) oxyethyl group] ethanamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-5-urea groups amyl group]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-5-urea groups amyl group]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S; 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4; 6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-[4-(2-propyl group) phenyl] propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-3-[4-(ethyl) phenyl] propionic acid amide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-the 6-hydroxyl hexanamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-butyl phenyl ether sulphonamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-butyl-benzsulfamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[[imino-(nitro amino) methyl] amino] butyl]-4-amyl group-benzsulfamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[imino-(nitro amino) methyl] amino] butyl]-N '-(4-butyl phenyl) urea

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-4-[imino-(nitro amino) methyl] amino] butyl]-N '-(4-heptyl oxygen base phenyl) urea

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-4-(pyridin-3-yl) BM,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3:, 2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-the 2-Zinamide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-tridecanoyl amine,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-the 4-phenylbenzamaide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-2,2-dimethyl-decyl amide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-(4-phenoxy) BM,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-5-butyl-2-pyridine carboxamide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-4-propoxy-BM,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-3-(3-pyridyl) BM,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-6-phenyl-2-pyridine carboxamide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-3-propoxy-BM,

N-[(1S, 2R)-1-[[[(1R)-1-(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-1-bromonaphthalene-2-methane amide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene 1-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-6-bromonaphthalene-2-methane amide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-the 3-phenylbenzamaide,

N-[(1S, 2R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-4-(2-fluorophenyl) BM,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-formamyl ethyl]-the 2-Zinamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-formamyl ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-formamyl ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(benzyloxycarbonyl acid amides) ethyl]-4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-(1H-pyrazoles) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(benzyloxycarbonyl acid amides) ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(benzyloxycarbonyl acid amides) ethyl]-4-phenoxy benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(amino-ethyl)-4-butyl benzamide hydrochloride,

2-S-(4-butylbenzene-formamido group)-3-(2-pyrazinyl carbonylamino)-N-[(1S)-1-[[(1R)-and 1-(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[4-fluoro-benzsulfamide] ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(2,5-dimethyl--2H-pyrazoles) carbonylamino] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-(4-aminomethyl phenyl urea groups sulfonamido) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(3-phenyl-urea groups) ethyl]-the 4-phenoxy benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-(4-aminomethyl phenyl sulfonylurea group) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[4-fluoro-benzsulfamide] ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(4-sulfonamido phenyl) carbonyl amido] ethyl]-decyl amide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-(kharophen) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-y 1-]-the 3-methylbutyl] amino] carbonyl]-2-(methanesulfonamido) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-(propyl group urea groups) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(4-aminomethyl phenyl) carbonylamino] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(1,1-dimethyl-ethoxy carbonyl) amino] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(thiophene-2-base carbonyl) amino] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(thiophene-2-base carbonyl) amino] ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(caproyl is amino) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-and 1-[3aS, aS, 6S, 7aR]-six hydrogen-3a, 5,5-trimethylammonium-4, the 6-methyl isophthalic acid, 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-(cyclopropane carbonyl is amino) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(3-phenyl-urea groups) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(N-methyl-2-pyrryl carbonyl acid amides) ethyl]-4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[3aS, aS, 6S, 7aR]-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(3, the 4-Dimethoxyphenyl) kharophen] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(nicotinoyl is amino) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[3aS, aS, 6S, 7aR]-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(4-sulfonamido) benzamido-] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[3aS, aS, 6S, 7aR]-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(1H-tetrazolium-5-base-kharophen) ethyl]-4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(4-sulfonyloxy methyl phenyl) carbonylamino] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(nicotinoyl is amino) ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(4-(2H-tetrazolium-5-yl) phenyl) carbonylamino] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS; AS, 6S, 7aR)-six hydrogen-3a; 5; 5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(1-different

azoles-5-yl)-carbonylamino] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(4-cyano-phenyl) sulfonamido] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(1-methyl isophthalic acid H-imidazoles-4-) sulfonamido] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(2-thiophene) sulfonamido] ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(6-morpholine-4-nicotinoyl is amino) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(2-pyridine-4-thiazole carbonylamino) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(4-aminomethyl phenyl urea groups sulfonamido) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[4-fluoro-benzsulfamide] ethyl]-the 4-phenoxy benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1,3; 2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-[(2,5-dimethyl--2H-pyrazoles) carbonylamino] ethyl]-the 4-phenoxy benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(4-phenyl benzamido-) ethyl]-the 4-phenoxy benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(4-phenyl benzamido-) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(3-phenyl propiolyl is amino) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(2-hydroxyl-3-nicotinoyl is amino) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(the D-pyroglutamyl is amino) ethyl]-the 4-butyl benzamide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-(1-methylsulfonyl-piperidines-4-carbonylamino) ethyl]-the 4-butyl benzamide

N-[(1S)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(3-phenyl-urea groups) ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-(kharophen) ethyl]-decyl amide,

N-[(1S)-1-[[[(1R)-1-[(3aS, aS, 6S, 7aR)-and six hydrogen-3a, 5,5-trimethylammonium-4,6-methylene radical-1,3,2-benzo dioxo bora pentamethylene-2-base-]-the 3-methylbutyl] amino] carbonyl]-2-is amino] ethyl]-the decyl amide hydrochloride,

N-[(1R)-1-[[[(1R)-1-[(3aS, 4S, 6S, 7aR)-six hydrogen-3a; 5,5-trimethylammonium-4,6-methylene radical-1; 3,2-benzo dioxo bora pentamethylene-2-yl]-the 3-methylbutyl] amino] carbonyl]-2-[(4-methyl benzoyl) amino] ethyl]-the 4-butyl benzamide

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(4-phenyl butyryl radicals) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(undecyl aminocarboxyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(1-bromo-2-naphthoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(6-bromo-2-naphthoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-formamyl-2-[(decanoyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-formamyl-2-[4-butyl (benzoyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 2-[(decanoyl) amino]-1-oxygen-5-urea groups-amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 2-[(4-butylbenzene-formyl) amino]-1-oxygen-5-urea groups-amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(RS)-and 2-(4-chloro-phenyl-) propionyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[2-(4-) bromine phenoxy] acetyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[[3-(4-ethylphenyl) propionyl group] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[3-[4-heptyl oxygen base] phenyl]-urea groups]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 5-[[imino-(nitro amino) methyl] amino]-2-[(5-oxo caproyl) amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-5-[[imino-(nitro amino) methyl] amino]-2-[[(2RS)-and 1-[(1,1-dimethyl-oxyethyl group) carbonyl] piperidines-2-carbonyl] amino]-1-oxo amyl group] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(2-naphthoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(p-tolyl oxygen yl acetamide)-1-oxo butyl] amino]]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(tridecanoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(naphthalene-2-sulphonyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(4-phenyl benzoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(2,2 dimethyl--decanoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(4-phenoxy benzoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[[4-(1-propoxy-) butylbenzene-formyl] amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(3-pyridin-3-yl-) benzoyl-] amino]-1-oxo butyl] amino]-the 3-methylbutyl]-the borate hydrochlorate,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(3-propoxy--benzoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(3-phenyl benzoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(4-(2-fluorophenyl) benzoyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[[4-(3-pyridyl) benzoyl] amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(2-pyrazine carbonyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(5-butyl-pyridine-2-carbonyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(6-phenyl-pyridine-2-carbonyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(2-pyrazine carbonylamino)-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(kharophen)-2-[(decanoyl is amino)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(propyl group urea groups)-2-[(4-butyl)-benzamido-]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(methylsulfonyl amido)-2-[(4-butyl)-benzamido-]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-[2-(1H-pyrazoles) ethyl]-2-[(4-butyl)-] benzamido-]-the 1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-[(carbobenzoxy is amino)-2-[(4-butylbenzene-formamido group)]-1-oxopropyl]]]] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[(thiophene-2-base carbonyl) amino]-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-(kharophen)-2-[4-butyl-benzamido-]]-the 1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-[(thiophene-2-base carbonyl) amino]]-2-[(decanoyl is amino)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(caproyl is amino)-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[4-fluoro-benzsulfamide]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-[4-fluoro-benzsulfamide]-2-(decanoyl) amino]-the 1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(caproyl is amino)-2-[(decanoyl is amino)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(caproyl is amino)-2-[(cyclopropane carbonyl is amino)]-1-oxopropyl] amino]-the 3-methylbutyl] the 3-methylbutyl] amino] carbonyl]-2-(cyclopropane carbonyl is amino) ethyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[(3, the 4-Dimethoxyphenyl) kharophen]-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[1-N-methyl-2-pyrryl carbonylamino]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[4-sulphonamide benzamido-]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(nicotinoyl is amino)-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(3-phenyl urea groups)-2-(4-butylbenzene-formamido group)-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[(4-sulfonyloxy methyl) benzamido-]-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(3-phenyl urea groups)-2-(decanoyl is amino)-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(nicotinoyl is amino)-2-(decanoyl is amino)-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2R)-and 3-(4-aminomethyl phenyl carbonyl)-2-(decanoyl is amino)-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-[4-(1H-tetrazyl)-phenylcarbonyl group is amino]-2-(4-butylbenzene-formamido group)]-the 1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(2-different azoles base carbonylamino)-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid

[(1R)-1-[[(2S)-and 3-[1-methyl isophthalic acid H-imidazoles-4-sulphonamide]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[6-morpholine-4-base-pyridine-3-sulphonamide]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl] hydrochloride-boric acid,

[(1R)-1-[[(2S)-and 3-(6-morpholinyl vitamin PP)-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-(4-(1,3-dimethyl--1H-pyrazoles-5-carbonylamino)-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl) amino]-the 3-methylbutyl] hydrochloride-boric acid,

[(1R)-1-[[(2S)-and 3-[4-fluoro-benzsulfamide]-2-[(4-phenoxy benzoyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-(4-(1,3-dimethyl--1H-pyrazoles-5-carbonylamino)-2-[(4-phenoxy benzoyl) amino]-1-oxopropyl) amino]-the 3-methylbutyl] carbonylamino] ethyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(4-phenyl urea groups)-2-[(4-phenoxy benzoyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(4-phenylbenzamaide)-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(4-phenylbenzamaide)-2-[(4-phenoxy benzoyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-(Phenylpropionamide))]]]]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl]]] amino]]]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-(4-aminomethyl phenyl sulphonyl)-urea groups]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(4-(2-(4-pyridyl)-1,3-thiazoles-4-carbonylamino))-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-(1-methylsulfonyl piperidines-4-carbonylamino)-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-[(2-thiophene) sulfonamido]-2-[(4-butylbenzene-formamido group)]-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-3-(4-(1H-1,2,4-triazol-1-yl) benzoyl acid amides)]-2-[(4-butylbenzene-formyl) amino]-1-oxopropyl] amino]-the 3-methylbutyl] hydrochloride-boric acid,

[(1R)-1-[[(2S)-and 3-(4-phenyl urea groups)-2-(decanoyl is amino)-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

[(1R)-1-[[(2S)-and 3-acetylaminohydroxyphenylarsonic acid 2-decanoyl amino-1-oxopropyl] amino]-the 3-methylbutyl]-boric acid,

N-[(1S, 2R)-1-[[[(1R)-and 1-[13,15-dioxy-14-boron-two spiral shell [5.0.5.3] pentadecane-14-yl]-3-methylbutyl] amino] carbonyl]-the 2-hydroxypropyl]-the 4-butyl benzamide.

8. compsn, it is made up of each compound and pharmaceutically acceptable carrier of claim 1-7.

9. each compound of claim 1-7 is used for the application of the medicine of vitro inhibition proteasome activity in preparation.

10. each compound of the claim 1-7 of treatment significant quantity is in the application of the medicine of preparation through the Mammals administration that has or tend to have cancer being used for treat cancer.

11. the application of claim 10, wherein said cancer is selected from skin carcinoma, prostate cancer, colorectal carcinoma, carcinoma of the pancreas, kidney, ovarian cancer, mammary cancer, liver cancer, tongue cancer, lung cancer and smooth muscle tissue's cancer.

12. the application of claim 10, wherein said cancer is selected from white blood disease, lymphoma, non--He Jiejin lymphomas, myelomatosis, and multiple myeloma.

13. each compound of claim 1-7 is used for the application of the medicine of vitro inhibition proteolytic degradation in preparation.

14. the application of claim 13, wherein said protein labeling has ubiquitin.

15. the application of claim 13, wherein said albumen is p53.

16. each compound of the claim 1-7 of treatment significant quantity in preparation through quickening or the proteoclastic Mammals administration of enhanced is used for treating and quickens or the application of the proteoclastic medicine of enhanced to having or tending to have.

17. each compound of claim 1-7 in preparation through each compound of the suppressor factor I κ B and claim 1-7 of transcription factor NF-KB is contacted the application that is used for suppressing the active medicine of transcription factor NF-KB.

18. each compound of the claim 1-7 of treatment significant quantity is in the application of the medicine of preparation through the Mammals administration that has or tend to have the disease that is selected from the imbalance of human immune deficiency infections or inflammatory or imbalance being used for treat said disease or imbalance, said inflammatory imbalance is derived from transplant rejection, sacroiliitis; Infect inflammatory bowel, asthma; Osteoporosis; Osteo-arthritis, psoriasis, restenosis and autoimmune disease.

19. prepare the method for formula (II) compound,

Wherein:

D is a disappearance, O, S, NR ¹⁶, or CR ^15eR ^15f

R ^15a, R ^15b, R ^15c, R ^15d, R ^15e, R ^15fBe H independently of one another, C ₁-C ₁₀Alkyl, C ₃-C ₇Naphthenic base, C ₆-C ₁₈Aryl or C ₃-C ₂₀Heteroaryl, wherein said C ₁-C ₁₀Alkyl, C ₃-C ₁₀Naphthenic base, C ₆-C ₁₈Aryl or C ₃-C ₂₀Heteroaryl is optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, C ₁-C ₁₀Alkylamino, two C ₁-C ₁₀Alkylamino, C ₆-C ₁₈Aryl, or C ₃-C ₂₀Heteroaryl replaces;

Perhaps, R ^I5aAnd R ^15bThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base or 3-10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, C ₁-C ₁₀Alkylamino, two C ₁-C ₁₀Alkylamino, C ₆-C ₁₈Aryl, or C ₃-C ₂₀Heteroaryl replaces;

Perhaps, R ^15cAnd R ^15dThe C atom that connects with them forms C ₃-C ₁₀Naphthenic base or 3-10 element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, C ₁-C ₁₀Alkylamino, two C ₁-C ₁₀Alkylamino, C ₆-C ₁₈Aryl, or C ₃-C ₂₀Heteroaryl replaces;

Perhaps, R ^15bAnd R ^15cThe C atom that connects with them forms C with insertion D part ₆-C ₁₈Aryl, C ₃-C ₂₀Heteroaryl, C ₃-C ₁₀Naphthenic base or 3-10-element heterocycle alkyl, optional respectively by 1,2,3 or 4 halogens, C ₁-C ₄Alkyl, C ₁-C ₄Alkoxyl group, C ₁-C ₄Halogenated alkoxy, OH, amino, C ₁-C ₁₀Alkylamino, two C ₁-C ₁₀Alkylamino, C ₆-C ₁₈Aryl, or C ₃-C ₂₀Heteroaryl replaces;

R ¹⁶Be H or C ₁-C ₆Alkyl; With

P and q are respectively 1,2 or 3 independently;

Comprise a) glycol with formula (II-b):

Suitable tri-alkoxy borine with formula (II-a):

Under the condition that is suitable for the formula that forms (II-c) midbody, react for some time:

And b) with formula (II-c) midbody or and i) formula R ¹CH ₂MX ^HalReagent, wherein M is Mg or Li and X ^HalBe halogen, or with ii) formula R ¹CH ₂The reagent of Li reacts for some time under the condition that is suitable for the formula that forms (II) compound.

20. the method for claim 19, wherein R ¹⁷Be C ₁-C ₄Alkyl.

21. the method for claim 19, wherein R ¹⁷It is sec.-propyl.

22. the method for claim 19, the glycol of its Chinese style (II-b) is a pinine glycol, tetramethyl ethylene ketone, 1,1, ammediol; 1,2-Ucar 35,2,3-butyleneglycol, 1,1,2; The 2-tetramethylethylene glycol, 1,2-di-isopropyl terepthaloyl moietie, 5,6-decanediol, 1,2-dicyclohexyl terepthaloyl moietie; Dicyclohexyl-1,1 '-glycol, diethylolamine, or 1,2-xenyl-1.

23. the method for claim 19, the glycol of its Chinese style (II-b) is a pinine glycol.

24. the method for claim 19, wherein R ¹CH ₂MX ^HalBe R ¹CH ₂MgBr.

25. the method for claim 19, wherein R ¹It is sec.-propyl.

26. the method for claim 19 is used for preparation formula (II-i) compound:

Comprise

27. the compound of formula (II-ii):

28. a compound, its be [(1R)-1-[[(2S, 3R)-3-hydroxyl-2-[(6-phenyl-pyridine-2-carbonyl) amino]-1-oxo butyl] amino]-the 3-methylbutyl]-boric acid or its pharmacologically acceptable salt.