CN104086503B - PAR-1 antagonist and uses thereof - Google Patents
PAR-1 antagonist and uses thereof Download PDFInfo
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- CN104086503B CN104086503B CN201410352040.2A CN201410352040A CN104086503B CN 104086503 B CN104086503 B CN 104086503B CN 201410352040 A CN201410352040 A CN 201410352040A CN 104086503 B CN104086503 B CN 104086503B
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- antagonist
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- FGKWENZUQLBACU-UHFFFAOYSA-N CCOc(c(N1CCOCC1)c1)c(C(C)(C)C)cc1C(CBr)=O Chemical compound CCOc(c(N1CCOCC1)c1)c(C(C)(C)C)cc1C(CBr)=O FGKWENZUQLBACU-UHFFFAOYSA-N 0.000 description 1
- NHYBDYVOBILTQO-UHFFFAOYSA-N CCOc(c(N1CCOCC1)c1)c(C(C)(C)C)cc1C(C[n]1nnc(-c(cc2)c(C)c(OC)c2OC)n1)=O Chemical compound CCOc(c(N1CCOCC1)c1)c(C(C)(C)C)cc1C(C[n]1nnc(-c(cc2)c(C)c(OC)c2OC)n1)=O NHYBDYVOBILTQO-UHFFFAOYSA-N 0.000 description 1
- NHMNQPYTKXTHQW-UHFFFAOYSA-N Cc(c(-c1n[nH]nn1)ccc1OC)c1OC Chemical compound Cc(c(-c1n[nH]nn1)ccc1OC)c1OC NHMNQPYTKXTHQW-UHFFFAOYSA-N 0.000 description 1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
The present invention relates to the pharmaceutical field relevant to thrombotic diseases.Specifically, the present invention has the PAR-1 antagonist of following formula brand new, for oxyethyl group replaces on its N-morpholinyl side phenyl ring, for bi-methoxy replaces on opposite side phenyl ring.And it treats the purposes in thrombotic diseases medicine in preparation.
Description
Technical field
The present invention relates to the pharmaceutical field relevant to thrombus disease.Specifically, the present invention relates to PAR-1 antagonist of the medicative a kind of brand new of thrombotic diseases and preparation method thereof, and containing its pharmaceutical composition.
Background technology
Proteinase activated receptors 1 (Protease Activated Acceptor-1, PAR-1) is the novel targets of the antiplatelet class antithrombotic reagent found recently.Proteinase activated receptors 1 is thrombin receptor again, zymoplasm by coagulation cascade activate after by PAR-1 receptor acting in thrombocyte thus activate thrombocyte, cause platelet aggregation thus cause thrombus and blood coagulation.Being rich in platelet component in the thrombus that PAR-1 causes, is the main reason of arterial thrombus.PAR-1 antagonist can block thrombin activation thrombocyte, thus interruption artery thrombosis, may be used for treatment acute coronary artery disease (Acute Coronary Syndrome).Several PAR-1 inhibitor has been had to be in clinical study (ChackalamannilS., Thrombin Receptor (Protease Activated Receptor-1) Antagonists as PotentAntithrombotic Agents with Strong Antiplatelet Effects, J.Med.Chem., 2006,49 (18), 5389-5403).
Traditional is divided three classes for the medicine preventing and treating thrombotic diseases.The first kind is anticoagulation class, be divided into direct thrombin inhibitor and indirect thrombin inhibitors, such medicine carrys out inhibition thrombosis by the different links acting on coagulation cascade, has and suppresses various thrombotic effect, as vitamin K antagon and Xa factor inhibitor etc.; Equations of The Second Kind is antiplatelet class, and as COX-1 inhibitor and adp receptor antagonist etc., such medicine is mainly used in preventing and treating arterial thrombus; 3rd class is fibrinolytic agent, is mainly used in the scleroproein formed in lysed blood.
Mostly antiplatelet drug is traditional arterial thrombus protective agents, as clopidogrel and acetylsalicylic acid etc.The shortcoming of these medicines is that bleeding risk is larger.And as the PAR-1 antagonist of newfound antiplatelet class antithrombotic reagent, then there is less bleeding risk, therefore this compounds can as the very promising medicine for the treatment of arterial thrombus.
The invention discloses a kind of PAR-1 antagonist of tetrazole methyl phenyl ketone structure, for oxyethyl group replaces on its N-morpholinyl side phenyl ring, for bi-methoxy replaces on opposite side phenyl ring.May be used for the medicine preparing anti-arterial thrombus disease.
Summary of the invention
An object of the present invention is to provide a kind of there is good anti-thrombosis activity the compound with formula I structure and pharmaceutically acceptable salt.
Another object of the present invention be to provide preparation have formula I structure=compound and the method for pharmaceutically acceptable salt.
Another object of the present invention be to provide containing formula I structure and pharmaceutically acceptable salt as effective constituent, and the medicinal compositions of one or more pharmaceutically acceptable carrier, vehicle or thinners, and the application in treatment arterial thrombus.
Now in conjunction with object of the present invention, content of the present invention is specifically described.
The present invention has the compound of formula I structure:
Formula I of the present invention is synthesized by following steps:
Compound II per and compound III are reacted under the catalysis of acid or alkali, obtain compound (I).
The pharmacy acceptable salt of formula I of the present invention, include, but are not limited to the salt formed with various mineral acid example hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, Hydrogen bromide etc., also comprise the salt formed as acetic acid, succsinic acid, toxilic acid, oxysuccinic acid and each seed amino acid etc. with various organic acid.
The compound of formula I structure of the present invention has the antagonistic action of PAR-1, can be used as the medicine of effective constituent for the preparation of antithrombotic aspect.The activity of the compound of formula I structure of the present invention is verified by external model.
The compound of formula I structure of the present invention is effective in quite wide dosage range.The dosage that such as every day takes, within the scope of 1mg-500mg/ people, is divided into once or administration for several times.The actual dosage taking the compound of formula I structure can be decided according to relevant situation by doctor.These situations comprise: the physical state of patient, route of administration, age, body weight, individual reaction to medicine, the severity etc. of symptom.
Embodiment
Below in conjunction with embodiment, the present invention is further illustrated.It should be noted that, following embodiment be only for illustration of, and not for limiting the present invention.The various changes that those skilled in the art's training centre according to the present invention is made all should within the protection domain required by the application's claim.
Embodiment 1
Reaction raw materials: self-control, ordinary method.
2.40g (10mmol) Compound II per, 3.70g (10mmol) compound III and 4.15g (30mmol) solid carbonic acid potassium stir and spend the night in 20mL acetonitrile, then temperature rising reflux 3 hours.
Be poured into after reaction mixture is slightly cold in 200mL frozen water, stir, regulate pH=4 with concentrated hydrochloric acid, the dichloromethane extraction of 50mL × 3, merge organic phase, brine It, anhydrous sodium sulfate drying, boil off solvent on a rotary evaporator, the resistates obtained, through column chromatography purification, obtains sterling I, micro-yellow solid, MS, m/z=567 ([M+Na]
+).
Embodiment 2 extracorporeal platelet aggregation inhibition test
In 96 orifice plates, the platelet aggregation of inducing at TRAP (Glycoprotein) concentrates the pharmacology test carrying out material.The sodium citrate solution of 3.13% is added in advance in syringe, then the blood of suction 20mL healthy volunteer, under 1500g centrifugal 20 minutes, separate being rich in hematoblastic blood plasma (PRP) and processing with the amount of 1 μ L PGE1 solution (ethanolic solns of 500 μ g/mL)/mL PRP.After at room temperature hatching 5 minutes, by its under 1200g centrifugal 20 minutes with except leucocyte-removing.To not transfer in the PP pipe of 15mL with 5mL/ part containing leukocytic PRP in batches, and centrifugally under 3600g make pellet platelets.Then, drain upper plasma, the pellet platelets deriving from 5mL PRP is suspended in again 1mL Tyrode (120mM NaCl, 2.6mM KCl, 12mM NaHCO3,0.39mM NaH2PO4,10mM HEPES, 0.35%BSA, 5.5mM glucose, pH=7.4) in, and the platelet count of 3 × 105/ μ L is adjusted to Tyrode.By the 10mM CaCl2 solution-treated of this for 13mL cell suspension with 866 μ L, be drawn in 96 orifice plates with the amount of every hole 120 μ L, in the hole of 96 orifice plates, added 15 μ L material to be tested in advance.At room temperature hatch 30 minutes in dark, add 15 μ L TRAP solution (70-100 μM) as agonist, vibrate 20 minutes at 37 DEG C in SpectraMax, kinetics is noted down under 650nm, calculate the area under curve of negative control (tyrode/DMSO) and positive control (15 μ L agonist/DMSO), and difference is decided to be 100%.Aspirated with the form of serial dilution thing by compound to be tested, measure in duplicate, the same AUC measuring each material concentration, the AUC calculated compared with the control suppresses %.IC50 value is calculated according to 4 parametric equations by nonlinear regression analysis by this suppression %.Following table gives result:
| Sample | The suppression IC of platelet aggregation 50(nM) |
| Compound I | 1.3 |
As can be seen from the above table, the compounds of this invention shows obvious restraining effect in platelet aggregation test.
Claims (3)
1. there is compound and the pharmaceutically acceptable salt thereof of following formula structure,
2. synthesize the method for compound described in claim 1:
Compound II per and compound III are at K
2cO
3catalysis under react, obtain Compound I.
3. compound described in claim 1 or its pharmaceutically purposes of acceptable salt in preparation treatment thrombotic medicine.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410352040.2A CN104086503B (en) | 2014-07-23 | 2014-07-23 | PAR-1 antagonist and uses thereof |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201410352040.2A CN104086503B (en) | 2014-07-23 | 2014-07-23 | PAR-1 antagonist and uses thereof |
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| Publication Number | Publication Date |
|---|---|
| CN104086503A CN104086503A (en) | 2014-10-08 |
| CN104086503B true CN104086503B (en) | 2015-10-14 |
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| CN201410352040.2A Active CN104086503B (en) | 2014-07-23 | 2014-07-23 | PAR-1 antagonist and uses thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN104356060B (en) * | 2014-11-02 | 2016-08-31 | 浙江医药高等专科学校 | The trans cvclohexvl alkyl amide compound of 2-pyridine radicals and purposes |
| CN104356059B (en) * | 2014-11-02 | 2016-08-24 | 浙江医药高等专科学校 | Trans cvclohexvl alkyl amide compound containing halogenated pyridyl and purposes |
| CN104529928A (en) * | 2015-01-13 | 2015-04-22 | 佛山市赛维斯医药科技有限公司 | One category of oxadiazole sulfoxide compounds, and preparation method and application thereof |
| CN104496926B (en) * | 2015-01-13 | 2016-06-01 | 佛山市赛维斯医药科技有限公司 | One class contains compound, the Preparation Method And The Use of diene tetrazole structure |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102241621A (en) * | 2010-05-11 | 2011-11-16 | 江苏恒瑞医药股份有限公司 | 5,5-disubstituted-2-iminopyrrolidine derivatives, preparation method thereof, and medical applications thereof |
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| EA200000048A1 (en) * | 1997-06-19 | 2000-08-28 | Дюпон Фармасьютикалз Компани | INHIBITORS OF FACTOR XA, CONTAINING A GROUP WITH NEUTRAL P1-SPECIFICITY |
| US8673890B2 (en) * | 2009-10-29 | 2014-03-18 | Janssen Pharmaceutica Nv | 2,3-dihydro-1H-isoindol-1-imine derivatives useful as thrombin PAR-1 receptor antagonist |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102241621A (en) * | 2010-05-11 | 2011-11-16 | 江苏恒瑞医药股份有限公司 | 5,5-disubstituted-2-iminopyrrolidine derivatives, preparation method thereof, and medical applications thereof |
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Effective date of registration: 20170725 Address after: 510640 Guangdong City, Tianhe District Province, No. five, road, public education building, unit 371-1, unit 2401 Patentee after: Guangdong Gaohang Intellectual Property Operation Co., Ltd. Address before: 528000 Guangdong, Foshan District, Pu Lan Road, the first floor of the first floor, No. 5, Chancheng Patentee before: Zhang Yuanqiang |
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Effective date of registration: 20170818 Address after: High Zhai River Road Weihai 264200 Shandong province No. 25 Room 401 Patentee after: Zhang Yuanqiang Address before: 510640 Guangdong City, Tianhe District Province, No. five, road, public education building, unit 371-1, unit 2401 Patentee before: Guangdong Gaohang Intellectual Property Operation Co., Ltd. |
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Effective date of registration: 20180515 Address after: 138000 255 Songyuan Road, Songyuan economic and Technological Development Zone, Jilin Patentee after: Jilin century Hank Pharmaceutical Co., Ltd. Address before: 264200 Room 401, No. 25, Zhai he road, Weihai, Shandong Patentee before: Zhang Yuanqiang |