FI870474A0 - Med svavelhaltiga grupper substituerade 5-amino-4-hydroxivalerylderivat. - Google Patents
Med svavelhaltiga grupper substituerade 5-amino-4-hydroxivalerylderivat.Info
- Publication number
- FI870474A0 FI870474A0 FI870474A FI870474A FI870474A0 FI 870474 A0 FI870474 A0 FI 870474A0 FI 870474 A FI870474 A FI 870474A FI 870474 A FI870474 A FI 870474A FI 870474 A0 FI870474 A0 FI 870474A0
- Authority
- FI
- Finland
- Prior art keywords
- svavelhaltiga
- hydroxivalerylderivat
- grupper
- substituerade
- med
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/84—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S530/00—Chemistry: natural resins or derivatives; peptides or proteins; lignins or reaction products thereof
- Y10S530/86—Renin inhibitors
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Medicinal Chemistry (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH48686 | 1986-02-07 | ||
CH334786 | 1986-08-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
FI870474A0 true FI870474A0 (fi) | 1987-02-04 |
FI870474A FI870474A (fi) | 1987-08-08 |
Family
ID=25684707
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI870474A FI870474A (fi) | 1986-02-07 | 1987-02-04 | Med svavelhaltiga grupper substituerade 5-amino-4-hydroxivalerylderivat. |
Country Status (11)
Country | Link |
---|---|
US (2) | US4889869A (fi) |
EP (1) | EP0236734A3 (fi) |
KR (1) | KR910002388B1 (fi) |
AU (1) | AU608746B2 (fi) |
DK (1) | DK61887A (fi) |
FI (1) | FI870474A (fi) |
HU (1) | HU204286B (fi) |
IL (1) | IL81482A (fi) |
NO (1) | NO870477L (fi) |
NZ (1) | NZ219186A (fi) |
PT (1) | PT84249B (fi) |
Families Citing this family (29)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0364493A1 (en) * | 1987-08-07 | 1990-04-25 | The Upjohn Company | Renin inhibiting peptides with nonpeptide linkages |
EP0309766B1 (en) * | 1987-09-29 | 1998-04-15 | Banyu Pharmaceutical Co., Ltd. | N-acylamino acid derivatives and their use |
JPH0262856A (ja) * | 1987-09-29 | 1990-03-02 | Banyu Pharmaceut Co Ltd | 新規n−アシルアミノ酸誘導体及びその用途 |
DE3804793A1 (de) * | 1988-02-16 | 1989-08-24 | Hoechst Ag | Renin-hemmende aminosaeurederivate |
DE3805156A1 (de) * | 1988-02-19 | 1989-08-31 | Merck Patent Gmbh | Aminosaeurederivate |
EP0347987A3 (en) * | 1988-06-20 | 1991-01-02 | Merck & Co. Inc. | Tripeptide renin inhibitors with n-terminal carbamoyl or acyl groups |
US5428061A (en) * | 1988-09-15 | 1995-06-27 | Schwarz Pharma Ag | Organic nitrates and method for their preparation |
EP0475255A3 (en) * | 1990-09-12 | 1993-04-14 | F. Hoffmann-La Roche Ag | Process for the preparation of optically pure (s)-alpha-((tert-butylsulfonyl)methyl)hydro cinnamic acid |
DE59207226D1 (de) | 1991-07-03 | 1996-10-31 | Ciba Geigy Ag | Pharmakologisch wirksame Hydrazinderivate und Verfahren zu deren Herstellung |
US5246969A (en) * | 1992-07-20 | 1993-09-21 | G. D. Searle & Co. | Di-propargyl-containing aryl/alkylsulfonyl-terminated alanine amino-diol compounds for treatment of hypertension |
US5317039A (en) * | 1992-07-20 | 1994-05-31 | G. D. Searle & Co. | Cyclopropyl-alanine aryl/alkylsulfide/sulfonyl-terminated amino-diol compounds for treatment of hypertension |
US5314920A (en) * | 1992-07-20 | 1994-05-24 | G. D. Searle & Co. | Ethynyl-alanine aryl/alkylsulfonyl-terminated amino-diol compounds for treatment of hypertension |
US5268391A (en) * | 1992-07-20 | 1993-12-07 | C. D. Searle & Co. | Propargyl-terminated cycloalkylalkyl-P2-site substituted aryl/alkylsulfonyl-terminated alanine amino-diol compounds for treatment of hypertension |
US5312838A (en) * | 1992-09-21 | 1994-05-17 | G. D. Searle & Co. | β-alanineamide aryl/alkylsulfide/sulfonyl-terminated amino-diol compounds for treatment of hypertension |
DE59303870D1 (de) | 1992-12-23 | 1996-10-24 | Ciba Geigy Ag | Antiretrovirale hydrazinderivate |
IL108924A0 (en) * | 1993-03-19 | 1994-06-24 | Ciba Vision Ag | Compositions for the treatment of eye diseases |
US5414018A (en) * | 1993-09-24 | 1995-05-09 | G. D. Searle & Co. | Alkylaminoalkyl-terminated sulfide/sulfonyl-containing propargyl amino-diol compounds for treatment of hypertension |
US5416119A (en) * | 1993-10-25 | 1995-05-16 | G. D. Searle & Co. | Alkylaminoalkyl-terminated sulfide/sulfonyl-containing cycloalkyl-alanine amino-diol compounds for treatment of hypertension |
US5432201A (en) * | 1993-11-22 | 1995-07-11 | G. D. Searle & Co. | Alkylaminoalkyl-sulfonyl-terminated β-alanineamide amino-diol compounds for treatment of hypertension |
US6206010B1 (en) * | 2000-04-07 | 2001-03-27 | Abdo Malki | Credit card shaped grooming device |
CN1319987C (zh) | 2002-04-24 | 2007-06-06 | 森启 | γ-分泌酶抑制剂 |
EP1897879A3 (en) | 2005-03-31 | 2008-06-11 | Speedel Experimenta AG | 2,4,5-substituted piperidines as renin inhibitors |
EP1745778A3 (en) | 2005-07-20 | 2007-03-07 | Speedel Experimenta AG | Diaminoalcohols as therapeutic compounds |
US20070021400A1 (en) | 2005-07-20 | 2007-01-25 | Peter Herold | Amino alcohols as therapeutic compounds |
US20070021399A1 (en) | 2005-07-20 | 2007-01-25 | Peter Herold | Amido-amino alcohols as therapeutic compounds |
EP1958634A3 (en) | 2007-02-14 | 2008-09-24 | Speedel Experimenta AG | Substituted piperidines as inhibitors of beta-secretase, cathepsin D, plasmepsin II and/or HIV protease |
CA2769186C (en) | 2009-08-11 | 2016-10-04 | Novartis Ag | The ring opening of lactones and lactams |
GB201401520D0 (en) * | 2014-01-29 | 2014-03-12 | Batmark Ltd | Aerosol-forming member |
CN106542961B (zh) * | 2016-11-04 | 2019-02-01 | 山东铂源药业有限公司 | 一种消旋卡多曲中间体的合成方法 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4198398A (en) * | 1977-07-12 | 1980-04-15 | Derek Hudson | Enkephalin analogues |
US4372974A (en) * | 1980-06-25 | 1983-02-08 | New York University | Anticonvulsive compositions and method of treating convulsive disorders |
NO812612L (no) * | 1980-08-06 | 1982-02-08 | Ferring Pharma Ltd | Enzym-inhibitorer. |
US4609643A (en) * | 1980-08-06 | 1986-09-02 | Aktiebolaget Hassle | Renin inhibitors, treatments and dipeptide synthesis |
US4478826A (en) * | 1981-10-08 | 1984-10-23 | Merck & Co., Inc. | Renin inhibitory peptides |
US4435329A (en) * | 1981-10-16 | 1984-03-06 | American Cyanamid Company | Substituted N-(ω-aroylpropionyl) derivatives of α-amino acids and esters thereof |
US4470971A (en) * | 1981-10-19 | 1984-09-11 | Merck & Co., Inc. | Renin inhibitory peptides having His13 |
US4479941A (en) * | 1981-12-10 | 1984-10-30 | Merck & Co., Inc. | Renin inhibitory peptides having PHE13 delection |
AU573735B2 (en) * | 1983-02-07 | 1988-06-23 | Aktiebolaget Hassle | Peptide analogue enzyme inhibitors |
US4722810A (en) * | 1984-08-16 | 1988-02-02 | E. R. Squibb & Sons, Inc. | Enkephalinase inhibitors |
EP0136883B1 (en) * | 1983-10-03 | 1987-11-25 | E.R. Squibb & Sons, Inc. | Enkephalinase inhibitors |
US4613676A (en) * | 1983-11-23 | 1986-09-23 | Ciba-Geigy Corporation | Substituted 5-amino-4-hydroxyvaleryl derivatives |
JPS60163899A (ja) * | 1984-02-03 | 1985-08-26 | Sankyo Co Ltd | レニン阻害ペプチド類 |
US4661473A (en) * | 1984-03-27 | 1987-04-28 | Merck & Co., Inc. | Renin inhibitors containing peptide isosteres |
US4645759A (en) * | 1984-06-22 | 1987-02-24 | Abbott Laboratories | Renin inhibiting compounds |
DK356085A (da) * | 1984-08-06 | 1986-02-07 | Upjohn Co | Reninhaemmende peptid eller et farmaceutisk acceptabelt syreadditionssalt deraf |
US4727060A (en) * | 1984-11-13 | 1988-02-23 | Ciba-Geigy Corporation | Novel 5-amino-4-hydroxyvaleryl derivatives |
US4665193A (en) * | 1984-12-14 | 1987-05-12 | E. R. Squibb & Sons, Inc. | Amino acid ester renin inhibitors |
US4729985A (en) * | 1985-08-09 | 1988-03-08 | Pfizer Inc. | Renin inhibitors containing 5-amino-2,5-disubstituted-4-hydroxypentanoic acid residues |
US4758584A (en) * | 1987-02-05 | 1988-07-19 | Ciba-Geigy Corporation | Antihypertensive 5-amino-4-hydroxyvaleryl derivatives substituted by sulphur-containing groups |
FI89058C (fi) * | 1987-02-27 | 1993-08-10 | Yamanouchi Pharma Co Ltd | Foerfarande foer framstaellning av som remin-inhibitorer anvaenda 2-(l-alanyl-l-histidylamino)-butanol-derivat |
US4921855A (en) * | 1987-06-22 | 1990-05-01 | Fujisawa Pharmaceutical Co., Ltd. | New Histidyl amino acid derivatives, and pharmaceutical composition comprising the same |
-
1987
- 1987-02-04 FI FI870474A patent/FI870474A/fi not_active IP Right Cessation
- 1987-02-04 EP EP87101502A patent/EP0236734A3/de not_active Withdrawn
- 1987-02-05 PT PT84249A patent/PT84249B/pt not_active IP Right Cessation
- 1987-02-05 NZ NZ219186A patent/NZ219186A/en unknown
- 1987-02-05 IL IL81482A patent/IL81482A/xx unknown
- 1987-02-06 DK DK061887A patent/DK61887A/da not_active Application Discontinuation
- 1987-02-06 AU AU68595/87A patent/AU608746B2/en not_active Ceased
- 1987-02-06 KR KR1019870000948A patent/KR910002388B1/ko not_active IP Right Cessation
- 1987-02-06 HU HU87471A patent/HU204286B/hu not_active IP Right Cessation
- 1987-02-06 NO NO870477A patent/NO870477L/no unknown
-
1989
- 1989-04-19 US US07/341,239 patent/US4889869A/en not_active Expired - Fee Related
- 1989-09-08 US US07/405,372 patent/US4914129A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US4889869A (en) | 1989-12-26 |
IL81482A (en) | 1991-04-15 |
NO870477D0 (no) | 1987-02-06 |
KR910002388B1 (ko) | 1991-04-20 |
DK61887D0 (da) | 1987-02-06 |
NZ219186A (en) | 1990-01-29 |
AU608746B2 (en) | 1991-04-18 |
EP0236734A2 (de) | 1987-09-16 |
AU6859587A (en) | 1987-08-13 |
HUT43619A (en) | 1987-11-30 |
HU204286B (en) | 1991-12-30 |
NO870477L (no) | 1987-08-10 |
IL81482A0 (en) | 1987-09-16 |
PT84249B (pt) | 1989-09-14 |
EP0236734A3 (de) | 1988-05-11 |
FI870474A (fi) | 1987-08-08 |
US4914129A (en) | 1990-04-03 |
KR870007947A (ko) | 1987-09-23 |
DK61887A (da) | 1987-08-08 |
PT84249A (en) | 1987-03-01 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM | Patent lapsed |
Owner name: CIBA-GEIGY AG |