ES471791A1 - Un procedimiento para la preparacion de un peptido - Google Patents
Un procedimiento para la preparacion de un peptidoInfo
- Publication number
- ES471791A1 ES471791A1 ES471791A ES471791A ES471791A1 ES 471791 A1 ES471791 A1 ES 471791A1 ES 471791 A ES471791 A ES 471791A ES 471791 A ES471791 A ES 471791A ES 471791 A1 ES471791 A1 ES 471791A1
- Authority
- ES
- Spain
- Prior art keywords
- preparation
- peptide
- procedure
- disclosed
- hydroxyacetyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 108090000765 processed proteins & peptides Proteins 0.000 title 1
- 102000005862 Angiotensin II Human genes 0.000 abstract 1
- 101800000733 Angiotensin-2 Proteins 0.000 abstract 1
- 239000002253 acid Chemical group 0.000 abstract 1
- 125000001980 alanyl group Chemical group 0.000 abstract 1
- -1 alpha -hydroxypropyl Chemical group 0.000 abstract 1
- 125000000350 glycoloyl group Chemical group O=C([*])C([H])([H])O[H] 0.000 abstract 1
- 125000000741 isoleucyl group Chemical group [H]N([H])C(C(C([H])([H])[H])C([H])([H])C([H])([H])[H])C(=O)O* 0.000 abstract 1
- 125000001909 leucine group Chemical group [H]N(*)C(C(*)=O)C([H])([H])C(C([H])([H])[H])C([H])([H])[H] 0.000 abstract 1
- 206010038464 renal hypertension Diseases 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000000341 threoninyl group Chemical group [H]OC([H])(C([H])([H])[H])C([H])(N([H])[H])C(*)=O 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K7/00—Peptides having 5 to 20 amino acids in a fully defined sequence; Derivatives thereof
- C07K7/04—Linear peptides containing only normal peptide links
- C07K7/14—Angiotensins: Related peptides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Molecular Biology (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Vascular Medicine (AREA)
- Biochemistry (AREA)
- Biophysics (AREA)
- Genetics & Genomics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Un procedimiento para la preparación de un péptido de la fórmula general I X-Arg-Val-Tir-Ile-His-Pro-Y (I) donde X es un radical derivado de un ácido alfa-hidroxicarboxílico alifático, e Y es un radical derivado de un ácido alfa-aminocarboxílico alifático y sales de adición de ácido y complejos de aquél, que comprende hacer reaccionar un derivado de heptapéptico reactivo de la fórmula general II H-Arg(A)-Val-Tir(B)-Ile-His(E)-Pro-Y-OG (II) donde A representa un grupo adecuado para una protección temporal del grupo guanidino de Arg, B representa un grupo adecuado para una protección temporal del grupo hidroxilo aromático de Tir, E es un grupo adecuado para una protección temporal del grupo imidazol de His, y G representa un grupo adecuado para la protección del grupo carboxilo del aminoácido alifático terminal C, el cual grupo protector es estable en condiciones ácidas suaves pero puede escindirse por medio de ácidos o bases fuertes o por hidrogenación catalítica.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU77RI641A HU177134B (en) | 1977-07-18 | 1977-07-18 | Process for preparing angiotensin ii analogues containing alpha-hydroxy-acid in position 1 with angiotensin ii antagonist activity |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES471791A1 true ES471791A1 (es) | 1979-02-01 |
Family
ID=11001038
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES471791A Expired ES471791A1 (es) | 1977-07-18 | 1978-07-17 | Un procedimiento para la preparacion de un peptido |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US4209442A (es) |
| JP (1) | JPS5831337B2 (es) |
| AT (1) | AT360678B (es) |
| AU (1) | AU520176B2 (es) |
| BE (1) | BE869076A (es) |
| CA (1) | CA1114810A (es) |
| CH (1) | CH637916A5 (es) |
| CS (1) | CS201013B2 (es) |
| DD (1) | DD137221A5 (es) |
| DE (1) | DE2831271C2 (es) |
| DK (1) | DK319578A (es) |
| ES (1) | ES471791A1 (es) |
| FI (1) | FI64797C (es) |
| FR (1) | FR2398049A1 (es) |
| GB (1) | GB2002779B (es) |
| HU (1) | HU177134B (es) |
| IL (1) | IL55075A (es) |
| IN (1) | IN149852B (es) |
| NL (1) | NL7807627A (es) |
| NO (1) | NO148070C (es) |
| PL (1) | PL111964B1 (es) |
| SE (1) | SE444439B (es) |
| SU (1) | SU913940A3 (es) |
| YU (1) | YU41315B (es) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2905502C2 (de) * | 1979-02-14 | 1982-07-15 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung von LH-RH bzw. LH-RH-Analoga und Pyroglutamyl-N↑i↑m↑-dinitrophenyl-histidin |
| HU181008B (en) * | 1980-01-18 | 1983-05-30 | Richter Gedeon Vegyeszet | Process for producing angiotenzin-ii analogues of antagonistic activity containing sarcosyl-group at the 1-positon,and an alpha-hydroxy-carboxylic acid at the 8-position |
| HU181009B (en) * | 1980-01-18 | 1983-05-30 | Richter Gedeon Vegyeszet | Process for preparing angiotensin-ii analogues with antagonictic activity containing in position 1 sarcosyl,hydroxyacetyl or l-alpha-aminoxy-propionyl group and in positiona 8 esteric group |
| FR2546163B1 (fr) * | 1983-05-16 | 1987-10-09 | Centre Nat Rech Scient | Nouveaux derives acyles hydrosolubles de peptides ou d'amino-acides, leur preparation et leur application |
| HU191961B (en) * | 1984-08-02 | 1987-04-28 | Richter Gedeon Vegyeszet | Process for producing 1,5 and 8 substituted peptides of angiotenzin-ii antagonistic activity |
| US5182264A (en) * | 1986-03-07 | 1993-01-26 | Schering Corporation | Angiotensin II receptor blockers as antiglaucoma agents |
| US4772684A (en) * | 1987-01-20 | 1988-09-20 | Triton Biosciences, Inc. | Peptides affecting blood pressure regulation |
| US7012066B2 (en) * | 2000-07-21 | 2006-03-14 | Schering Corporation | Peptides as NS3-serine protease inhibitors of hepatitis C virus |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3886134A (en) * | 1970-03-09 | 1975-05-27 | Morton Norwich Products Inc | Analogues of angiotensin II |
| GB1320104A (en) * | 1971-05-20 | 1973-06-13 | Norwich Pharma Co | Hepta-and octapeptides |
| US3907762A (en) * | 1971-12-27 | 1975-09-23 | Univ Sherbrooke | Angiotensin{hd II {B position 8 analogs |
| DE2323322A1 (de) * | 1973-05-09 | 1974-11-28 | Hoechst Ag | Neue peptide mit blutdrucksenkender wirkung und verfahren zu ihrer herstellung |
| US3923771A (en) * | 1974-05-10 | 1975-12-02 | Francis Merlin Bumpus | N-Guanidylacetyl-{8 des-asp{hu 1{b -Ile{hu 8{b {9 {0 angiotensin II as an angiotensin antagonist |
-
1977
- 1977-07-18 HU HU77RI641A patent/HU177134B/hu not_active IP Right Cessation
-
1978
- 1978-07-04 IL IL55075A patent/IL55075A/xx unknown
- 1978-07-10 IN IN760/CAL/78A patent/IN149852B/en unknown
- 1978-07-11 FI FI782216A patent/FI64797C/fi not_active IP Right Cessation
- 1978-07-11 US US05/923,663 patent/US4209442A/en not_active Expired - Lifetime
- 1978-07-13 FR FR7821045A patent/FR2398049A1/fr active Granted
- 1978-07-13 SE SE7807824A patent/SE444439B/sv not_active IP Right Cessation
- 1978-07-13 AU AU38009/78A patent/AU520176B2/en not_active Expired
- 1978-07-17 NO NO782464A patent/NO148070C/no unknown
- 1978-07-17 YU YU1715/78A patent/YU41315B/xx unknown
- 1978-07-17 ES ES471791A patent/ES471791A1/es not_active Expired
- 1978-07-17 DD DD78206762A patent/DD137221A5/xx unknown
- 1978-07-17 DK DK319578A patent/DK319578A/da not_active Application Discontinuation
- 1978-07-17 SU SU782639848A patent/SU913940A3/ru active
- 1978-07-17 CA CA307,496A patent/CA1114810A/en not_active Expired
- 1978-07-17 NL NL7807627A patent/NL7807627A/xx not_active Application Discontinuation
- 1978-07-17 GB GB7830046A patent/GB2002779B/en not_active Expired
- 1978-07-17 CH CH771878A patent/CH637916A5/de not_active IP Right Cessation
- 1978-07-17 CS CS784757A patent/CS201013B2/cs unknown
- 1978-07-17 DE DE2831271A patent/DE2831271C2/de not_active Expired
- 1978-07-18 BE BE189342A patent/BE869076A/xx not_active IP Right Cessation
- 1978-07-18 JP JP53087646A patent/JPS5831337B2/ja not_active Expired
- 1978-07-18 AT AT518378A patent/AT360678B/de active
- 1978-07-18 PL PL1978208497A patent/PL111964B1/pl unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD1A | Patent lapsed |
Effective date: 19971103 |