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Angiotensin converting enzyme inhibitors as antihypertensive agents: 1-[(2-mercaptocycloalkyl)carbonyl]-L-prolines.
- Source :
-
Journal of medicinal chemistry [J Med Chem] 1986 Mar; Vol. 29 (3), pp. 411-7. - Publication Year :
- 1986
-
Abstract
- The synthesis of 1-[(2-mercaptocyclopentyl)carbonyl]-L-prolines, 1-[(2-mercaptocyclobutyl)carbonyl]-L-prolines and related benzoyl derivatives as pure isomers is described. The abilities of all the compounds to inhibit angiotensin converting enzyme (ACE) in vitro and in vivo and to lower the systolic blood pressure in renal hypertensive dogs were determined. Three of them, namely 1-[[2-(benzoylthio)cyclopentyl]carbonyl]-L-proline (10f(R,S], 1-[(2-mercaptocyclopentyl)carbonyl]-L-proline (10g(R,S], and 1-[[2-(benzoylthio)cyclobutyl]carbonyl]-L-proline (16f(R,S], were found to be as potent as captopril in reducing blood pressure. The influence of chirality and ring size on the ACE inhibition is described.
- Subjects :
- Animals
Captopril pharmacology
Dogs
Hypertension, Renovascular drug therapy
In Vitro Techniques
Magnetic Resonance Spectroscopy
Male
Proline chemical synthesis
Proline pharmacology
Rats
Rats, Inbred Strains
Stereoisomerism
Structure-Activity Relationship
Sulfides chemical synthesis
Sulfides pharmacology
Angiotensin-Converting Enzyme Inhibitors
Antihypertensive Agents chemical synthesis
Proline analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 0022-2623
- Volume :
- 29
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of medicinal chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 3005576
- Full Text :
- https://doi.org/10.1021/jm00153a017