Synthesis and structure activity relationships of potent new angiotensin converting enzyme inhibitors containing saturated bicyclic amino acids

The synthesis of a series of novel, potent angiotensin converting enzyme (ACE) inhibitors containing saturated bicyclic amino acids in place of proline is described. Octahydroindole-2-carboxylic acid, octahydroisoindole-1-carboxylic acid, and octahydro-3-oxoisoindole-1-carboxylic acid can replace pr...

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Veröffentlicht in:Journal of medicinal chemistry 1987-06, Vol.30 (6), p.992-998
Hauptverfasser: Blankley, C. J, Kaltenbronn, J. S, DeJohn, D. E, Werner, A, Bennett, L. R, Bobowski, G, Krolls, U, Johnson, D. R, Pearlman, W. M
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Sprache:eng
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Zusammenfassung:The synthesis of a series of novel, potent angiotensin converting enzyme (ACE) inhibitors containing saturated bicyclic amino acids in place of proline is described. Octahydroindole-2-carboxylic acid, octahydroisoindole-1-carboxylic acid, and octahydro-3-oxoisoindole-1-carboxylic acid can replace proline in both sulfhydryl and non-sulfhydryl ACE inhibitors to give compounds equipotent to captopril and enalapril both in vitro and in vivo. Structure-activity relationships are discussed. Compound 11a (CI-907, indolapril) has advanced to clinical evaluation.
ISSN:0022-2623
1520-4804
DOI:10.1021/jm00389a006