Journal of Medicinal Chemistry · 1987 · 44 citations · 0 references
PharmacyMedicinal ChemistryPharmacologyDrug DesignDrug DiscoveryStructure-activity RelationshipsEnzyme InhibitionLigand BindingPotency OptimizationQuantitative Structure-activity RelationshipsStructure-activity Relationship AnalysisAmino AcidsChemical Enzyme InhibitorsChemical Structure-activity RelationshipsMedicinal Chemistry ApplicationsRenin-angiotensin System InhibitorsRenin-angiotensin-aldosterone System InhibitorsResearch Article Structure
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.