are disclosed. These compounds inhibit the angiotensinogen-cleaving action of the natural proteolytic enzyme, renin, and are useful in treating, preventing or managing renin-associated hypertension, hyperaldosteronism, congestive heart failure, and glaucoma.
are disclosed. These compounds inhibit the angiotensinogen-cleaving action of the natural proteolytic enzyme, renin, and are useful in treating, preventing or managing renin-associated hypertension, hyperaldosteronism, congestive heart failure, and glaucoma.
摘要:
There are disclosed substituted imidazole derivatives of Formula I bearing acidic functional groups which are useful as angiotensin II antagonists.
摘要:
Angiotensin converting enzyme inhibitors with a lactam ring of 7-9 members and bicyclic analogs either alone or in combination with carbonic anhydrase inhibitors are useful in the treatment of glaucoma and ocular hypertension associated therewith.
摘要:
Substituted Imidazo-fused 6-membered heterocycles of structural formula: wherein A, B, C, and D are independently carbon atoms or nitrogen atoms are angiotensin II antagonists useful in the treatment of hypertension and congestive heart failure.
摘要:
Dipeptides which contain phosphorus and their pharmaceutical use and preparation are disclosed. The compounds have dehydropeptidase (DHP) enzyme inhibitor activity.
摘要:
Peptides of the formula A-B-D-E-G are disclosed wherein A is, e.g., benzyloxycarbonyl, t-butoxycarbonyl, 1-naphthyloxyacetyl or 1-naphthylacetyl; B is, e.g., phenylalanine, 3-(1-naphthyl)alanine, tryptophan or homophenylalanine; D is, e.g., histidine, lysine or phenylalanine; E is, e.g., one of the following formulae: or and G is, e.g., -OH, -OEt, -NH 2 . Those compounds inhibit enzymes and can be used as pharmaceutical agents.