| Literature DB >> 1542102 |
D M Floyd1, S D Kimball, J Krapcho, J Das, C F Turk, R V Moquin, M W Lago, K J Duff, V G Lee, R E White.
Abstract
As part of a program to discover potent antihypertensive analogues of diltiazem (3a), we prepared 1-benzazepin-2-ones (4). Benzazepinones competitively displace radiolabeled diltiazem, and show the same absolute stereochemical preferences at the calcium channel receptor protein. Derivatives of 4 containing a trifluoromethyl substituent in the fused aromatic ring show potent and long-acting antihypertensive activity. Studies of the metabolism of 4 lead to the metabolically stable antihypertensive calcium channel blockers 5a and 5c. Benzazepinone 5a is a longer acting and more potent antihypertensive agent than the second generation diltiazem analogue TA-3090 (3e).Entities:
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Year: 1992 PMID: 1542102 DOI: 10.1021/jm00082a018
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446