| Literature DB >> 3039132 |
A A Hagedorn, P W Erhardt, W C Lumma, R A Wohl, E Cantor, Y L Chou, W R Ingebretsen, J W Lampe, D Pang, C A Pease.
Abstract
A series of 4-alkyl-1,3-dihydro-5-[(1H-imidazolyl)benzoyl]-2H-imidazol-2-ones 9 was synthesized and evaluated in vitro for positive inotropic and cyclic AMP phosphodiesterase inhibitory activity. A wide range of inotropic and enzyme-inhibitory potencies was observed, substitution on the imidazolyl moiety being the major determinant of activity. The 4-ethyl-5-[4-(1H-imidazol-1-yl)benzoyl] congener 9g exhibited the highest potency in vitro. Incorporation of a methyl group at the imidazolyl 2-position gave 9h, which was less potent but remarkably selective in vivo for positive inotropic effects over heart rate and hypotensive effects.Entities:
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Year: 1987 PMID: 3039132 DOI: 10.1021/jm00391a013
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446