Abstract
A series of biphenyl imidazolinones were synthesized as nonpeptide angiotensin II receptor antagonists. While those compounds with a tetrazole functionality were found to be AT 1 selective, those with a sulfonamide moiety showed affinities for both the AT 1 and the AT 2 sites. Representative compounds were very active in lowering blood pressure in conscious renal hypertensive rats following intravenous administration.
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