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Moexiprilat is an inhibitor of angiotensin-converting enzyme (ACE; IC50 = 2.1 nM) and an active metabolite of the prodrug moexipril (Item No. 21255).1 It is formed from moexipril in vivo by side chain ester hydrolysis.2 Moexiprilat (10 nM) prevents the estrone- or angiotensin II-stimulated proliferation of primary neonatal rat cardiac fibroblasts.3 It reduces mean arterial blood pressure and increases the levels of atrial natriuretic peptide, a marker of hypertension, in ovariectomized mice when administered at a dose of 50 mg/kg per day.4
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1. Moexipril, a new angiotensin-
2. Chemical informatics uncovers a new role for moexipril as a novel inhibitor of cAMP phosphodiesterase-
3. Angiotensin converting enzyme inhibition modulates cardiac fibroblast growth. J. Hypertens. 16(3), 377-384 (1998).
4. The influence of oestrogen-