Literature DB >> 6301792

Enalapril maleate (MK-421), a potent, nonsulfhydryl angiotensin-converting enzyme inhibitor: absorption, disposition, and metabolism in man.

E H Ulm.   

Abstract

Animal studies (particularly in dogs) on enalapril maleate have served to predict the patterns of absorption and elimination observed in man. Enalapril is more readily absorbed in man than the active inhibitor form MK-422. Estimates of minimum absorption of enalapril are of the order of 60-70%, based on urinary recovery. Metabolism of enalapril to MK-422 appears to be largely a postabsorptive process. From urinary recovery data, a minimum of 43% of a 10-mg dose of enalapril is available as MK-422. Excretion of enalapril and MK-422 is principally renal. The excellent mass balance obtained in human studies precludes extensive metabolism beyond hydrolysis to MK-422. Data in hand suggest that any metabolism other than to MK-422 is of a trace nature.

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Year:  1983        PMID: 6301792     DOI: 10.3109/03602538308991383

Source DB:  PubMed          Journal:  Drug Metab Rev        ISSN: 0360-2532            Impact factor:   4.518


  15 in total

1.  Role of multidrug resistance-associated protein 4 in the basolateral efflux of hepatically derived enalaprilat.

Authors:  Brian C Ferslew; Kathleen Köck; Arlene S Bridges; Kim L R Brouwer
Journal:  Drug Metab Dispos       Date:  2014-06-23       Impact factor: 3.922

2.  A possible drug interaction between rifampicin and enalapril.

Authors:  D Kandiah; W J Penny; A G Fraser; M J Lewis
Journal:  Eur J Clin Pharmacol       Date:  1988       Impact factor: 2.953

3.  Local inhibition of converting enzyme and vascular responses to angiotensin and bradykinin in the human forearm.

Authors:  N Benjamin; J R Cockcroft; J G Collier; C T Dollery; J M Ritter; D J Webb
Journal:  J Physiol       Date:  1989-05       Impact factor: 5.182

4.  Pharmacokinetics and pharmacodynamics of a novel orally active angiotensin converting enzyme inhibitor (HOE 498) in healthy subjects.

Authors:  P U Witte; R Irmisch; P Hajdú; H Metzger
Journal:  Eur J Clin Pharmacol       Date:  1984       Impact factor: 2.953

5.  The pharmacokinetics of enalapril in hospitalized patients with congestive heart failure.

Authors:  K Dickstein; A E Till; T Aarsland; K Tjelta; A M Abrahamsen; K Kristianson; H J Gomez; H Gregg; M Hichens
Journal:  Br J Clin Pharmacol       Date:  1987-04       Impact factor: 4.335

6.  The effect of enalapril (MK421), an angiotensin converting enzyme inhibitor, on the conscious pregnant ewe and her foetus.

Authors:  F Broughton Pipkin; C P Wallace
Journal:  Br J Pharmacol       Date:  1986-03       Impact factor: 8.739

Review 7.  Enalapril. A review of its pharmacodynamic and pharmacokinetic properties, and therapeutic use in hypertension and congestive heart failure.

Authors:  P A Todd; R C Heel
Journal:  Drugs       Date:  1986-03       Impact factor: 9.546

8.  Pharmacokinetics of ramipril in hypertensive patients with renal insufficiency.

Authors:  H Schunkert; J Kindler; M Gassmann; W Lahn; R Irmisch; E Ritz; E R Debusmann; J O Pujadas; K M Koch; H G Sieberth
Journal:  Eur J Clin Pharmacol       Date:  1989       Impact factor: 2.953

9.  Relative lipophilicities and structural-pharmacological considerations of various angiotensin-converting enzyme (ACE) inhibitors.

Authors:  S A Ranadive; A X Chen; A T Serajuddin
Journal:  Pharm Res       Date:  1992-11       Impact factor: 4.200

Review 10.  An overview of the clinical pharmacology of enalapril.

Authors:  R O Davies; H J Gomez; J D Irvin; J F Walker
Journal:  Br J Clin Pharmacol       Date:  1984       Impact factor: 4.335

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