In Vitro Metabolism of Montelukast by Cytochrome P450s and UDP-Glucuronosyltransferases

Author:

Cardoso Josiane de Oliveira,Oliveira Regina Vincenzi,Lu Jessica Bo Li,Desta Zeruesenay

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference32 articles.

1. CYP2C8 Activity Recovers within 96 Hours after Gemfibrozil Dosing: Estimation of CYP2C8 Half-Life Using Repaglinide as an in Vivo Probe

2. Metabolic profiles of montelukast sodium (Singulair), a potent cysteinyl leukotriene1 receptor antagonist, in human plasma and bile;Balani;Drug Metab Dispos,1997

3. Quantification of montelukast, a selective cysteinyl leukotriene receptor (CysLT1) antagonist in human plasma by liquid chromatography-mass spectrometry: validation and its application to a human pharmacokinetic study

4. Hepatic microsomal metabolism of montelukast, a potent leukotriene D4 receptor antagonist, in humans;Chiba;Drug Metab Dispos,1997

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