Identification of metabolic pathways and enzyme systems involved in the in vitro human hepatic metabolism of dronedarone, a potent new oral antiarrhythmic drug

Author:

Klieber Sylvie1,Arabeyre‐Fabre Catherine1,Moliner Patricia1,Marti Eric1,Mandray Martine1,Ngo Robert1,Ollier Céline1,Brun Priscilla1,Fabre Gérard1

Affiliation:

1. SANOFI‐AVENTIS Recherche & Development Disposition Safety and Animal Research Scientific Core Platform Drug Disposition Domain 371 Rue du Professeur Joseph Blayac 34184 Montpellier Cedex 4 France

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,Neurology

Reference21 articles.

1. Cytochrome P450 isoform inhibitors as a tool for the human liver microsomes;Bourrié M;J Pharmacol Exp Ther,1996

2. Pharmacokinetic and pharmacodynamic interactions between metoprolol and dronedarone in extensive and poor CYP2D6 metabolizers healthy subjects

3. Inducibility and expression of class IA and IIIA cytochromes P450 in primary cultures of adult human hepatocytes;Daujat M;Biochem Pharmacol (Life Sci Adv),1990

4. A simple method for screening Monoamine Oxidase (MAO) inhibitory drugs for type preference

5. Characterization of midazolam metabolism using human hepatic musomal fractions and hepatocytes in suspension obtained by perfusing whole human livers

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