Physiologically Based Pharmacokinetic Model of Mechanism-Based Inhibition of CYP3A by Clarithromycin-Reference-Cited by-同舟云学术

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Physiologically Based Pharmacokinetic Model of Mechanism-Based Inhibition of CYP3A by Clarithromycin

Published:2009-11-02 Issue:2 Volume:38 Page:241-248
ISSN:0090-9556
Container-title:Drug Metabolism and Disposition
language:en
Short-container-title:Drug Metab Dispos

Author:

Quinney Sara K.,Zhang Xin,Lucksiri Aroonrut,Gorski J. Christopher,Li Lang,Hall Stephen D.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmaceutical Science,Pharmacology

Reference45 articles.

1. Physiological Parameter Values for Physiologically Based Pharmacokinetic Models

2. STOCHASTIC PREDICTION OF CYP3A-MEDIATED INHIBITION OF MIDAZOLAM CLEARANCE BY KETOCONAZOLE

3. Single- and Multiple-dose Pharmacokinetics of Clarithromycin, a New Macrolide Antimicrobial

4. Pharmacokinetics of clarithromycin, a new macrolide, after single ascending oral doses

5. Comparison of different approaches to predict metabolic drug-drug interactions

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