Inactivation kinetics and residual activity of CYP3A4 after treatment with erythromycin-Reference-Cited by-同舟云学术

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Inactivation kinetics and residual activity of CYP3A4 after treatment with erythromycin

Published:2017-07-13 Issue:7 Volume:38 Page:420-425
ISSN:0142-2782
Container-title:Biopharmaceutics & Drug Disposition
language:en
Short-container-title:Biopharm Drug Dispos

Author:

Ishikawa Yuko¹,Akiyoshi Takeshi¹,Imaoka Ayuko¹,Ohtani Hisakazu¹

Affiliation:

1. Keio University Faculty of Pharmacy 1-5-30; Shibakoen Minato-ku Tokyo 105-8512 Japan

Funder

JSPS Kakenhi

Publisher

Wiley

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine

Reference24 articles.

1. Mechanism-based inhibition profiles of erythromycin and clarithromycin with cytochrome P450 3A4 genetic variants;Akiyoshi;Drug Metabolism and Pharmacokinetics,2013

2. Multisite kinetic analysis of interactions between prototypical CYP3A4 subgroup substrates: Midazolam, testosterone, and nifedipine;Aleksandra;Drug Metabolism and Disposition,2003

3. Structural basis for ligand promiscuity in cytochrome P450 3A4;Ekroos;Proceedings of the National Academy of Science USA,2006

4. In vitro and in vivo glucuronidation of midazolam in humans;Hyland;British Journal of Clinical Pharmacology,2009

5. Prediction of the in vivo interaction between midazolam and macrolides based on in vitro studies using human liver microsomes;Ito;Drug Metabolism and Disposition,2003

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2. Time-dependent inhibition of CYP3A4-mediated midazolam metabolism by macrolide antibiotics in CYP3A4 genetic variants: Comparison with testosterone metabolism;Int. Journal of Clinical Pharmacology and Therapeutics;2021-12-01

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4. Inhibitory kinetics of fruit components on CYP2C19 activity;Drug Metabolism and Pharmacokinetics;2019-06

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