Inhibition of cytochrome P450 by ethambutol in human liver microsomes-Reference-Cited by-同舟云学术

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Inhibition of cytochrome P450 by ethambutol in human liver microsomes

Published:2014-08 Issue:1 Volume:229 Page:33-40
ISSN:0378-4274
Container-title:Toxicology Letters
language:en
Short-container-title:Toxicology Letters

Author:

Lee Sang Yoon,Jang Himchan,Lee Ji-Yoon,Kwon Kwang-il,Oh Soo Jin,Kim Sang Kyum

Funder

Korea Food and Drug Administration

Korea Healthcare Technology R&D Project

Ministry for Health, Welfare & Family Affairs, Republic of Korea

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference26 articles.

1. Effect of combined therapy of oral anti-tubercular agents on theophylline pharmacokinetics;Ahn;Int. J. Tuberc. Lung Dis.,2000

2. The area under the plasma concentration–time curve for oral midazolam is 400-fold larger during treatment with itraconazole than with rifampicin;Backman;Eur. J. Clin. Pharmacol.,1998

3. An examination of IC50 and IC50-shift experiments in assessing time-dependent inhibition of CYP3A4, CYP2D6 and CYP2C9 in human liver microsomes;Berry;Drug Metab. Lett.,2008

4. Effect of rifabutin on ethambutol pharmacokinetics in healthy volunteers;Breda;Pharmacol. Res.,1999

5. Low daily 10-mg and 20-mg doses of fluvoxamine inhibit the metabolism of both caffeine (cytochrome P4501A2) and omeprazole (cytochrome P4502C19);Christensen;Clin. Pharmacol. Ther.,2002

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