Ilaprazole, a new proton pump inhibitor, is primarily metabolized to ilaprazole sulfone by CYP3A4 and 3A5-Reference-Cited by-同舟云学术

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Ilaprazole, a new proton pump inhibitor, is primarily metabolized to ilaprazole sulfone by CYP3A4 and 3A5

Published:2011-10-24 Issue:3 Volume:42 Page:278-284
ISSN:0049-8254
Container-title:Xenobiotica
language:en
Short-container-title:Xenobiotica

Author:

Seo Kyung-Ah,Lee So-Jeong,Kim Kwon-Bok,Bae Soo Kyung,Liu Kwang-Hyeon,Kim Dong-Hyun,Shin Jae-Gook

Publisher

Informa UK Limited

Subject

Health, Toxicology and Mutagenesis,Pharmacology,Toxicology,Biochemistry,General Medicine

Link

http://www.tandfonline.com/doi/pdf/10.3109/00498254.2011.622416

Reference24 articles.

1. Pharmacokinetics and effect on caffeine metabolism of the proton pump inhibitors, omeprazole, lansoprazole, and pantoprazole

2. Ketoconazole and sulphaphenazole as the respective selective inhibitors of P4503A and 2C9

3. Clopidogrel–Drug Interactions

4. Degradation of lansoprazole and omeprazole in the aquatic environment

5. Sex and CYP3A5 genotype influence total CYP3A activity: high CYP3A activity and a unique distribution of CYP3A5 variant alleles in Ethiopians

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