Development of anin vivorat screen model to predict pharmacokinetic interactions of CYP3A4 substrates-Reference-Cited by-同舟云学术

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Development of anin vivorat screen model to predict pharmacokinetic interactions of CYP3A4 substrates

Published:2007-09 Issue:9 Volume:37 Page:923-942
ISSN:0049-8254
Container-title:Xenobiotica
language:en
Short-container-title:Xenobiotica

Author:

Mandlekar S. V.,Rose A. V.,Cornelius G.,Sleczka B.,Caporuscio C.,Wang J.,Marathe P. H.

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1080/00498250701570269

Reference66 articles.

1. Rofecoxib is a potent inhibitor of cytochrome P450 1A2: studies with tizanidine and caffeine in healthy subjects

2. Erythromycin-felodipine interaction: Magnitude, mechanism, and comparison with grapefruit juice*

3. Current methodologies used for evaluation of intestinal permeability and absorption

4. Utility of 96 well Caco-2 cell system for increased throughput of P-gp screening in drug discovery

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4. Humanized UGT2 and CYP3A transchromosomic rats for improved prediction of human drug metabolism;Proceedings of the National Academy of Sciences;2019-02-04

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