Variation in Expression of Cytochrome P450 3A Isoforms and Toxicological Effects: Endo- and Exogenous Substances as Regulatory Factors and Substrates
Author:
Affiliation:
1. Laboratory of Clinical Pharmaceutics and Therapeutics, College of Pharmaceutical Sciences, Ritsumeikan University
2. School of Pharmaceutical Sciences, Wakayama Medical University
Publisher
Pharmaceutical Society of Japan
Subject
Pharmaceutical Science,Pharmacology,General Medicine
Link
https://www.jstage.jst.go.jp/article/bpb/44/11/44_b21-00332/_pdf
Reference219 articles.
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2. 2) Huang W, Lin YS, McConn DJ 2nd, Calamia JC, Totah RA, Isoherranen N, Glodowski M, Thummel KE. Evidence of significant contribution from CYP3A5 to hepatic drug metabolism. Drug Metab. Dispos., 32, 1434–1445 (2004). doi: 10.1124/dmd.104.001313.
3. 3) Li X, Song X, Kamenecka TM, Cameron MD. Discovery of a highly selective CYP3A4 inhibitor suitable for reaction phenotyping studies and differentiation of CYP3A4 and CYP3A5. Drug Metab. Dispos., 40, 1803–1809 (2012). doi: 10.1124/dmd.112.046144.
4. 4) Wu JJ, Cao YF, Feng L, He YQ, Hong JY, Dou TY, Wang P, Hao DC, Ge GB, Yang L. A naturally occurring isoform-specific probe for highly selective and sensitive detection of human cytochrome P450 3A5. J. Med. Chem., 60, 3804–3813 (2017). doi: 10.1021/acs.jmedchem.7b00001.
5. 5) Xue Y, Li J, Wu Z, Liu G, Tang Y, Li W. Computational insights into the different catalytic activities of CYP3A4 and CYP3A5 toward schisantherin E. Chem. Biol. Drug Des., 93, 854–864 (2019). doi: 10.1111/cbdd.13475.
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