Effect of structural modification on the inhibitory selectivity of rutaecarpine derivatives on human CYP1A1, CYP1A2, and CYP1B1-Reference-Cited by-同舟云学术

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Effect of structural modification on the inhibitory selectivity of rutaecarpine derivatives on human CYP1A1, CYP1A2, and CYP1B1

Published:2003-08 Issue:15 Volume:13 Page:2535-2538
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Don Ming-Jaw,Lewis David F.V.,Wang Shu-Yun,Tsai Mei-Wen,Ueng Yune-Fang

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference21 articles.

1. Human Cytochrome P450 Enzymes: A Status Report Summarizing Their Reactions, Substrates, Inducers, and Inhibitors

2. Guengerich, F. P. In Cytochrome P450, Ortiz de Montellano P. R., Ed., Plenum: New York, 1995; p 473.

3. Murray, G. I., Melvin, W. T., Greenlee, W. F., Burke, M. D. Ann. Rev. Pharmacol. Toxicol. 2001, 41, 297.

4. Molecular modelling of CYP1 family enzymes CYP1A1, CYP1A2, CYP1A6 and CYP1B1 based on sequence homology with CYP102

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