Ethynylflavones, Highly Potent, and Selective Inhibitors of Cytochrome P450 1A1
Author:
Affiliation:
1. Department of Chemistry, Xavier University of Louisiana, New Orleans, Louisiana 70125, United States
2. College of Pharmaceutical Sciences, Capital Medical University, Beijing 100069, PR China
Funder
U.S. Department of Defense
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Toxicology,General Medicine
Link
https://pubs.acs.org/doi/pdf/10.1021/tx5001865
Reference25 articles.
1. The role of cytochrome P450 enzymes in endogenous signalling pathways and environmental carcinogenesis
2. Tissue-specific induction of cytochromes P450 1A1 and 1B1 by polycyclic aromatic hydrocarbons and polychlorinated biphenyls in engineered C57BL/6J mice of arylhydrocarbon receptor gene
3. Plasmid-mediated expression of the UmuDC mutagenesis proteins in an Escherichia coli strain engineered for human cytochrome P450 1A2-catalyzed activation of aromatic amines
4. Cytochrome P450 CYP1A1: wider roles in cancer progression and prevention
5. Organ-Specific Roles of CYP1A1 during Detoxication of Dietary Benzo[a]pyrene
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