Effects of xenobiotics on CYP1 enzyme-mediated biotransformation and bioactivation of estradiol-Reference-Cited by-同舟云学术

Effects of xenobiotics on CYP1 enzyme-mediated biotransformation and bioactivation of estradiol

Published:2023-02-23 Issue:1-2 Volume:55 Page:1-49
ISSN:0360-2532
Container-title:Drug Metabolism Reviews
language:en
Short-container-title:Drug Metabolism Reviews

Author:

Mao Xu¹^ORCID,Li Hui²,Zheng Jiang³⁴

Affiliation:

1. Department of Pharmaceutical Analysis, College of Pharmacy, Mudanjiang Medical University, Mudanjiang, China

2. Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, AZ, USA

3. State Key Laboratory of Functions and Applications of Medicinal Plants, Key Laboratory of Pharmaceutics of Guizhou Province, Guizhou Medical University, Guiyang, China

4. Key Laboratory of Environmental Pollution Monitoring and Disease Control, Ministry of Education, Guizhou Medical University, Guiyang, China

Funder

Natural Science Foundation of Heilongjiang Province of China

Fundamental Scientific Research Fund for Higher Education Institutions of Heilongjiang Province of China

PhD Research Startup Foundation of Mudanjiang Medical University of Heilongjiang Province of China

Publisher

Informa UK Limited

Subject

Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics

Link

https://www.tandfonline.com/doi/pdf/10.1080/03602532.2023.2177671

Reference183 articles.

1. In Vitro inhibitory potential of decursin and decursinol angelate on the catalytic activity of cytochrome P-450 1A1/2, 2D15, and 3A12 isoforms in canine hepatic microsomes

2. Non-irradiation-derived reactive oxygen species (ROS) and cancer: therapeutic implications

3. Ellipticine and benzo(a)pyrene increase their own metabolic activation via modulation of expression and enzymatic activity of cytochromes P450 1A1 and 1A2

4. ANTITUMOR DRUG ELLIPTICINE INHIBITS THE ACTIVITIES OF RAT HEPATIC CYTOCHROMES P450

5. The Anticancer Drug Ellipticine Is a Potent Inducer of Rat Cytochromes P450 1A1 and 1A2, Thereby Modulating Its Own Metabolism

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