Selectivity for inhibition of nilotinib on the catalytic activity of human UDP-glucuronosyltransferases-Reference-Cited by-同舟云学术

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Selectivity for inhibition of nilotinib on the catalytic activity of human UDP-glucuronosyltransferases

Published:2013-09-25 Issue:4 Volume:44 Page:320-325
ISSN:0049-8254
Container-title:Xenobiotica
language:en
Short-container-title:Xenobiotica

Author:

Ai Limei,Zhu Liangliang,Yang Lu,Ge Guangbo,Cao Yunfeng,Liu Yong,Fang Zhongze,Zhang Yanyan

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/00498254.2013.840750

Reference20 articles.

1. EVALUATION OF 3′-AZIDO-3′-DEOXYTHYMIDINE, MORPHINE, AND CODEINE AS PROBE SUBSTRATES FOR UDP-GLUCURONOSYLTRANSFERASE 2B7 (UGT2B7) IN HUMAN LIVER MICROSOMES: SPECIFICITY AND INFLUENCE OF THE UGT2B7*2 POLYMORPHISM

2. Interindividual variability in hepatic drug glucuronidation: studies into the role of age, sex, enzyme inducers, and genetic polymorphism using the human liver bank as a model system

3. The small-molecule tyrosine kinase inhibitor nilotinib is a potent noncompetitive inhibitor of the SN-38 glucuronidation by human UGT1A1

4. Quantitative Analysis of UDP-Glucuronosyltransferase (UGT) 1A and UGT2B Expression Levels in Human Livers

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2. Human UDP-glucuronosyltransferase 1As catalyze aristolochic acid D O-glucuronidation to form a lesser nephrotoxic glucuronide;Journal of Ethnopharmacology;2024-06

3. Avapritinib Carries the Risk of Drug Interaction via Inhibition of UDP-Glucuronyltransferase (UGT) 1A1;Current Drug Metabolism;2024-03

4. Detection of uridine diphosphate glucuronosyltransferase 1A1 for pancreatic cancer imaging and treatment via a “turn-on” fluorescent probe;The Analyst;2024

5. Characterization of the glucuronidating pathway of pectolinarigenin, the major active constituent of the Chinese medicine Daji, in humans and its influence on biological activities;Journal of Ethnopharmacology;2024-01

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