Inhibition of human UDP‐glucuronosyltransferase enzymes by midostaurin and ruxolitinib: implications for drug–drug interactions
Author:
Affiliation:
1. School of Life and Pharmaceutical SciencesDalian University of Technology Panjin 124221 China
2. Department of Occupational and Environmental HealthDalian Medical University Dalian 116044 China
Funder
National Basic Research Program of China
Publisher
Wiley
Subject
Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/bdd.2241
Reference41 articles.
1. Selectivity for inhibition of nilotinib on the catalytic activity of human UDP-glucuronosyltransferases
2. Effect of Aging on Glucuronidation of Valproic Acid in Human Liver Microsomes and the Role of UDP-Glucuronosyltransferase UGT1A4, UGT1A8, and UGT1A10
3. IC50-to-Ki: a web-based tool for converting IC50 to Ki values for inhibitors of enzyme activity and ligand binding
4. Comparison of the inhibition potentials of icotinib and erlotinib against human UDP-glucuronosyltransferase 1A1
5. Investigation into CYP3A4-mediated drug–drug interactions on midostaurin in healthy volunteers
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