Understanding Cooperativity in Human P450 Mediated Drug-Drug Interactions
Author:
Publisher
Informa UK Limited
Subject
Pharmacology (medical),General Pharmacology, Toxicology and Pharmaceutics
Link
http://www.tandfonline.com/doi/pdf/10.1080/03602530701498521
Reference45 articles.
1. THE HEMOGLOBIN SYSTEM
2. NON-MICHAELIS-MENTEN KINETICS IN CYTOCHROME P450-CATALYZED REACTIONS
3. Current views on the fundamental mechanisms of cytochrome P450 allosterism
4. Is There a Toxicological Advantage for Non-hyperbolic Kinetics in Cytochrome P450 Catalysis?
5. Homotropic cooperativity of monomeric cytochrome P450 3A4 in a nanoscale native bilayer environment
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1. Synthesis, single crystal investigations, and quantum computational investigation of a new 1,1′-(3,5-dhydroxy-3-methyl-2′-nitro-1,2,3,4-tetrahydro-[1,1′-biphenyl]-2,6-diyl)bis(ethan-1-one) as a potent inhibitor for Cytochrome P450 3A4;Journal of Molecular Structure;2024-11
2. Combining Small-Molecule Bioconjugation and Hydrogen–Deuterium Exchange Mass Spectrometry (HDX-MS) to Expose Allostery: the Case of Human Cytochrome P450 3A4;ACS Chemical Biology;2021-04-29
3. Homotropic Cooperativity of Midazolam Metabolism by Cytochrome P450 3A4: Insight from Computational Studies;Journal of Chemical Information and Modeling;2021-04-22
4. Combining small-molecule bioconjugation and hydrogen-deuterium exchange mass spectrometry (HDX-MS) to expose allostery: the case of human cytochrome P450 3A4;2020-06-11
5. Drug–Drug Interactions between Atorvastatin and Dronedarone Mediated by Monomeric CYP3A4;Biochemistry;2017-12-14
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