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- W2758470441 abstract "Reactive metabolites (RM) formed from bioactivation of drugs can covalently modify liver proteins and cause mechanism-based inactivation of major cytochrome P450 (CYP450) enzymes. Risk of bioactivation of a test compound is routinely examined as part of lead optimization efforts in drug discovery. Here we described a chemoproteomic platform to assess in vitro and in vivo bioactivation potential of drugs. This platform enabled us to determine reactivity of thousands of proteomic cysteines toward RMs of diclofenac formed in human liver microsomes and living animals. We pinpointed numerous reactive cysteines as the targets of RMs of diclofenac, including the active (heme-binding) sites on several key CYP450 isoforms (1A2, 2E1 and 3A4 for human, 2C39 and 3A11 for mouse). This general platform should be applied to other drugs, drug candidates, and xenobiotics with potential hepatoxicity, including environmental organic substances, bioactive natural products, and traditional Chinese medicine." @default.
- W2758470441 created "2017-10-06" @default.
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- W2758470441 date "2017-10-06" @default.
- W2758470441 modified "2023-10-14" @default.
- W2758470441 title "A Chemoproteomic Platform To Assess Bioactivation Potential of Drugs" @default.
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- W2758470441 doi "https://doi.org/10.1021/acs.chemrestox.7b00183" @default.
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