Title : Use of Phenotypically Poor Metabolizer Individual Donor Human Liver Microsomes To Identify Selective Substrates of UGT2B10.

Pub. Date : 2020 Mar

PMID : 31839590






1 Functional Relationships(s)
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1 Of these, dothiepin, cidoxepin, cyclobenzaprine, azatadine, cyproheptadine, bifonazole, and asenapine were indicated to be selective UGT2B10 substrates which have not previously been described. asenapine UDP glucuronosyltransferase family 2 member B10 Homo sapiens