Title : Characterization of rat and human UDP-glucuronosyltransferases responsible for the in vitro glucuronidation of diclofenac.

Pub. Date : 2001 May

PMID : 11294973






3 Functional Relationships(s)
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1 Conversely, human UGT2B7 displayed a high rate of diclofenac glucuronide formation (>500 pmol/min/mg protein). 1-O-(2-((2',6'-dichlorophenyl)amino)phenylacetyl)glucopyranuronic acid UDP glucuronosyltransferase family 2 member B7 Homo sapiens
2 Morphine is a known substrate for rat UGT2B1 and human UGT2B7 and both total morphine glucuronidation (3-O- and 6-O-glucuronides) and diclofenac glucuronidation reactions showed a strong correlation with one another in human liver microsome samples. Morphine UDP glucuronosyltransferase family 2 member B7 Homo sapiens
3 These data suggested that rat UGT2B1 and human UGT2B7 were the major UGT isoforms involved in the glucuronidation of diclofenac. Diclofenac UDP glucuronosyltransferase family 2 member B7 Homo sapiens