Title : Diclofenac-induced liver injury: a paradigm of idiosyncratic drug toxicity.

Pub. Date : 2003 Nov 1

PMID : 14575648






3 Functional Relationships(s)
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Compound Name
Protein Name
Organism
1 Among these are metabolic factors (bioactivation by hCYP2C9 or hCYP3A4 to thiol-reactive quinone imines, activation by hUGT2B7 to protein-reactive acyl glucuronides and iso-glucuronides, and 4"-hydroxylation secondary to diclofenac glucuronidation), as well as kinetic factors (Mrp2-mediated concentrative transport of diclofenac metabolites into bile). Glucuronides UDP glucuronosyltransferase family 2 member B7 Homo sapiens
2 Among these are metabolic factors (bioactivation by hCYP2C9 or hCYP3A4 to thiol-reactive quinone imines, activation by hUGT2B7 to protein-reactive acyl glucuronides and iso-glucuronides, and 4"-hydroxylation secondary to diclofenac glucuronidation), as well as kinetic factors (Mrp2-mediated concentrative transport of diclofenac metabolites into bile). diclofenac glucuronidation UDP glucuronosyltransferase family 2 member B7 Homo sapiens
3 Among these are metabolic factors (bioactivation by hCYP2C9 or hCYP3A4 to thiol-reactive quinone imines, activation by hUGT2B7 to protein-reactive acyl glucuronides and iso-glucuronides, and 4"-hydroxylation secondary to diclofenac glucuronidation), as well as kinetic factors (Mrp2-mediated concentrative transport of diclofenac metabolites into bile). Diclofenac UDP glucuronosyltransferase family 2 member B7 Homo sapiens