Title : Retigabine N-glucuronidation and its potential role in enterohepatic circulation.

Pub. Date : 1999 May

PMID : 10220490






2 Functional Relationships(s)
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1 From the known substrate specificities of UGT1A4 toward lamotrigine and bilirubin and our activity and inhibition data, we conclude that UGT1A4 is a major retigabine N-glucuronosyl transferase in vivo and significantly contributes to the enterohepatic cycling of the drug. Lamotrigine UDP glucuronosyltransferase family 1 member A4 Homo sapiens
2 From the known substrate specificities of UGT1A4 toward lamotrigine and bilirubin and our activity and inhibition data, we conclude that UGT1A4 is a major retigabine N-glucuronosyl transferase in vivo and significantly contributes to the enterohepatic cycling of the drug. Lamotrigine UDP glucuronosyltransferase family 1 member A4 Homo sapiens