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dc.contributor.authorUchaipichat, Verawan Nu
dc.contributor.authorMackenzie, Peter Ian
dc.contributor.authorElliot, David John
dc.contributor.authorMiners, John Oliver
dc.date.accessioned2010-07-27T06:22:27Z
dc.date.available2010-07-27T06:22:27Z
dc.date.issued2006en_US
dc.identifier.citationUchaipichat, V.N., Mackenzie, P.I., Elliot, D.J., & Miners, J.O., 2006. Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) 'probes' for human UDP-glucuronosyltransferases. Drug Metabolism and Disposition, 34(3), 449-456.en
dc.identifier.issn0090-9556en_US
dc.identifier.urihttp://hdl.handle.net/2328/11384
dc.titleSelectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) 'probes' for human UDP-glucuronosyltransferasesen_US
dc.typeArticleen_US
dc.identifier.rmid2006003098en_US
dc.identifier.doihttps://doi.org/10.1124/dmd.105.007369en
dc.subject.forgroup1115 Pharmacology and Pharmaceutical Sciencesen_US


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