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2. The prediction of drug-glucuronidation parameters in humans: UDP-glucuronosyltransferase enzyme-selective substrate and inhibitor probes for reaction phenotyping and in vitro-in vivo extrapolation of drug clearance and drug-drug interaction potential. Miners JO, Mackenzie PI, Knights KM. Drug Metab Rev; 2010 Feb; 42(1):196-208. PubMed ID: 19795925 [Abstract] [Full Text] [Related]
4. Glucuronidation of amine substrates by purified and expressed UDP-glucuronosyltransferase proteins. Green MD, Tephly TR. Drug Metab Dispos; 1998 Sep; 26(9):860-7. PubMed ID: 9733664 [Abstract] [Full Text] [Related]
5. Regio- and stereospecific N-glucuronidation of medetomidine: the differences between UDP glucuronosyltransferase (UGT) 1A4 and UGT2B10 account for the complex kinetics of human liver microsomes. Kaivosaari S, Toivonen P, Aitio O, Sipilä J, Koskinen M, Salonen JS, Finel M. Drug Metab Dispos; 2008 Aug; 36(8):1529-37. PubMed ID: 18474681 [Abstract] [Full Text] [Related]
6. Glucuronidation of amines and other xenobiotics catalyzed by expressed human UDP-glucuronosyltransferase 1A3. Green MD, King CD, Mojarrabi B, Mackenzie PI, Tephly TR. Drug Metab Dispos; 1998 Jun; 26(6):507-12. PubMed ID: 9616184 [Abstract] [Full Text] [Related]
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12. Glucuronidation of opioids, carboxylic acid-containing drugs, and hydroxylated xenobiotics catalyzed by expressed monkey UDP-glucuronosyltransferase 2B9 protein. Green MD, Bélanger G, Hum DW, Bélanger A, Tephly TR. Drug Metab Dispos; 1997 Dec; 25(12):1389-94. PubMed ID: 9394029 [Abstract] [Full Text] [Related]
15. N-glucuronidation of the platelet-derived growth factor receptor tyrosine kinase inhibitor 6,7-(dimethoxy-2,4-dihydroindeno[1,2-C]pyrazol-3-yl)-(3-fluoro-phenyl)-amine by human UDP-glucuronosyltransferases. Yan Z, Caldwell GW, Gauthier D, Leo GC, Mei J, Ho CY, Jones WJ, Masucci JA, Tuman RW, Galemmo RA, Johnson DL. Drug Metab Dispos; 2006 May; 34(5):748-55. PubMed ID: 16455802 [Abstract] [Full Text] [Related]