نتایج جستجو برای: glucuronosyltransferase

تعداد نتایج: 2005  

Journal: :Drug metabolism and disposition: the biological fate of chemicals 1999
K W Ward L M Azzarano W E Bondinell R D Cousins W F Huffman D R Jakas R M Keenan T W Ku D Lundberg W H Miller J A Mumaw K A Newlander J L Pirhalla T J Roethke K L Salyers P R Souder G J Stelman B R Smith

Allometric scaling may be used in drug development to predict the pharmacokinetics of xenobiotics in humans from animal data. Although allometry may be successful for compounds that are excreted unchanged or that are oxidatively metabolized (with corrections for metabolic capacity), it has been more challenging for compounds excreted primarily as conjugates in bile. (S)-10, 11-Dihydro-3-[3-(pyr...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2004
Yuji Ishii Aya Miyoshi Daisuke Maji Hideyuki Yamada Kazuta Oguri

Our previous study suggested that hetero-oligomer formation of guinea pig liver UDP-glucuronosyltransferases (UGTs) 2B21 and 2B22 enhances UGT2B21-catalyzed morphine-6-glucuronidation. In this work, further evidence for a functional hetero-oligomer between UGT2B21 and UGT2B22 was provided by studies of the glucuronidation of chloramphenicol with dual expression in COS-7 cells. UGT2B21 expressed...

2017
Jun Jiang Hua-Gui Wang Wei-Li Wu Xiang-Xin Peng

IntRoductIon Gilbert syndrome (GS, MIM #143500) is characterized by fluctuating mild, unconjugated hyperbilirubinemia <85 μmol/L and is caused by mutations in the bilirubin uridine diphosphate (UDP)‐glucuronosyltransferase gene (UGT1A1).[1] Dubin‐Johnson syndrome (DJS, MIM #237500) is characterized by fluctuating mild, predominantly conjugated hyperbilirubinemia and is caused by mutations in th...

Journal: :Drug metabolism and disposition: the biological fate of chemicals 2004
Peter G Wells Peter I Mackenzie Jayanta Roy Chowdhury Chantal Guillemette Philip A Gregory Yuji Ishii Antony J Hansen Fay K Kessler Perry M Kim Namita Roy Chowdhury Joseph K Ritter

This article is an updated report of a symposium held at the June 2000 annual meeting of the American Society for Pharmacology and Experimental Therapeutics in Boston. The symposium was sponsored by the ASPET Divisions for Drug Metabolism and Molecular Pharmacology. The report covers research from the authors' laboratories on the structure and regulation of UDP-glucuronosyltransferase (UGT) gen...

2013
Kyohei Sumida Makiko Kawana Emi Kouno Tomoo Itoh Shuhei Takano Tomoya Narawa Robert H. Tukey Ryoichi Fujiwara

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