The UDP-glycosyltransferase (UGT) superfamily: new members, new functions, and novel paradigms

R Meech, DG Hu, RA McKinnon… - Physiological …, 2019 - journals.physiology.org
UDP-glycosyltransferases (UGTs) catalyze the covalent addition of sugars to a broad range
of lipophilic molecules. This biotransformation plays a critical role in elimination of a broad …

The prediction of drug-glucuronidation parameters in humans: UDP-glucuronosyltransferase enzyme-selective substrate and inhibitor probes for reaction phenotyping …

JO Miners, PI Mackenzie, KM Knights - Drug metabolism reviews, 2010 - Taylor & Francis
Major advances in the characterization of uridine diphosphate (UDP)-
glucuronosyltransferase (UGT) enzyme substrate and inhibitor selectivities and the …

Simultaneous absolute protein quantification of transporters, cytochromes P450, and UDP-glucuronosyltransferases as a novel approach for the characterization of …

S Ohtsuki, O Schaefer, H Kawakami, T Inoue… - Drug metabolism and …, 2012 - ASPET
The purpose of the present study was to determine the absolute protein expression levels of
multiple drug-metabolizing enzymes and transporters in 17 human liver biopsies, and to …

Metabolic profiles of propofol and fospropofol: clinical and forensic interpretative aspects

RJ Dinis-Oliveira - BioMed research international, 2018 - Wiley Online Library
Propofol is an intravenous short‐acting anesthetic widely used to induce and maintain
general anesthesia and to provide procedural sedation. The potential for propofol …

Optimized assays for human UDP-glucuronosyltransferase (UGT) activities: altered alamethicin concentration and utility to screen for UGT inhibitors

RL Walsky, JN Bauman, K Bourcier, G Giddens… - Drug Metabolism and …, 2012 - ASPET
The measurement of the effect of new chemical entities on human UDP-
glucuronosyltransferase (UGT) marker activities using in vitro experimentation represents an …

Transcriptional regulation of human UDP-glucuronosyltransferase genes

DG Hu, R Meech, RA McKinnon… - Drug metabolism …, 2014 - Taylor & Francis
Glucuronidation is an important metabolic pathway for many small endogenous and
exogenous lipophilic compounds, including bilirubin, steroid hormones, bile acids …

Quantitative distribution of mRNAs encoding the 19 human UDP-glucuronosyltransferase enzymes in 26 adult and 3 fetal tissues

MH Court, X Zhang, X Ding, KK Yee, LM Hesse… - Xenobiotica, 2012 - Taylor & Francis
The purpose of this study was to generate, by real-time PCR, a quantitative expression level
profile of the 19 human UDP-glucuronosyltransferases (UGTs) of subfamilies 1A, 2A and 2B …

UGT genomic diversity: beyond gene duplication

C Guillemette, E Lévesque, M Harvey… - Drug metabolism …, 2010 - Taylor & Francis
The human uridine diphospho (UDP)-glucuronosyltransferase (UGT) superfamily comprises
enzymes responsible for a major biotransformation phase II pathway: the glucuronidation …

N-glucuronidation of drugs and other xenobiotics by human and animal UDP-glucuronosyltransferases

S Kaivosaari, M Finel, M Koskinen - Xenobiotica, 2011 - Taylor & Francis
Metabolic disposition of drugs and other xenobiotics includes glucuronidation reactions that
are catalyzed by the uridine diphosphate glucuronosyltransferases (UGTs). The most …

Reaction phenotyping: advances in the experimental strategies used to characterize the contribution of drug-metabolizing enzymes

MA Zientek, K Youdim - Drug Metabolism and Disposition, 2015 - ASPET
During the process of drug discovery, the pharmaceutical industry is faced with numerous
challenges. One challenge is the successful prediction of the major routes of human …