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 …

[HTML][HTML] Current trends in drug metabolism and pharmacokinetics

Y Li, Q Meng, M Yang, D Liu, X Hou, L Tang… - … Pharmaceutica Sinica B, 2019 - Elsevier
Pharmacokinetics (PK) is the study of the absorption, distribution, metabolism, and excretion
(ADME) processes of a drug. Understanding PK properties is essential for drug development …

A comprehensive review of UDP-glucuronosyltransferase and esterases for drug development

S Oda, T Fukami, T Yokoi, M Nakajima - Drug metabolism and …, 2015 - Elsevier
UDP-glucuronosyltransferase (UGT) and esterases are recognized as the most important
non-P450 enzymes because of their high contribution to drug metabolism. UGTs catalyze …

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 …

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 …

Evidence-based strategies for the characterisation of human drug and chemical glucuronidation in vitro and UDP-glucuronosyltransferase reaction phenotyping

JO Miners, A Rowland, JJ Novak, K Lapham… - Pharmacology & …, 2021 - Elsevier
Enzymes of the UDP-glucuronosyltransferase (UGT) superfamily contribute to the
elimination of drugs from almost all therapeutic classes. Awareness of the importance of …

Functions and transcriptional regulation of adult human hepatic UDP-glucuronosyl-transferases (UGTs): mechanisms responsible for interindividual variation of UGT …

KW Bock - Biochemical pharmacology, 2010 - Elsevier
Ten out of 19 UDP-glucuronosyltransferases (UGTs) are substantially expressed in adult
human liver (> 1% of total UGTs); 5 UGT1 isoforms (UGT1A1, 1A3, 1A4, 1A6 and 1A9) and 5 …

Regulation of human UDP-glycosyltransferase (UGT) genes by miRNAs

DG Hu, PI Mackenzie, JA Hulin… - Drug metabolism …, 2022 - Taylor & Francis
The human UGT gene superfamily is divided into four subfamilies (UGT1, UGT2, UGT3 and
UGT8) that encodes 22 functional enzymes. UGTs are critical for the metabolism and …

The ontogeny of UDP-glucuronosyltransferase enzymes, recommendations for future profiling studies and application through physiologically based pharmacokinetic …

J Badée, S Fowler, SN de Wildt, AC Collier… - Clinical …, 2019 - Springer
Limited understanding of drug pharmacokinetics in children is one of the major challenges
in paediatric drug development. This is most critical in neonates and infants owing to rapid …