Results 1 to 10 of about 55,992 (193)

Glucuronidation by UGT1A1 is the dominant pathway of the metabolic disposition of belinostat in liver cancer patients. [PDF]

open access: yesPLoS ONE, 2013
UnlabelledBelinostat is a hydroxamate class HDAC inhibitor that has demonstrated activity in peripheral T-cell lymphoma and is undergoing clinical trials for non-hematologic malignancies.
Ling-Zhi Wang   +16 more
doaj   +7 more sources

Systematic characterization of lysine glucuronidation in a bispecific antibody [PDF]

open access: yesmAbs
This study presents a systematic characterization of lysine glucuronidation that was revealed during the charge variant characterization of a bispecific antibody (bsAb).
Michael R. Reyda   +7 more
doaj   +2 more sources

Dysregulated hepatic UDP-glucuronosyltransferases and flavonoids glucuronidation in experimental colitis

open access: yesFrontiers in Pharmacology, 2022
Glucuronidation catalyzed by UDP-glucuronosyltransferases (UGTs) is one of the most important phase II mechanisms, facilitating drug clearance via conjugation of glucuronic acid with polar groups of xenobiotics.
Wanying Zeng   +9 more
doaj   +1 more source

Variation in trans-3'-hydroxycotinine glucuronidation does not alter the nicotine metabolite ratio or nicotine intake. [PDF]

open access: yesPLoS ONE, 2013
CYP2A6 metabolizes nicotine to its primary metabolite cotinine and also mediates the metabolism of cotinine to trans-3'-hydroxycotinine (3HC). The ratio of 3HC to cotinine (the "nicotine metabolite ratio", NMR) is an in vivo marker for the rate of CYP2A6
Andy Z X Zhu   +5 more
doaj   +1 more source

Ethyl glucuronide [PDF]

open access: yesAnnals of Clinical Biochemistry: International Journal of Laboratory Medicine, 2012
Alcohol is associated with significant morbidity and mortality. Subjects abusing alcohol can be identified through clinical history, examination or self-report questionnaires. A range of biomarkers is available for detecting alcohol misuse, but there is still a need for a marker that can detect alcohol consumption in the time window between one day ...
Walsham, Natalie E., Sherwood, Roy
openaire   +3 more sources

UGT1A1 and UGT1A9 Are Responsible for Phase II Metabolism of Tectorigenin and Irigenin In Vitro

open access: yesMolecules, 2022
Tectorigenin and irigenin are biologically active isoflavones of Belamcanda chinensis (L.) DC. Previous studies indicated that both compounds could be metabolized in vivo; however, the kinetic parameters of enzymes involved in the metabolization of ...
Ji Li, Zhangyao Xu, Jifeng Gu
doaj   +1 more source

Potential Assessment of UGT2B17 Inhibition by Salicylic Acid in Human Supersomes In Vitro

open access: yesMolecules, 2021
Glucuronidation is a Phase 2 metabolic pathway responsible for the metabolism and excretion of testosterone to a conjugate testosterone glucuronide.
Hassan Salhab   +2 more
doaj   +1 more source

Profiling of Urinary Glucuronidated Bile Acids across Age Groups

open access: yesMetabolites, 2022
We investigated the age-dependent changes in urinary excretion of glucuronidated bile acids at the C-3 position. Bile acid 3-glucuronides accounted for 0.5% of urinary bile acids in neonates, and the proportion of bile acid 3-glucuronides plateaued at 1 ...
Yamato Muto   +6 more
doaj   +1 more source

Glucuronidation Pathways of 5- and 7-Hydroxypropranolol: Determination of Glucuronide Structures and Enzyme Selectivity

open access: yesMolecules, 2023
Propranolol, a non-selective beta-blocker medication, has been utilized in the treatment of cardiovascular diseases for several decades. Its hydroxynaphthyl metabolites have been recognized to possess varying degrees of beta-blocker activity due to the ...
Fan Yang   +3 more
doaj   +1 more source

Identification of naturally occurring inhibitors in Xian-Ling-Gu-Bao capsule against the glucuronidation of estrogens

open access: yesFrontiers in Pharmacology, 2022
Xian-Ling-Gu-Bao (XLGB) capsule, a well-known traditional Chinese medicine prescription, is widely used for the treatment of osteoporosis. It could significantly increase the levels of estrogen in ovariectomized rats and mice.
Liangliang He   +13 more
doaj   +1 more source

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