Results 151 to 160 of about 42,320 (201)
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Hydrolysis of Morphine Glucuronide

Journal of Forensic Sciences, 1974
Abstract In procedures requiring the quantitative analysis for total morphine in body fluids there is a need to liberate the bound drug, and for the hydrolysis of conjugates in urine there are alternative methods of acid or enzyme hydrolysis.
F, Fish, T S, Hayes
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Glucuronidation in fish

Aquatic Toxicology, 1991
Douglas J Clarke   +2 more
exaly   +2 more sources

Glucuronidation

2021
Glucuronidation catalyzed by uridine 5′-diphospho-glucuronosyltransferase (UGT) is the most common phase II metabolism. The UGTs can severely limit a drug's exposure and generate reactive metabolites, leading to toxicity. This chapter provides a brief overview of the current understanding of the UGT enzyme family, followed by various medicinal ...
openaire   +1 more source

Intermediates for Glucuronide Synthesis: 7-Hydroxycoumarin Glucuronide

Journal of Chemical Research, 1997
A convenient synthesis of the important metabolite 7-hydroxycoumarin glucuronide 3 is presented, including a first report of the β-imidate 11β, together with new preparations of the iodosugar 6 and α-imidate 11α: stability data on 11α and 11β are also given, and the importance of carefully controlled hydrolysis in the last step of the preparation of 3 ...
Richard T. Brown   +2 more
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On the formation of carbamate glucuronides

Xenobiotica, 1990
(1990). On the formation of carbamate glucuronides. Xenobiotica: Vol. 20, No. 1, pp. 133-134.
L P, Delbressine   +3 more
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Drug glucuronidation in humans

Pharmacology & Therapeutics, 1991
Glucuronidation is a major metabolic pathway for a large number of drugs in humans. Conjugation of drugs and other chemicals with glucuronic acid is catalyzed by the multigene UDP-glucuronosyltransferase family. It is believed that a number (unspecified at present) of glucuronosyltransferase isozymes, which probably differ in terms of substrate ...
J O, Miners, P I, Mackenzie
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Uptake of Glucuronides into Isolated Hepatocytes and their Effects on Glucuronide and Sulphate Conjugation

Acta Pharmacologica et Toxicologica, 1978
Abstract Uptake studies, using radioactive labelled glucuronides, have demonstrated the ability of 4‐nitrophenyl glucuronide and phenolphthalein glucuronide to enter isolated rat hepatocytes. Of these glucuronides 4‐nitrophenyl glucuronide was distributed in a similar manner to O‐methylglucose, whereas phenolphthalein glucuronide was bound to cellular ...
A, Norling   +3 more
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The Effect of Chloroform Inhalation on Hepatic Glucuronidation and De-Glucuronidation Mechanisms

Drug and Chemical Toxicology, 1980
The effect of 2, 4, 6 or 8 exposures to chloroform vapour on hepatic glucuronidating (UDPGA transferase) and de-glucuronidating (beta-glucuronidase) levels has been studied in rats. Successive treatments progressively decreased hepatic UDPGA transferase to a minimum of 53% of the control level.
I D, Capel   +3 more
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Microsomal Acyl Glucuronidation: Enzyme-Kinetic Studies with Labile Glucuronides

Pharmacology, 2008
Because of the labile nature of acyl glucuronides under physiologic conditions, metabolic rates of formation calculated using traditional methods may be confounded by concomitant rates of degradation. True metabolic formation rates may be approximated by stabilization of the metabolic product or by purifying the metabolite and calculating its ...
H, Spahn-Langguth, L Z, Benet
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Scintigraphic imaging with a peptide glucuronide in rabbits: 99mTc- exorphin C glucuronide

Applied Radiation and Isotopes, 2007
A peptide glucuronide (Exorphin C glucuronide) was labeled with 99mTc using glucoheptonate (GH) as a bifunctional chelating agent. Scintigraphic imaging was performed in male Albino rabbits. Exorphin C glucuronide showed rapid and efficient labeling with 99mTc using glucoheptonate as a bifunctional chelate.
Ertay T.   +5 more
openaire   +5 more sources

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