Affiliation:
1. Biochemical Laboratory, Division of Organic Chemistry, Tokyo College of Pharmacy, Ueno-sakuragi, Taito-ku, Tokyo 110, Japan
Abstract
Abstract
Six metabolites of quinine were detected in the urine of rabbits given its monohydrochloride orally. Of the metabolites detected, three major ones were quantitatively separated and characterized as 2′-hydroxyquinine, 2′,3-dihydroxyquinine, and 2′,6′-dihydroxycinchonidine. No unchanged alkaloid was detected in the urine. The present results indicate that the most important reaction in the metabolism of the alkaloid in the rabbit is the formation of 2′-carbostyril derivatives.
Publisher
Oxford University Press (OUP)
Subject
Pharmaceutical Science,Pharmacology
Cited by
12 articles.
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1. TheCinchonaGroup;Chemistry of Heterocyclic Compounds: A Series Of Monographs;2008-01-02
2. Bibliography;Handbook of Biotransformations of Aromatic Compounds;2004-11-10
3. 3.14 Alkaloids;Analytical Toxicology for Clinical, Forensic and Pharmaceutical Chemists;1997-12-31
4. Characterization of the principal metabolite of quinine in human urine by1H-n.m.r. spectroscopy;Xenobiotica;1991-01
5. The Disposition of Quinine in the Rat Isolated Perfused Liver: Effect of Dose Size;Journal of Pharmacy and Pharmacology;1990-01