Synthesis of urine drug metabolites:: glucuronic acid glycosides of phenol intermediates

被引:14
作者
Arewang, Carl Johan
Lahmann, Martina
Oscarson, Stefan
Tiden, Anna-Karin [1 ]
机构
[1] AstraZeneca, R&D Sodertalje, Dept Chem, S-15185 Sodertalje, Sweden
[2] Univ Stockholm, Arrhenius Lab, Dept Organ Chem, S-10691 Stockholm, Sweden
关键词
metabolites; glycosylation; glucuronic acid donor; phenolic glucuronide;
D O I
10.1016/j.carres.2007.01.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The investigation of drug metabolism requires substantial amount of metabolites. Isolation from urine is tedious, therefore, the material obtained by synthesis is preferred. Substantial amounts of three tentative drug metabolites, phenolic glucuronides, have been prepared using easily available glycosyl donors. The final products [3(2-N-methyl-N-isopropylaminoethoxy)phenyl] beta-D-glucopyranosiduronic acid, 4-amino-3,5-dimethylphenyl beta-D-glucopyranosiduronic acid and [2(S)-propanoyl-6-O-naphthyl] beta-D-glucopyranuronic acid are useful as, for example, reference material in metabolite investigations. (c) 2007 Published by Elsevier Ltd.
引用
收藏
页码:970 / 974
页数:5
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