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Metabolism of a new neuroprotective agent for ischemia-reperfusion damage, KR-31543 in the rat using liquid chromatography/electrospray mass spectrometry.

作者信息

Kim John, Ji Hye Young, Lee Seung-Seok, Yoo Sung-Eun, Kim Sun Ok, Lee Dong Ha, Lim Hong, Lee Hye Suk

机构信息

Faculty of Pharmaceutical Sciences, University of British Columbia, Vancouver, Canada.

出版信息

Arch Pharm Res. 2002 Oct;25(5):664-8. doi: 10.1007/BF02976941.

Abstract

KR-31543, (2S,3R,4S)-6-amino-4-[N-(4-chlorophenyl)-N-(2-methyl-2H-tetrazol-5-ylmethyl)amino]-3,4-dihydro-2-dimethoxymethyl-3-hydroxy-2-methyl-2H-1-benzopyran is a new neuroprotective agent for ischemia-reperfusion damage. The in vitro and in vivo metabolism of KR-31543 in rats has been studied by LC-electrospray mass spectrometry. Rat liver microsomal incubation of KR-31543 in the presence of NADPH resulted in the formation of a metabolite M1. M1 was identified as N-(4-chlorophenyl)-N-(2-methyl-2H-tetrazol-5-ylmethyl)amine on the basis of LC-MS/MS analysis with the synthesized authentic standard. Rat CYP3A1 and 3A2 are the major CYP isozymes involved in the formation of M1.

摘要

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