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Isolation from rat urine and human liver microsomes and identification by electrospray and nanospray tandem mass spectrometry of new malagashanine metabolites
被引:0
|作者:
Rafatro, H
Verbeeck, RK
Gougnard, TYR
De Jonghe, PJM
Rasoanaivo, P
Laurent, A
Lhoëst, G
机构:
[1] Catholic Univ Louvain, Dept Pharmaceut Sci, Pharmacokinet Drug Metab Nutr & Toxicol Unit, PMNT,Lab Mass Spectrometry, B-1200 Brussels, Belgium
[2] Univ Antananarivo, Fac Sci, Lab Pharmacol Gen & Pharmacocinet, Antananarivo, Madagascar
[3] CHU Liege, Lab Clin Toxicol, B-4000 Liege, Belgium
[4] Natl Inst Publ Hlth & Environm, Analyt Chem Lab, NL-3720 BA Bilthoven, Netherlands
[5] Inst Malgache Rech Appl, Dept Phytochim Pharmacol, Antananarivo, Madagascar
来源:
关键词:
malagashanine metabolism;
dihydroindole alkaloids;
Strychnos;
mass spectrometry;
high-performance liquid chromatography;
D O I:
10.1002/1096-9888(200009)35:9<1112::AID-JMS39>3.0.CO;2-K
中图分类号:
Q5 [生物化学];
学科分类号:
071010 ;
081704 ;
摘要:
Malagashanine has been isolated from indigenous madagasean Strychnos myrtoides alkaloids used traditionally to treat malaria, This alkaloid was found to enhance the action of chloroquine against chloroquine-resistant strains of Plasmodium falciparum when combined with classical antimalarial drugs (chloroquine, quinine), The present study was carried out in order to investigate by electrospray mass and tandem mass spectrometry and NMR spectroscopy the structure of two new metabolites isolated from rat urine and human liver microsomes, We were able to demonstrate the presence of two new metabolites of malagashanine corresponding to a malagashanine N-demethylated metabolite and to the oxidation of malagashanine in the alpha-position of the N-methyl group to produce a carbinolamine function. The latter metabolite may be subject to ring and open-chain tautomerism effects and dimeric species were detected in the electrospray mass spectrum. Copyright (C) 2000 John Wiley & Sons, Ltd.
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页码:1112 / 1120
页数:9
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