Planta Med 2003; 69(4): 380-382
DOI: 10.1055/s-2003-38881
Letter
© Georg Thieme Verlag Stuttgart · New York

Glucosinolates in Moringa stenopetala

Yalemtsehay Mekonnen1 , Birgit Dräger1
  • 1Institute of Pharmaceutical Biology, Martin-Luther-Universität Halle-Wittenberg, Halle/Saale, Germany
Weitere Informationen

Publikationsverlauf

Received: August 28, 2002

Accepted: December 15, 2002

Publikationsdatum:
23. April 2003 (online)

Abstract

Bio-guided fractionation of seed extracts from Moringa stenopetala resulted in a myrosinase hydrolysis product, 5,5-dimethyloxazolidine-2-thione. It is formed from the glucosinolate glucoconringiin, which was identified together with O-(rhamnopyranosyloxy)benzyl glucosinolate from M. stenopetala for the first time. The glucosinolates in seeds, leaves and roots of M. stenopetala were quantified as des-sulphoglucosinolate by HPLC. The seeds without testa contained the highest concentration of glucoconringiin and of O-(rhamnopyranosyloxy)benzyl glucosinolate within the plant, 3 % and 19 % of dry mass, respectively.

Abbreviations

GLS:glucosinolate

GC:glucoconringiin

RB-GLS:O-(rhamnopyranosyloxy)benzyl glucosinolate

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Dr. Birgit Dräger

Institute of Pharmaceutical Biology

Martin-Luther-Universität Halle-Wittenberg

Hoher Weg 8

06120 Halle/Saale

Germany

Telefon: +49-3455525765

Fax: +49-3455525021

eMail: Draeger@pharmazie.uni-halle.de