Planta Med 1983; 48(7): 136-141
DOI: 10.1055/s-2007-969908
Research Articles

© Hippokrates Verlag Stuttgart

Chemistry, 13C-NMR Study and Pharmacology of Two Saponins from Colubrina asiatica

H. Wagner1 , S. Ott[3] 1 , K. Jurcic1 , J. Morton[4] , A. Neszmelyi2
  • 1Institut für Pharmazeutische Biologie der Universität München
  • 2Central Research Institute for Chemistry of the Hungarian Academy of Science, Budapest
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Publikationsverlauf

1983

1983

Publikationsdatum:
26. März 2007 (online)

Abstract

From the leaves of Colubrina asiatica BRONGEN (Rhamnaceae) two saponins have been isolated and structurally elucidated, mainly by 13C-NMR-spectroscopic methods, as jujubogenin-3-O-[2-O-acetyl-3-O-(3-O-β-D-xylopyranosyl-4-O-acetyl-β-D-glucopyranosyl)-α-L-arabinoside] (colubrinoside) and jujubogenin-3-O- [2-O-acetyl -3-O- (2-O- β -D- xylopyranosyl-β-D-glucopyranosyl)-α-L-arabinoside] (colubrin) respectively. Both saponins inhibit the spontaneous motility of mice, even at low doses (1 mg/ kg), they show an antagonistic effect on amphetamine and exert a synergistic activity on chlordiazepoxide.

3 From the thesis S. OTT, Munich 1980.

4 Dr. MORTON (Collectanea, Miami, Coral Gables).

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