Leishmanicidal cycloartane-type triterpene glycosides from Astragalus oleifolius

Ozipek M., Donmez A., Calis I. , Brun R., Ruedi P., Tasdemir D.

PHYTOCHEMISTRY, vol.66, no.10, pp.1168-1173, 2005 (Journal Indexed in SCI) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 66 Issue: 10
  • Publication Date: 2005
  • Doi Number: 10.1016/j.phytochem.2005.04.019
  • Title of Journal : PHYTOCHEMISTRY
  • Page Numbers: pp.1168-1173


Two new cycloartane-type glycosides oleifoliosides A (1) and B (2) were isolated from the lower stem parts of Astragalus oleifolius. Their structures were identified as 3-O-[beta-xylopyranosyl-(1 -> 2)-alpha-arabinopyranosyl]-6-O-p-xylopyranosyl-3 beta,6 alpha,16 beta, 24(S),25-pentahydroxycycloartane and 3-O-[beta-xylopyranosyl-(1 -> 2)-alpha-arabinopyranosyll-6-O-beta-glueopyranosyl-3 beta,6 alpha,16 beta,24(S), 25-pentahydroxycycloartane, respectively, by means of spectroscopic methods (IR, ID and 2D NMR, ESI-MS). Three known cycloartane glycosides cyclocanthoside E (3), astragaloside 11 (4) and astragaloside IV (5) were also isolated and characterized. All five compounds were evaluated for in vitro trypanocidal, leishmanicidal and antiplasmodial activities as well as their cytotoxic potential on primary mammalian (L6) cells. Except for the compound 5, all compounds showed notable growth inhibitory activity against Leishmania donovani with IC50 Values ranging from 13.2 to 21.3 mu g/ml. Only weak activity against Trypanosoma brucci rhodesiense was observed with the known compounds astragaloside 11 (4, IC50 66.6 mu g/ml) and cyclocanthoside E (3, IC50 85.2 mu g/ml), while all compounds were inactive against Trypanosoma cruzi and Plasmodium falciparum. None of the compounds were toxic to mammalian cells (IC50'S > 90 mu g/ml). This is the first report of leishmanicidal and trypanocidal activity of cycloartane-type triterpene glycosides. (c) 2005 Elsevier Ltd. All rights reserved.