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BY-NC-ND 3.0 license Open Access Published by De Gruyter June 2, 2014

Trypanocidal Activity of Abietane Diterpenoids from the Roots of Craniolaria annua

  • Julio C. Herrera EMAIL logo , Graciela Troncone , Diana Henríquez and Neudo Urdaneta

Abstract

A chloroform extract from roots of Craniolaria annua provided six new C-11 unsubstituted abietanes, 14-hydroxy-6,12-dione-7,9(11),13-abietatriene (1), 14-hydroxy-12-oxo-7,9(11),13- abietatriene (2), 6,12,14-trihydroxyabieta-5,8,11,13-tetraen-7-one (3), ar-abietatriene-12-ol- 6,7-dione-14,16-oxide (4), ar-abietatriene-12,16-diol-14,16-oxide (5) and ar-abietatriene-12-ol- 7-one-14,16-oxide (6), and two known compounds, ferruginol and stigmasterol. The structures of both the new and known compounds were established by spectroscopic methods. Abietane 1 gave 14-hydroxy-6-oxoferruginol (1A) upon treatment with NaBH4. Abietanes 1, 1A, 3-5 and ferruginol showed cytotoxic effects against trypomastigote and epimastigote forms of Trypanosoma cruzi and against fibroblastic Vero cells.

Received: 2008-4-9
Revised: 2008-6-23
Published Online: 2014-6-2
Published in Print: 2008-12-1

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