1. Academic Validation
  2. Cytotoxic pentacyclic triterpenoids from Combretum sundaicum and Lantana camara as inhibitors of Bcl-xL/BakBH3 domain peptide interaction

Cytotoxic pentacyclic triterpenoids from Combretum sundaicum and Lantana camara as inhibitors of Bcl-xL/BakBH3 domain peptide interaction

  • J Nat Prod. 2009 Jul;72(7):1314-20. doi: 10.1021/np900192r.
Marc Litaudon 1 Claire Jolly Catherine Le Callonec Dao Din Cuong Pascal Retailleau Olivier Nosjean Van Hung Nguyen Bruno Pfeiffer Jean A Boutin Françoise Guéritte
Affiliations

Affiliation

  • 1 Institut de Chimie des Substances Naturelles, UPR2301, CNRS, 91198 Gif-sur-Yvette, France. [email protected]
Abstract

In an effort to discover potent inhibitors of the antiapoptotic protein Bcl-xL, a systematic in vitro evaluation was undertaken on extracts prepared from various parts of Vietnamese Plants. The ethyl acetate extracts obtained from the leaves and flowers of Combretum sundaicum and the leaves of Lantana camara were selected for their interaction with the Bcl-xL/Bak association. Bioassay-guided purification of these species led to the isolation of 15 Pentacyclic Triterpenoids (1-15) possessing olean-12-en-28-oic acid and olean-12-en-29-oic acid aglycons, of which compounds 1-6 and 8-10 are new. Five compounds exhibited binding activity with K(i) values between 5.3 and 17.8 microM. The cytotoxic activity of 1-15 was also evaluated on various Cancer cell lines.

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