Fiche publication


Date publication

janvier 2011

Auteurs

Membres identifiés du Cancéropôle Est :
Dr DESAUBRY Laurent , Dr GAIDDON Christian


Tous les auteurs :
Thuaud F, Ribeiro N, Gaiddon C, Cresteil T, Desaubry L

Résumé

Novel flavagline analogues were synthesized and examined with respect to their cytotoxicity. Structural features critical to the potential of this class of anticancer natural products were unraveled. We demonstrated, in particular, that the introduction of substituants at C-2 has a deleterious effect on multidrug resistance. Replacement of the hydroxy at C-1 by an aminoformyl with the opposite configuration enhances the cytotoxicity and led to a compound that reduces tumors growth in an allograft model at nontoxic doses.

Référence

J Med Chem. 2011 Jan 13;54(1):411-5