structural antitumoral activity relationships of synthetic chalcones合成化合物的结构antitumoral活动关系.pdf
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Int. J. Mol. Sci. 2009, 10, 221-231; doi:10.3390/ijm
OPEN ACCESS
International Journal of
Molecular Sciences
ISSN 1422-0067
/journal/ijms
Article
Structural Antitumoral Activity Relationships of Synthetic
Chalcones
Cesar Echeverria 1, Juan Francisco Santibañez 1, Oscar Donoso-Tauda 2, Carlos A. Escobar 2 and
Rodrigo Ramirez-Tagle 2,*
1 Instituto de Nutrición y Tecnología de los Alimentos, Universidad de Chile, El Líbano 5524,
Macul, Santiago, Chile. E-Mails: cecheverrriae@ (C. E.); jfsatib@inta.cl (J. S.)
2 Universidad Andres Bello, Departamento de Ciencias Químicas, Av. República 275, Santiago,
Chile. E-Mails: o.donoso@ (O. D.); cescobar@unab.cl (C. E.)
* Author to whom correspondence should be addressed; E-Mail: ralquim@;
Tel. +56-2-6615880
Received: 30 September 2008; in revised form: 31 December 2008 / Accepted: 4 January 2009 /
Published: 9 January 2009
Abstract: Relationships between the structural characteristic of synthetic chalcones and
their antitumoral activity were studied. Treatment of HepG2 cells for 24 h with synthetic
2’-hydroxychalcones resulted in apoptosis induction and dose-dependent inhibition of
cell proliferation. The calculated reactivity indexes and the adiabatic electron affinities
using the DFT method including solvent effects, suggest a structure-activity relationship
between the Chalcones structure and th
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