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Structural Antitumoral Activity Relationships of Synthetic Chalcones

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...

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Autores principales: Echeverria, Cesar, Santibañez, Juan Francisco, Donoso-Tauda, Oscar, Escobar, Carlos A., Ramirez-Tagle, Rodrigo
Formato: Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2662465/
https://www.ncbi.nlm.nih.gov/pubmed/19333443
http://dx.doi.org/10.3390/ijms10010221
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author Echeverria, Cesar
Santibañez, Juan Francisco
Donoso-Tauda, Oscar
Escobar, Carlos A.
Ramirez-Tagle, Rodrigo
author_facet Echeverria, Cesar
Santibañez, Juan Francisco
Donoso-Tauda, Oscar
Escobar, Carlos A.
Ramirez-Tagle, Rodrigo
author_sort Echeverria, Cesar
collection PubMed
description 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 the apoptosis in HepG2 cells. The absence of methoxy substituents in the B ring of synthetic 2’-hydroxychalcones, showed the mayor structure-activity pattern along the series.
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spelling pubmed-26624652009-03-30 Structural Antitumoral Activity Relationships of Synthetic Chalcones Echeverria, Cesar Santibañez, Juan Francisco Donoso-Tauda, Oscar Escobar, Carlos A. Ramirez-Tagle, Rodrigo Int J Mol Sci Article 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 the apoptosis in HepG2 cells. The absence of methoxy substituents in the B ring of synthetic 2’-hydroxychalcones, showed the mayor structure-activity pattern along the series. Molecular Diversity Preservation International (MDPI) 2009-01-09 /pmc/articles/PMC2662465/ /pubmed/19333443 http://dx.doi.org/10.3390/ijms10010221 Text en © 2009 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Echeverria, Cesar
Santibañez, Juan Francisco
Donoso-Tauda, Oscar
Escobar, Carlos A.
Ramirez-Tagle, Rodrigo
Structural Antitumoral Activity Relationships of Synthetic Chalcones
title Structural Antitumoral Activity Relationships of Synthetic Chalcones
title_full Structural Antitumoral Activity Relationships of Synthetic Chalcones
title_fullStr Structural Antitumoral Activity Relationships of Synthetic Chalcones
title_full_unstemmed Structural Antitumoral Activity Relationships of Synthetic Chalcones
title_short Structural Antitumoral Activity Relationships of Synthetic Chalcones
title_sort structural antitumoral activity relationships of synthetic chalcones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2662465/
https://www.ncbi.nlm.nih.gov/pubmed/19333443
http://dx.doi.org/10.3390/ijms10010221
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