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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2009
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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. |
format | Text |
id | pubmed-2662465 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
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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