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In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine

2,9-Dimethoxymethylboldine (2), 2,9-dimethoxymethyl-3-bromoboldine (3) and 2,9-dimethoxymethyl-3-diphenylphosphinylboldine (4) have been synthesized in an effort to find compounds with potential pharmacological applications. The cytotoxic activities of the natural precursor 1 and these three derivat...

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Detalles Bibliográficos
Autores principales: Thomet, Franz A., Piñol, Pablo, Villena, Joan, Reveco, Patricio G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259639/
https://www.ncbi.nlm.nih.gov/pubmed/21383661
http://dx.doi.org/10.3390/molecules16032253
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author Thomet, Franz A.
Piñol, Pablo
Villena, Joan
Reveco, Patricio G.
author_facet Thomet, Franz A.
Piñol, Pablo
Villena, Joan
Reveco, Patricio G.
author_sort Thomet, Franz A.
collection PubMed
description 2,9-Dimethoxymethylboldine (2), 2,9-dimethoxymethyl-3-bromoboldine (3) and 2,9-dimethoxymethyl-3-diphenylphosphinylboldine (4) have been synthesized in an effort to find compounds with potential pharmacological applications. The cytotoxic activities of the natural precursor 1 and these three derivatives have been measured as IC(50) inhibitory growth. The diphenylphosphinyl derivative 4 showed a significant cytotoxic activity on two breast cancer cell lines, namely MCF-7 and MDA-MB-231, with IC(50) values of 55.5 and 62.7 [µM], respectively. These results suggest that the kind of structural modifications introduced to synthesize compound 4 represent a promising way to enhance the cytotoxic activity of boldine derivatives.
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spelling pubmed-62596392018-12-07 In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine Thomet, Franz A. Piñol, Pablo Villena, Joan Reveco, Patricio G. Molecules Communication 2,9-Dimethoxymethylboldine (2), 2,9-dimethoxymethyl-3-bromoboldine (3) and 2,9-dimethoxymethyl-3-diphenylphosphinylboldine (4) have been synthesized in an effort to find compounds with potential pharmacological applications. The cytotoxic activities of the natural precursor 1 and these three derivatives have been measured as IC(50) inhibitory growth. The diphenylphosphinyl derivative 4 showed a significant cytotoxic activity on two breast cancer cell lines, namely MCF-7 and MDA-MB-231, with IC(50) values of 55.5 and 62.7 [µM], respectively. These results suggest that the kind of structural modifications introduced to synthesize compound 4 represent a promising way to enhance the cytotoxic activity of boldine derivatives. MDPI 2011-03-07 /pmc/articles/PMC6259639/ /pubmed/21383661 http://dx.doi.org/10.3390/molecules16032253 Text en © 2011 by the authors; licensee MDPI, 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/).
spellingShingle Communication
Thomet, Franz A.
Piñol, Pablo
Villena, Joan
Reveco, Patricio G.
In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine
title In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine
title_full In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine
title_fullStr In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine
title_full_unstemmed In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine
title_short In Vitro Cytotoxic Evaluation of a Novel Phosphinyl Derivative of Boldine
title_sort in vitro cytotoxic evaluation of a novel phosphinyl derivative of boldine
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259639/
https://www.ncbi.nlm.nih.gov/pubmed/21383661
http://dx.doi.org/10.3390/molecules16032253
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