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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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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. |
format | Online Article Text |
id | pubmed-6259639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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