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Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones

To search for possible anti-tumor agents or anti-tumor promoters among natural or synthetic products, we used cyclic voltammetry to determine the reduction-oxidation potentials of heterocyclic quinones in phosphate buffer at pH 7.2. We determined the growth inhibitory- and cytotoxic activities of 12...

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Detalles Bibliográficos
Autores principales: Koyama, Junko, Morita, Izumi, Yamori, Takao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257668/
https://www.ncbi.nlm.nih.gov/pubmed/20877243
http://dx.doi.org/10.3390/molecules15096559
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author Koyama, Junko
Morita, Izumi
Yamori, Takao
author_facet Koyama, Junko
Morita, Izumi
Yamori, Takao
author_sort Koyama, Junko
collection PubMed
description To search for possible anti-tumor agents or anti-tumor promoters among natural or synthetic products, we used cyclic voltammetry to determine the reduction-oxidation potentials of heterocyclic quinones in phosphate buffer at pH 7.2. We determined the growth inhibitory- and cytotoxic activities of 12 heterocyclic quinone anti-tumor agent candidates against a panel of 39 human cancer cell lines (JFCR39). The average concentrations of the heterocyclic quinones required for 50% growth inhibition (GI(50)) against JFCR39 ranged from 0.045 to 13.2 μM, and the 50% lethal concentration (LC(50)) against JFCR39 ranged from 0.398 to 77.7 μM. The average values of GI(50) or LC(50) of the heterocyclic quinones correlated significantly with their reduction potentials. These results suggested that reduction-oxidation potentials could be a useful method for the discovery of novel antitumor agents.
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spelling pubmed-62576682018-12-06 Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones Koyama, Junko Morita, Izumi Yamori, Takao Molecules Article To search for possible anti-tumor agents or anti-tumor promoters among natural or synthetic products, we used cyclic voltammetry to determine the reduction-oxidation potentials of heterocyclic quinones in phosphate buffer at pH 7.2. We determined the growth inhibitory- and cytotoxic activities of 12 heterocyclic quinone anti-tumor agent candidates against a panel of 39 human cancer cell lines (JFCR39). The average concentrations of the heterocyclic quinones required for 50% growth inhibition (GI(50)) against JFCR39 ranged from 0.045 to 13.2 μM, and the 50% lethal concentration (LC(50)) against JFCR39 ranged from 0.398 to 77.7 μM. The average values of GI(50) or LC(50) of the heterocyclic quinones correlated significantly with their reduction potentials. These results suggested that reduction-oxidation potentials could be a useful method for the discovery of novel antitumor agents. MDPI 2010-09-20 /pmc/articles/PMC6257668/ /pubmed/20877243 http://dx.doi.org/10.3390/molecules15096559 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ 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 Article
Koyama, Junko
Morita, Izumi
Yamori, Takao
Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones
title Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones
title_full Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones
title_fullStr Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones
title_full_unstemmed Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones
title_short Correlation between Cytotoxic Activities and Reduction Potentials of Heterocyclic Quinones
title_sort correlation between cytotoxic activities and reduction potentials of heterocyclic quinones
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257668/
https://www.ncbi.nlm.nih.gov/pubmed/20877243
http://dx.doi.org/10.3390/molecules15096559
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