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Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives

Tuberculosis (TB) is a truly global disease, found in every country on earth. One-third of humanity, over 2 billion people, carry the bacillus that causes TB and 2 million people die of the disease each year. Despite that, no new specific drug against Mycobacterium tuberculosis has been developed si...

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Autores principales: Pavan, Fernando R., de Carvalho, Gustavo Senra G., da Silva, Adilson D., Leite, Clarice Q. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: TheScientificWorldJOURNAL 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720119/
https://www.ncbi.nlm.nih.gov/pubmed/21623457
http://dx.doi.org/10.1100/tsw.2011.110
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author Pavan, Fernando R.
de Carvalho, Gustavo Senra G.
da Silva, Adilson D.
Leite, Clarice Q. F.
author_facet Pavan, Fernando R.
de Carvalho, Gustavo Senra G.
da Silva, Adilson D.
Leite, Clarice Q. F.
author_sort Pavan, Fernando R.
collection PubMed
description Tuberculosis (TB) is a truly global disease, found in every country on earth. One-third of humanity, over 2 billion people, carry the bacillus that causes TB and 2 million people die of the disease each year. Despite that, no new specific drug against Mycobacterium tuberculosis has been developed since the 1960s. There are several candidates for new anti-TB agents, but none proven clinically effective. Stilbenes are compounds found in numerous medicinal plants and food products with some known biological and even antimycobacterial activity. This paper describes the synthesis and the anti–M. tuberculosis activity of eight stilbene analogues. The synthesis and characterization of these compounds are shown, and the results compared with one “first”-line drug used in current therapy.
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spelling pubmed-57201192017-12-21 Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives Pavan, Fernando R. de Carvalho, Gustavo Senra G. da Silva, Adilson D. Leite, Clarice Q. F. ScientificWorldJournal Research Article Tuberculosis (TB) is a truly global disease, found in every country on earth. One-third of humanity, over 2 billion people, carry the bacillus that causes TB and 2 million people die of the disease each year. Despite that, no new specific drug against Mycobacterium tuberculosis has been developed since the 1960s. There are several candidates for new anti-TB agents, but none proven clinically effective. Stilbenes are compounds found in numerous medicinal plants and food products with some known biological and even antimycobacterial activity. This paper describes the synthesis and the anti–M. tuberculosis activity of eight stilbene analogues. The synthesis and characterization of these compounds are shown, and the results compared with one “first”-line drug used in current therapy. TheScientificWorldJOURNAL 2011-05-26 /pmc/articles/PMC5720119/ /pubmed/21623457 http://dx.doi.org/10.1100/tsw.2011.110 Text en Copyright © 2011 Fernando R. Pavan et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Pavan, Fernando R.
de Carvalho, Gustavo Senra G.
da Silva, Adilson D.
Leite, Clarice Q. F.
Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives
title Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives
title_full Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives
title_fullStr Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives
title_full_unstemmed Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives
title_short Synthesis and Anti–Mycobacterium tuberculosis Evaluation of Aza-Stilbene Derivatives
title_sort synthesis and anti–mycobacterium tuberculosis evaluation of aza-stilbene derivatives
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720119/
https://www.ncbi.nlm.nih.gov/pubmed/21623457
http://dx.doi.org/10.1100/tsw.2011.110
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