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Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives

Antibiotic resistance is considered one of the world's major public health concerns. The main cause of bacterial resistance is the improper and repeated use of antibiotics. To alleviate this problem, new chemical substances against microorganisms are being synthesized and tested. Thiazolidines...

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Autores principales: da Silva, Ivanildo Mangueira, da Silva Filho, João, Santiago, Priscila Brandão Gomes da Silva, do Egito, Micalyne Soares, de Souza, Carlos André, Gouveia, Frederico Leite, Ximenes, Rafael Matos, de Sena, Kêsia Xisto da Fonseca Ribeiro, de Faria, Antonio Rodolfo, Brondani, Dalci José, de Albuquerque, Julianna Ferreira Cavalcanti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033545/
https://www.ncbi.nlm.nih.gov/pubmed/24895565
http://dx.doi.org/10.1155/2014/316082
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author da Silva, Ivanildo Mangueira
da Silva Filho, João
Santiago, Priscila Brandão Gomes da Silva
do Egito, Micalyne Soares
de Souza, Carlos André
Gouveia, Frederico Leite
Ximenes, Rafael Matos
de Sena, Kêsia Xisto da Fonseca Ribeiro
de Faria, Antonio Rodolfo
Brondani, Dalci José
de Albuquerque, Julianna Ferreira Cavalcanti
author_facet da Silva, Ivanildo Mangueira
da Silva Filho, João
Santiago, Priscila Brandão Gomes da Silva
do Egito, Micalyne Soares
de Souza, Carlos André
Gouveia, Frederico Leite
Ximenes, Rafael Matos
de Sena, Kêsia Xisto da Fonseca Ribeiro
de Faria, Antonio Rodolfo
Brondani, Dalci José
de Albuquerque, Julianna Ferreira Cavalcanti
author_sort da Silva, Ivanildo Mangueira
collection PubMed
description Antibiotic resistance is considered one of the world's major public health concerns. The main cause of bacterial resistance is the improper and repeated use of antibiotics. To alleviate this problem, new chemical substances against microorganisms are being synthesized and tested. Thiazolidines are compounds having many pharmacological activities including antimicrobial activities. For this purpose some thiazolidine derivatives substituted at position 5 in the thiazolidine nucleus were synthesized and tested against several microorganisms. Using a disc diffusion method, antimicrobial activity was verified against Gram-positive, Gram-negative, and alcohol acid resistant bacteria and yeast. The minimum inhibition concentrations (MIC) and minimum bactericidal concentrations (MBC) were determined. All derivatives showed antimicrobial activity mainly against Gram-positive bacteria, with MIC values ranging from 2 to 16 µg/mL.
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spelling pubmed-40335452014-06-03 Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives da Silva, Ivanildo Mangueira da Silva Filho, João Santiago, Priscila Brandão Gomes da Silva do Egito, Micalyne Soares de Souza, Carlos André Gouveia, Frederico Leite Ximenes, Rafael Matos de Sena, Kêsia Xisto da Fonseca Ribeiro de Faria, Antonio Rodolfo Brondani, Dalci José de Albuquerque, Julianna Ferreira Cavalcanti Biomed Res Int Research Article Antibiotic resistance is considered one of the world's major public health concerns. The main cause of bacterial resistance is the improper and repeated use of antibiotics. To alleviate this problem, new chemical substances against microorganisms are being synthesized and tested. Thiazolidines are compounds having many pharmacological activities including antimicrobial activities. For this purpose some thiazolidine derivatives substituted at position 5 in the thiazolidine nucleus were synthesized and tested against several microorganisms. Using a disc diffusion method, antimicrobial activity was verified against Gram-positive, Gram-negative, and alcohol acid resistant bacteria and yeast. The minimum inhibition concentrations (MIC) and minimum bactericidal concentrations (MBC) were determined. All derivatives showed antimicrobial activity mainly against Gram-positive bacteria, with MIC values ranging from 2 to 16 µg/mL. Hindawi Publishing Corporation 2014 2014-05-07 /pmc/articles/PMC4033545/ /pubmed/24895565 http://dx.doi.org/10.1155/2014/316082 Text en Copyright © 2014 Ivanildo Mangueira da Silva 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
da Silva, Ivanildo Mangueira
da Silva Filho, João
Santiago, Priscila Brandão Gomes da Silva
do Egito, Micalyne Soares
de Souza, Carlos André
Gouveia, Frederico Leite
Ximenes, Rafael Matos
de Sena, Kêsia Xisto da Fonseca Ribeiro
de Faria, Antonio Rodolfo
Brondani, Dalci José
de Albuquerque, Julianna Ferreira Cavalcanti
Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives
title Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives
title_full Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives
title_fullStr Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives
title_full_unstemmed Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives
title_short Synthesis and Antimicrobial Activities of 5-Arylidene-thiazolidine-2,4-dione Derivatives
title_sort synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4033545/
https://www.ncbi.nlm.nih.gov/pubmed/24895565
http://dx.doi.org/10.1155/2014/316082
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