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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2014
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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. |
format | Online Article Text |
id | pubmed-4033545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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