Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da Universidade Federal do Ceará (UFC) |
Texto Completo: | http://www.repositorio.ufc.br/handle/riufc/10828 |
Resumo: | 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, Gramnegative, 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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Repositório Institucional da Universidade Federal do Ceará (UFC) |
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Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivativesResistência a MedicamentosTiazolidinasAntibiotic 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, Gramnegative, 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.BioMed Research International2015-03-03T13:56:12Z2015-03-03T13:56:12Z2014-05info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfSILVA, I. M. et al. Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives. BioMed Research International, v. 2014, p. 1-9, maio, 2014.http://www.repositorio.ufc.br/handle/riufc/10828Silva, Ivanildo Mangueira daSilva Filho, João daSantiago, Priscila Brandão Gomes da SilvaEgito, Micalyne Soares doSouza, Carlos André deGouveia, Frederico LeiteXimenes, Rafael MatosSena, Kêsia Xisto da Fonseca Ribeiro deFaria, Antonio Rodolfo deBrondani, Dalci JoséAlbuquerque, Julianna Ferreira Cavalcanti deengreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2023-08-08T12:31:21Zoai:repositorio.ufc.br:riufc/10828Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:34:16.516225Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false |
dc.title.none.fl_str_mv |
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 |
spellingShingle |
Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives Silva, Ivanildo Mangueira da Resistência a Medicamentos Tiazolidinas |
title_short |
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_sort |
Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives |
author |
Silva, Ivanildo Mangueira da |
author_facet |
Silva, Ivanildo Mangueira da Silva Filho, João da Santiago, Priscila Brandão Gomes da Silva Egito, Micalyne Soares do Souza, Carlos André de Gouveia, Frederico Leite Ximenes, Rafael Matos Sena, Kêsia Xisto da Fonseca Ribeiro de Faria, Antonio Rodolfo de Brondani, Dalci José Albuquerque, Julianna Ferreira Cavalcanti de |
author_role |
author |
author2 |
Silva Filho, João da Santiago, Priscila Brandão Gomes da Silva Egito, Micalyne Soares do Souza, Carlos André de Gouveia, Frederico Leite Ximenes, Rafael Matos Sena, Kêsia Xisto da Fonseca Ribeiro de Faria, Antonio Rodolfo de Brondani, Dalci José Albuquerque, Julianna Ferreira Cavalcanti de |
author2_role |
author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Silva, Ivanildo Mangueira da Silva Filho, João da Santiago, Priscila Brandão Gomes da Silva Egito, Micalyne Soares do Souza, Carlos André de Gouveia, Frederico Leite Ximenes, Rafael Matos Sena, Kêsia Xisto da Fonseca Ribeiro de Faria, Antonio Rodolfo de Brondani, Dalci José Albuquerque, Julianna Ferreira Cavalcanti de |
dc.subject.por.fl_str_mv |
Resistência a Medicamentos Tiazolidinas |
topic |
Resistência a Medicamentos Tiazolidinas |
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, Gramnegative, 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. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-05 2015-03-03T13:56:12Z 2015-03-03T13:56:12Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
SILVA, I. M. et al. Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives. BioMed Research International, v. 2014, p. 1-9, maio, 2014. http://www.repositorio.ufc.br/handle/riufc/10828 |
identifier_str_mv |
SILVA, I. M. et al. Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives. BioMed Research International, v. 2014, p. 1-9, maio, 2014. |
url |
http://www.repositorio.ufc.br/handle/riufc/10828 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
BioMed Research International |
publisher.none.fl_str_mv |
BioMed Research International |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da Universidade Federal do Ceará (UFC) instname:Universidade Federal do Ceará (UFC) instacron:UFC |
instname_str |
Universidade Federal do Ceará (UFC) |
instacron_str |
UFC |
institution |
UFC |
reponame_str |
Repositório Institucional da Universidade Federal do Ceará (UFC) |
collection |
Repositório Institucional da Universidade Federal do Ceará (UFC) |
repository.name.fl_str_mv |
Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC) |
repository.mail.fl_str_mv |
bu@ufc.br || repositorio@ufc.br |
_version_ |
1813028859611709440 |