Synthesis and antimicrobial activities of 5-arylidene-thiazolidine-2,4-dione derivatives

Detalhes bibliográficos
Autor(a) principal: Silva, Ivanildo Mangueira da
Data de Publicação: 2014
Outros Autores: 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
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.
id UFC-7_d3403aa8abb9786c3f75ebcd72f94769
oai_identifier_str oai:repositorio.ufc.br:riufc/10828
network_acronym_str UFC-7
network_name_str Repositório Institucional da Universidade Federal do Ceará (UFC)
repository_id_str
spelling 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