Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity

Detalhes bibliográficos
Autor(a) principal: Çoban, Esin Poyrazoğlu
Data de Publicação: 2017
Outros Autores: Fırıncı, Rukiye, Biyik, Halil, Günay, Muhammet Emin
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/131415
Resumo: Unsymmetrically substituted imidazolium salts were synthesized and characterized using 1H-NMR and 13C-NMR. The antimicrobial activities of the salts were evaluated using the agar-well diffusion method against 14 bacteria and five yeasts. The minimal inhibitory concentrations (MIC) against seven bacteria and one yeast were also determined. Among the test compounds applied, 1, 2, 3, 6 and 11 showed activities against Micrococcus luteus ATCC 9341, Staphylococcus aureus ATCC 25923, Staphylococcus epidermidis ATCC 12228, Bacilllus cereus ATCC 11778, Bacillus subtilis ATCC 6633, Bacillus thuringiensis, Listeria monocytogenes ATCC 19112 and Candida trophicalis. However, compounds 1, 2 and 3 showed the highest antimicrobial activities against Micrococcus luteus ATCC 9341, Stapylococcus aureus ATCC 25923, Staphylococcus epidermidis ATCC 12228, Bacilllus cereus ATCC 11778 and Bacillus subtilis ATCC 6633 with inhibition zones of 14-20 mm. In addition, compound 6 have only demonstrated activities against Candida trophicalis while compounds 4, 5, 7, 8, 9, 10, 12, 13 and 14 had no effect on test microorganisms.
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spelling Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activityImidazolium salts/characterizationN-heterocyclic carbenesImidazolium salts/antimicrobial activityImidazolium salts/Minimum inhibitory concentration.Unsymmetrically substituted imidazolium salts were synthesized and characterized using 1H-NMR and 13C-NMR. The antimicrobial activities of the salts were evaluated using the agar-well diffusion method against 14 bacteria and five yeasts. The minimal inhibitory concentrations (MIC) against seven bacteria and one yeast were also determined. Among the test compounds applied, 1, 2, 3, 6 and 11 showed activities against Micrococcus luteus ATCC 9341, Staphylococcus aureus ATCC 25923, Staphylococcus epidermidis ATCC 12228, Bacilllus cereus ATCC 11778, Bacillus subtilis ATCC 6633, Bacillus thuringiensis, Listeria monocytogenes ATCC 19112 and Candida trophicalis. However, compounds 1, 2 and 3 showed the highest antimicrobial activities against Micrococcus luteus ATCC 9341, Stapylococcus aureus ATCC 25923, Staphylococcus epidermidis ATCC 12228, Bacilllus cereus ATCC 11778 and Bacillus subtilis ATCC 6633 with inhibition zones of 14-20 mm. In addition, compound 6 have only demonstrated activities against Candida trophicalis while compounds 4, 5, 7, 8, 9, 10, 12, 13 and 14 had no effect on test microorganisms.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2017-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/13141510.1590/s2175-97902017000115075Brazilian Journal of Pharmaceutical Sciences; Vol. 53 Núm. 1 (2017); e15075-Brazilian Journal of Pharmaceutical Sciences; v. 53 n. 1 (2017); e15075-Brazilian Journal of Pharmaceutical Sciences; Vol. 53 No. 1 (2017); e15075-2175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/131415/127795Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)info:eu-repo/semantics/openAccessÇoban, Esin PoyrazoğluFırıncı, RukiyeBiyik, HalilGünay, Muhammet Emin2017-04-20T20:28:50Zoai:revistas.usp.br:article/131415Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2017-04-20T20:28:50Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
title Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
spellingShingle Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
Çoban, Esin Poyrazoğlu
Imidazolium salts/characterization
N-heterocyclic carbenes
Imidazolium salts/antimicrobial activity
Imidazolium salts/Minimum inhibitory concentration.
title_short Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
title_full Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
title_fullStr Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
title_full_unstemmed Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
title_sort Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
author Çoban, Esin Poyrazoğlu
author_facet Çoban, Esin Poyrazoğlu
Fırıncı, Rukiye
Biyik, Halil
Günay, Muhammet Emin
author_role author
author2 Fırıncı, Rukiye
Biyik, Halil
Günay, Muhammet Emin
author2_role author
author
author
dc.contributor.author.fl_str_mv Çoban, Esin Poyrazoğlu
Fırıncı, Rukiye
Biyik, Halil
Günay, Muhammet Emin
dc.subject.por.fl_str_mv Imidazolium salts/characterization
N-heterocyclic carbenes
Imidazolium salts/antimicrobial activity
Imidazolium salts/Minimum inhibitory concentration.
topic Imidazolium salts/characterization
N-heterocyclic carbenes
Imidazolium salts/antimicrobial activity
Imidazolium salts/Minimum inhibitory concentration.
description Unsymmetrically substituted imidazolium salts were synthesized and characterized using 1H-NMR and 13C-NMR. The antimicrobial activities of the salts were evaluated using the agar-well diffusion method against 14 bacteria and five yeasts. The minimal inhibitory concentrations (MIC) against seven bacteria and one yeast were also determined. Among the test compounds applied, 1, 2, 3, 6 and 11 showed activities against Micrococcus luteus ATCC 9341, Staphylococcus aureus ATCC 25923, Staphylococcus epidermidis ATCC 12228, Bacilllus cereus ATCC 11778, Bacillus subtilis ATCC 6633, Bacillus thuringiensis, Listeria monocytogenes ATCC 19112 and Candida trophicalis. However, compounds 1, 2 and 3 showed the highest antimicrobial activities against Micrococcus luteus ATCC 9341, Stapylococcus aureus ATCC 25923, Staphylococcus epidermidis ATCC 12228, Bacilllus cereus ATCC 11778 and Bacillus subtilis ATCC 6633 with inhibition zones of 14-20 mm. In addition, compound 6 have only demonstrated activities against Candida trophicalis while compounds 4, 5, 7, 8, 9, 10, 12, 13 and 14 had no effect on test microorganisms.
publishDate 2017
dc.date.none.fl_str_mv 2017-01-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjps/article/view/131415
10.1590/s2175-97902017000115075
url https://www.revistas.usp.br/bjps/article/view/131415
identifier_str_mv 10.1590/s2175-97902017000115075
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/131415/127795
dc.rights.driver.fl_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2018 Brazilian Journal of Pharmaceutical Sciences (Impresso)
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 53 Núm. 1 (2017); e15075-
Brazilian Journal of Pharmaceutical Sciences; v. 53 n. 1 (2017); e15075-
Brazilian Journal of Pharmaceutical Sciences; Vol. 53 No. 1 (2017); e15075-
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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