Unsymmetrically substituted imidazolium salts: synthesis, characterization and antimicrobial activity
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , |
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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Brazilian Journal of Pharmaceutical Sciences |
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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 |
_version_ |
1800222912899186688 |