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In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates
The resistance to antimicrobial agents brings a need of novel antimicrobial agents. We have synthesized and found the in vitro antibacterial activity of salicylanilide esters with benzoic acid (2-(phenylcarbamoyl)phenyl benzoates) in micromolar range. They were evaluated in vitro for the activity ag...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Scientific World Journal
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3361159/ https://www.ncbi.nlm.nih.gov/pubmed/22666101 http://dx.doi.org/10.1100/2012/290628 |
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author | Krátký, Martin Vinšová, Jarmila Buchta, Vladimír |
author_facet | Krátký, Martin Vinšová, Jarmila Buchta, Vladimír |
author_sort | Krátký, Martin |
collection | PubMed |
description | The resistance to antimicrobial agents brings a need of novel antimicrobial agents. We have synthesized and found the in vitro antibacterial activity of salicylanilide esters with benzoic acid (2-(phenylcarbamoyl)phenyl benzoates) in micromolar range. They were evaluated in vitro for the activity against eight fungal and eight bacterial species. All derivatives showed a significant antibacterial activity against Gram-positive strains with minimum inhibitory concentrations ≥0.98 μmol/L including methicillin-resistant Staphylococcus aureus strain. The most active compounds were 5-chloro-2-(3,4-dichlorophenylcarbamoyl)phenyl benzoate and 4-chloro-2-(4-(trifluoromethyl)phenylcarbamoyl)phenyl benzoate. The antifungal activity is significantly lower. |
format | Online Article Text |
id | pubmed-3361159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | The Scientific World Journal |
record_format | MEDLINE/PubMed |
spelling | pubmed-33611592012-06-04 In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates Krátký, Martin Vinšová, Jarmila Buchta, Vladimír ScientificWorldJournal Research Article The resistance to antimicrobial agents brings a need of novel antimicrobial agents. We have synthesized and found the in vitro antibacterial activity of salicylanilide esters with benzoic acid (2-(phenylcarbamoyl)phenyl benzoates) in micromolar range. They were evaluated in vitro for the activity against eight fungal and eight bacterial species. All derivatives showed a significant antibacterial activity against Gram-positive strains with minimum inhibitory concentrations ≥0.98 μmol/L including methicillin-resistant Staphylococcus aureus strain. The most active compounds were 5-chloro-2-(3,4-dichlorophenylcarbamoyl)phenyl benzoate and 4-chloro-2-(4-(trifluoromethyl)phenylcarbamoyl)phenyl benzoate. The antifungal activity is significantly lower. The Scientific World Journal 2012-04-30 /pmc/articles/PMC3361159/ /pubmed/22666101 http://dx.doi.org/10.1100/2012/290628 Text en Copyright © 2012 Martin Krátký 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 Krátký, Martin Vinšová, Jarmila Buchta, Vladimír In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates |
title |
In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates |
title_full |
In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates |
title_fullStr |
In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates |
title_full_unstemmed |
In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates |
title_short |
In Vitro Antibacterial and Antifungal Activity of Salicylanilide Benzoates |
title_sort | in vitro antibacterial and antifungal activity of salicylanilide benzoates |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3361159/ https://www.ncbi.nlm.nih.gov/pubmed/22666101 http://dx.doi.org/10.1100/2012/290628 |
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