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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...

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Detalles Bibliográficos
Autores principales: Krátký, Martin, Vinšová, Jarmila, Buchta, Vladimír
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific World Journal 2012
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.
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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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