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Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines

Antibiotic resistance is now a global problem, and the lack of effective antimicrobial agents for the treatment of diseases caused by resistant microbes is increasing. The 3-acetyl-2,5-disubstituted-1,3,4-oxadiazolines presented in this article may provide a good starting point for the development o...

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Detalles Bibliográficos
Autores principales: Paruch, Kinga, Biernasiuk, Anna, Berecka-Rycerz, Anna, Hordyjewska, Anna, Popiołek, Łukasz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704594/
https://www.ncbi.nlm.nih.gov/pubmed/34948461
http://dx.doi.org/10.3390/ijms222413669
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author Paruch, Kinga
Biernasiuk, Anna
Berecka-Rycerz, Anna
Hordyjewska, Anna
Popiołek, Łukasz
author_facet Paruch, Kinga
Biernasiuk, Anna
Berecka-Rycerz, Anna
Hordyjewska, Anna
Popiołek, Łukasz
author_sort Paruch, Kinga
collection PubMed
description Antibiotic resistance is now a global problem, and the lack of effective antimicrobial agents for the treatment of diseases caused by resistant microbes is increasing. The 3-acetyl-2,5-disubstituted-1,3,4-oxadiazolines presented in this article may provide a good starting point for the development of potential new effective antimicrobial agents useful in the treatment of bacterial and fungal infections. Particular attention is drawn to the 1,3,4-oxadiazole derivative marked with the number 29 with 5-nitrofuran-2-yl substituent in its chemical structure. This substance showed a strong bactericidal effect, especially against Staphylococcus spp., and no cytotoxicity to the L929 normal cell line.
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spelling pubmed-87045942021-12-25 Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines Paruch, Kinga Biernasiuk, Anna Berecka-Rycerz, Anna Hordyjewska, Anna Popiołek, Łukasz Int J Mol Sci Article Antibiotic resistance is now a global problem, and the lack of effective antimicrobial agents for the treatment of diseases caused by resistant microbes is increasing. The 3-acetyl-2,5-disubstituted-1,3,4-oxadiazolines presented in this article may provide a good starting point for the development of potential new effective antimicrobial agents useful in the treatment of bacterial and fungal infections. Particular attention is drawn to the 1,3,4-oxadiazole derivative marked with the number 29 with 5-nitrofuran-2-yl substituent in its chemical structure. This substance showed a strong bactericidal effect, especially against Staphylococcus spp., and no cytotoxicity to the L929 normal cell line. MDPI 2021-12-20 /pmc/articles/PMC8704594/ /pubmed/34948461 http://dx.doi.org/10.3390/ijms222413669 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Paruch, Kinga
Biernasiuk, Anna
Berecka-Rycerz, Anna
Hordyjewska, Anna
Popiołek, Łukasz
Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines
title Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines
title_full Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines
title_fullStr Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines
title_full_unstemmed Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines
title_short Biological Activity, Lipophilicity and Cytotoxicity of Novel 3-Acetyl-2,5-disubstituted-1,3,4-oxadiazolines
title_sort biological activity, lipophilicity and cytotoxicity of novel 3-acetyl-2,5-disubstituted-1,3,4-oxadiazolines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8704594/
https://www.ncbi.nlm.nih.gov/pubmed/34948461
http://dx.doi.org/10.3390/ijms222413669
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