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Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker

Eighteen novel gemini quaternary ammonium compounds were synthesized to examine the effect of linker nature, aliphatic chain length and their relative position on antibacterial and antifungal activity. The synthesized compounds showed strong bacteriostatic activity against a panel of both Gram-posit...

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Autores principales: Vereshchagin, Anatoly N., Frolov, Nikita A., Konyuhova, Valeria Yu, Kapelistaya, Ekaterina A., Hansford, Karl A., Egorov, Mikhail P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693992/
https://www.ncbi.nlm.nih.gov/pubmed/35424282
http://dx.doi.org/10.1039/d0ra08900a
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author Vereshchagin, Anatoly N.
Frolov, Nikita A.
Konyuhova, Valeria Yu
Kapelistaya, Ekaterina A.
Hansford, Karl A.
Egorov, Mikhail P.
author_facet Vereshchagin, Anatoly N.
Frolov, Nikita A.
Konyuhova, Valeria Yu
Kapelistaya, Ekaterina A.
Hansford, Karl A.
Egorov, Mikhail P.
author_sort Vereshchagin, Anatoly N.
collection PubMed
description Eighteen novel gemini quaternary ammonium compounds were synthesized to examine the effect of linker nature, aliphatic chain length and their relative position on antibacterial and antifungal activity. The synthesized compounds showed strong bacteriostatic activity against a panel of both Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and two fungi. Some of these compounds exhibited a wider and more potent antimicrobial spectrum than commonly-used antiseptics, such as benzalkonium chloride (BAC), cetylpyridinium chloride (CPC), chlorhexidine digluconate (CHG) and octenidine dihydrochloride (OCT).
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spelling pubmed-86939922022-04-13 Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker Vereshchagin, Anatoly N. Frolov, Nikita A. Konyuhova, Valeria Yu Kapelistaya, Ekaterina A. Hansford, Karl A. Egorov, Mikhail P. RSC Adv Chemistry Eighteen novel gemini quaternary ammonium compounds were synthesized to examine the effect of linker nature, aliphatic chain length and their relative position on antibacterial and antifungal activity. The synthesized compounds showed strong bacteriostatic activity against a panel of both Gram-positive and Gram-negative bacteria, including methicillin-resistant Staphylococcus aureus (MRSA) and two fungi. Some of these compounds exhibited a wider and more potent antimicrobial spectrum than commonly-used antiseptics, such as benzalkonium chloride (BAC), cetylpyridinium chloride (CPC), chlorhexidine digluconate (CHG) and octenidine dihydrochloride (OCT). The Royal Society of Chemistry 2021-01-18 /pmc/articles/PMC8693992/ /pubmed/35424282 http://dx.doi.org/10.1039/d0ra08900a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Vereshchagin, Anatoly N.
Frolov, Nikita A.
Konyuhova, Valeria Yu
Kapelistaya, Ekaterina A.
Hansford, Karl A.
Egorov, Mikhail P.
Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker
title Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker
title_full Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker
title_fullStr Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker
title_full_unstemmed Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker
title_short Investigations into the structure–activity relationship in gemini QACs based on biphenyl and oxydiphenyl linker
title_sort investigations into the structure–activity relationship in gemini qacs based on biphenyl and oxydiphenyl linker
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693992/
https://www.ncbi.nlm.nih.gov/pubmed/35424282
http://dx.doi.org/10.1039/d0ra08900a
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