Exploring the correlation of linker structure and antimicrobial activities of pyridinium-based cationic biocides: Aromatic versus aliphatic architectures

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL
Nikita A. Frolov , Mary A. Seferyan , Elena V. Detusheva , Evgeniya A. Saverina , Elizabeth Son , Radmir N. Akchurin , Alena S. Kartseva , Victoria V. Firstova , Anatoly N. Vereshchagin
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引用次数: 0

Abstract

Cationic biocides, particularly quaternary ammonium compounds (QACs), play a vital role in controlling microbial infections across various industries, healthcare facilities and households. As their widespread use increased drastically in the last few years due to COVID-19, there is growing concern about the development of resistance among microorganisms exposed to cationic biocides. It is crucial to recognize this threat in advance and respond by modifying and replacing the old generation of commercial biocides. Reported here is the pyridinium-based bis-QACs tuning via combination of two simple synthesis approaches to achieve novel biocide's architectures with mixed linkers. The obtained compounds were subjected to a broad bioactivity assay against a panel of 26 microbial pathogens, including multi-resistant bacterial ESKAPEE strains, fungi and biofilms. Novel hit-compounds showed improved antibacterial and antibiofilm action, rapid bacterial eradication within 15–30 min of exposure and 4.5-fold lower hemotoxicity, as well as lower potential for the development of bacterial resistance compared to commercial lead antiseptic octenidine. Highlighted findings and insights will serve as a good basis for further studies of bis-QACs as highly effective biocides.

Abstract Image

Abstract Image

探索吡啶基阳离子杀菌剂的连接结构与抗菌活性的相关性:芳香与脂肪族结构
阳离子杀菌剂,特别是季铵化合物(QACs),在控制各种行业、医疗设施和家庭的微生物感染方面发挥着至关重要的作用。由于COVID-19疫情,阳离子杀菌剂的广泛使用在过去几年中急剧增加,人们越来越担心暴露于阳离子杀菌剂的微生物会产生耐药性。至关重要的是要提前认识到这一威胁,并通过修改和更换老一代商业杀菌剂来应对。本文报道了通过结合两种简单的合成方法,以吡啶为基础的双qacs调优,实现了具有混合连接剂的新型杀菌剂结构。获得的化合物对26种微生物病原体进行了广泛的生物活性测定,包括多重耐药细菌ESKAPEE菌株、真菌和生物膜。新型hit-化合物具有更好的抗菌和抗生物膜作用,暴露在15-30分钟内快速根除细菌,血液毒性降低4.5倍,并且与商业铅防腐辛替尼相比,细菌耐药性的发展潜力更低。突出的发现和见解将为进一步研究双- qacs作为高效杀菌剂提供良好的基础。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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