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新型双子季铵盐的合成及广谱杀菌效果。

Synthesis and broad-spectrum biocidal effect of novel gemini quaternary ammonium compounds.

机构信息

Department of Toxicology and Military Pharmacy, Military Faculty of Medicine, University of Defence, Trebesska 1575, 500 05 Hradec Kralove, Czech Republic; Biomedical Research Centre, University Hospital Hradec Kralove, Sokolska 581, 500 05 Hradec Kralove, Czech Republic.

Biomedical Research Centre, University Hospital Hradec Kralove, Sokolska 581, 500 05 Hradec Kralove, Czech Republic.

出版信息

Bioorg Chem. 2024 Oct;151:107646. doi: 10.1016/j.bioorg.2024.107646. Epub 2024 Jul 15.

Abstract

Since the discovery of antimicrobial agents, the misuse of antibiotics has led to the emergence of bacterial strains resistant to both antibiotics and common disinfectants like quaternary ammonium compounds (QACs). A new class, 'gemini' QACs, which contain two polar heads, has shown promise. Octenidine (OCT), a representative of this group, is effective against resistant microorganisms but has limitations such as low solubility and high cytotoxicity. In this study, we developed 16 novel OCT derivatives. These compounds were subjected to in silico screening to predict their membrane permeation. Testing against nosocomial bacterial strains (G and G) and their biofilms revealed that most compounds were highly effective against G bacteria, while compounds 7, 8, and 10-12 were effective against G bacteria. Notably, compounds 6-8 were significantly more effective than OCT and BAC standards across the bacterial panel. Compound 12 stood out due to its low cytotoxicity and broad-spectrum antimicrobial activity, comparable to OCT. It also demonstrated impressive antifungal activity. Compound 1 was highly selective to fungi and four times more effective than OCT without its cytotoxicity. Several compounds, including 4, 6, 8, 9, 10, and 12, showed strong virucidal activity against murine cytomegalovirus and herpes simplex virus 1. In conclusion, these gemini QACs, especially compound 12, offer a promising alternative to current disinfectants, addressing emerging resistances with their enhanced antimicrobial, antifungal, and virucidal properties.

摘要

自抗菌剂问世以来,抗生素的滥用导致了细菌菌株对抗生素和常见消毒剂(如季铵化合物(QACs))的耐药性的出现。一类新的“双子”QACs 含有两个极性头,显示出了前景。作为该组的代表物,奥替尼啶(OCT)对耐药微生物有效,但存在溶解度低和细胞毒性高的局限性。在这项研究中,我们开发了 16 种新型 OCT 衍生物。这些化合物经过计算机筛选以预测其膜通透性。对医院细菌菌株(G 和 G)及其生物膜的测试表明,大多数化合物对 G 细菌高度有效,而化合物 7、8 和 10-12 对 G 细菌有效。值得注意的是,化合物 6-8 在整个细菌组中比 OCT 和 BAC 标准物更有效。由于其低细胞毒性和广谱抗菌活性,与 OCT 相当,化合物 12 脱颖而出。它还表现出令人印象深刻的抗真菌活性。化合物 1 对真菌具有高度选择性,其效力是 OCT 的四倍,且没有细胞毒性。包括 4、6、8、9、10 和 12 在内的几种化合物对鼠巨细胞病毒和单纯疱疹病毒 1 具有很强的杀病毒活性。总之,这些双子 QACs,特别是化合物 12,为当前消毒剂提供了一种有前途的替代品,其增强的抗菌、抗真菌和杀病毒特性解决了新兴的耐药性问题。

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