Biological activity of monoquaternary ammonium compounds based on 3-substituted quinuclidine: A short review

IF 0.2 4区 生物学 Q4 BIOLOGY Periodicum Biologorum Pub Date : 2020-12-30 DOI:10.18054/PB.V121-122I1-2.10603
R. Odžak
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引用次数: 1

Abstract

Quaternary ammonium compounds (QACs) have a long-known application as antiseptics and disinfectants applied in various industries such as pharmaceutical, agricultural and food industry. Given the alarming number of QACs resistant bacteria, there is an urgent need to develop new QACs with broad-spectrum antimicrobial activities and low tendency to trigger bacterial resistance. One recently proposed approach to develop new QACs is based on quaternization of natural products, which proved to be successful. Quinuclidine is an interesting natural precursor find to be a part of the structure of biologically active cinchona alkaloids. In addition to the well-established medicinal and pharmaceutical potential of 3-substituted quinuclidines, QACs based on 3-substituted quinuclidines, have only recently been shown to exhibit a significant antimicrobial activity. Most importantly, these compounds exhibit low toxicity toward normal human cell lines, which opens up a new chapter in the QACs field ensuring further investigation of possible therapeutic application of 3-substituted quinuclidine based QACs.
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3-取代喹啉类单季铵盐化合物的生物活性研究进展
季铵化合物(QACs)作为防腐剂和消毒剂在制药、农业和食品工业等各个行业都有广泛的应用。鉴于QACs耐药菌数量惊人,迫切需要开发具有广谱抗菌活性和低耐药倾向的新型QACs。最近提出的一种开发新型QACs的方法是基于天然产物的季铵化,这种方法被证明是成功的。喹啉是一种有趣的天然前体,是具有生物活性的金鸡纳生物碱结构的一部分。除了3-取代喹啉具有良好的药用和制药潜力外,基于3-取代喹啉的QACs直到最近才被证明具有显著的抗菌活性。最重要的是,这些化合物对正常人类细胞系具有低毒性,这为QACs领域开辟了新的篇章,为进一步研究基于3-取代喹啉的QACs可能的治疗应用提供了基础。
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来源期刊
Periodicum Biologorum
Periodicum Biologorum 生物-生物学
CiteScore
0.80
自引率
0.00%
发文量
16
审稿时长
6-12 weeks
期刊介绍: This journal provides immediate open access to its content on the principle that making research freely available to the public supports a greater global exchange of knowledge.
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