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新型强效奎宁啶类抗菌药物。

New and Potent Quinuclidine-Based Antimicrobial Agents.

机构信息

Department of Chemistry, Faculty of Science, University of Zagreb, Horvatovac 102a, HR-10000 Zagreb, Croatia.

Department of Chemistry, Faculty of Science, University of Split, R. Boškovića 33, HR-21000 Split, Croatia.

出版信息

Molecules. 2019 Jul 23;24(14):2675. doi: 10.3390/molecules24142675.

Abstract

Developing new antibiotics is currently very important since antibiotic resistance is one of the biggest problems of global health today. In the search for a new class of potential antimicrobial agents, ten new compounds were designed and synthesized based on the quinuclidinium heterocyclic core and the oxime functional group. The antimicrobial activity was assessed against a panel of representative gram-positive and gram-negative bacteria. All compounds demonstrated potent activity against the tested microorganisms, with the minimum inhibitory concentration (MIC) values ranging from 0.25 to 256.00 μg/mL. Among the tested compounds, two quaternary compounds, --chlorobenzyl and --bromobenzyl quinuclidinium oximes, displayed the most potent and broad-spectrum activity against both gram-positive and gram-negative bacterial strains (MIC values from 0.25 to 4.00 μg/mL), with the lowest value for the important multidrug resistant gram-negative pathogen . In the case of , activity of those compounds are 256-fold and 16-fold better than gentamicin, respectively. MTT assays showed that compounds are nontoxic for human cell lines. Multi-way analysis was used to separately reduce dimensionality of quantum chemical data and biological activity data to obtain a regression model and the required parameters for the enhancement of biological activity.

摘要

目前,开发新的抗生素非常重要,因为抗生素耐药性是当今全球健康面临的最大问题之一。在寻找新的一类潜在抗菌剂的过程中,基于奎尼丁杂环核心和肟官能团,设计并合成了十种新的化合物。评估了这些化合物对一组代表性的革兰氏阳性和革兰氏阴性细菌的抗菌活性。所有化合物对测试的微生物均表现出很强的活性,最小抑菌浓度(MIC)值范围为 0.25 至 256.00 μg/mL。在测试的化合物中,两种季铵化合物--氯苄基和--溴苄基奎尼丁肟,对革兰氏阳性和革兰氏阴性细菌菌株均表现出最强和最广谱的活性(MIC 值为 0.25 至 4.00 μg/mL),对重要的多药耐药革兰氏阴性病原体的最低值为. 对于 ,这些化合物的活性分别比庆大霉素好 256 倍和 16 倍。MTT 测定表明,这些化合物对人细胞系没有毒性。多元分析用于分别降低量子化学数据和生物活性数据的维数,以获得增强生物活性的回归模型和所需参数。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7236/6680456/b9c690a76ea0/molecules-24-02675-g001.jpg

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