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评价具有香豆素骨架的酶衍生α-氨基膦酸酯对医院病原体的抗菌活性。

Evaluation of Antibacterial Activity against Nosocomial Pathogens of an Enzymatically Derived α-Aminophosphonates Possessing Coumarin Scaffold.

机构信息

Department of Animal Nutrition, The Kielanowski Institute of Animal Physiology and Nutrition, Polish Academy of Sciences, Instytucka 3, 05-110 Jabłonna, Poland.

Institute of Organic Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.

出版信息

Int J Mol Sci. 2023 Oct 4;24(19):14886. doi: 10.3390/ijms241914886.

Abstract

The purpose of the present study was to evaluate the synergistic effect of two important pharmacophores, coumarin and α-amino dimethyl phosphonate moieties, on antimicrobial activity against selected strains of multidrug-resistant nosocomial pathogenic bacteria. The previously developed enzyme-catalysed Kabachnik-Fields protocol allowed us to obtain the studied compounds with high yields which were free from metal impurities. The structure-activity relationship revealed that inhibitory activity is strongly related to the presence of the trifluoromethyl group (CF-) in the coumarin scaffold. MIC and MBC studies carried out on six selected pathogenic bacterial strains (Gram-positive pathogenic (ATCC 23235) strain, as well as on Gram-negative (ATCC 17978), (ATCC 15442), (ATCC 49141), (ATCC 33277), and (ATCC 35405)) have shown that tested compounds show a strong bactericidal effect at low concentrations. Among all agents investigated, five exhibit higher antimicrobial activity than those observed for commonly used antibiotics. It should be noted that all the compounds tested showed very high activity against , which is the main source of nosocomial infections that cause numerous fatalities. Furthermore, we have shown that the studied coumarin-based α-aminophosphonates, depending on their structural characteristics, are non-selective and act efficiently against various Gram-positive and Gram-negative pathogens, which is of great importance for hospitalised patients.

摘要

本研究的目的是评估香豆素和α-氨基二甲基膦酸酯两个重要药效团的协同作用对所选多药耐药医院病原体的抗菌活性。先前开发的酶催化 Kabachnik-Fields 方案使我们能够以高产率获得研究化合物,且无金属杂质。结构-活性关系表明,抑制活性与香豆素支架中三氟甲基(CF-)的存在密切相关。对六种选定的致病性细菌菌株(革兰氏阳性致病性(ATCC 23235)菌株以及革兰氏阴性(ATCC 17978)、(ATCC 15442)、(ATCC 49141)、(ATCC 33277)和(ATCC 35405))进行的 MIC 和 MBC 研究表明,测试化合物在低浓度下表现出很强的杀菌作用。在所研究的所有药物中,有五种表现出比常用抗生素更高的抗菌活性。值得注意的是,所有测试的化合物对 表现出非常高的活性,这是导致许多死亡的医院感染的主要病原体。此外,我们已经表明,所研究的基于香豆素的α-氨基膦酸酯根据其结构特征是非选择性的,对各种革兰氏阳性和革兰氏阴性病原体有效,这对住院患者非常重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b6/10574003/a750b6f1b719/ijms-24-14886-g001.jpg

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