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喹啉腙衍生物作为新型抗菌药物对抗多重耐药菌株。

Quinoline Hydrazone Derivatives as New Antibacterials against Multidrug Resistant Strains.

机构信息

V.P. Kukhar Institute of Bioorganic Chemistry and Petrochemistry of, National Academy of Science of Ukraine, Kyiv, 02094, Academician Kukhar Str., 1, Ukraine.

Zaporizhzhya National University, Faculty of Biology, Zaporizhzhya, 69095, Zhukovs'ky Str., 66, Ukraine.

出版信息

Chem Biodivers. 2023 Sep;20(9):e202300839. doi: 10.1002/cbdv.202300839. Epub 2023 Aug 28.

Abstract

To develop novel antimicrobial agents a series of 2(4)-hydrazone derivatives of quinoline were designed, synthesized and tested. QSAR models of the antibacterial activity of quinoline derivatives were developed by the OCHEM web platform using different machine learning methods. A virtual set of quinoline derivatives was verified with a previously published classification model of anti-E. coli activity and screened using the regression model of anti-S. aureus activity. Selected and synthesized 2(4)-hydrazone derivatives of quinoline exhibited antibacterial activity against the standard and antibiotic-resistant S. aureus and E. coli strains in the range from 15 to 30 mm by the diameter of growth inhibition zones. Molecular docking showed the complex formation of the studied compounds into the catalytic domain of dihydrofolate reductase with an estimated binding affinity from -8.4 to -9.4 kcal/mol.

摘要

为了开发新型抗菌剂,设计、合成并测试了一系列喹啉的 2(4)-腙衍生物。利用 OCHEM 网络平台,采用不同的机器学习方法,建立了喹啉衍生物的抗菌活性定量构效关系模型。利用先前发表的抗大肠杆菌活性分类模型对一组虚拟喹啉衍生物进行了验证,并利用抗金黄色葡萄球菌活性的回归模型进行了筛选。选择并合成的 2(4)-腙衍生物对标准和抗生素耐药的金黄色葡萄球菌和大肠杆菌菌株的抑菌圈直径范围为 15-30 mm,表现出抗菌活性。分子对接表明,研究化合物与二氢叶酸还原酶的催化结构域形成复合物,估计结合亲和力为-8.4 到-9.4 kcal/mol。

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