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新型补骨脂素衍生物的合成及抗耐甲氧西林金黄色葡萄球菌(MRSA)活性评价。

Synthesis and Antibacterial Evaluation of Novel Psoralen Derivatives against Methicillin-Resistant Staphylococcus aureus (MRSA).

机构信息

School of Chemical and Environmental Engineering, Shanghai Institute of Technology, 100 Haiquan Road, Shanghai, 201418, The People's Republic of China.

School of Pharmacy, Second Military Medical University, 325 Guohe Road, Shanghai, 200433, the People's Republic of China.

出版信息

Chem Biodivers. 2024 Aug;21(8):e202302048. doi: 10.1002/cbdv.202302048. Epub 2024 Feb 12.

Abstract

Today, the bacterial infections caused by multidrug-resistant pathogens seriously threaten human health. Thereby, there is an urgent need to discover antibacterial drugs with novel mechanism. Here, novel psoralen derivatives had been designed and synthesized by a scaffold hopping strategy. Among these targeted twenty-five compounds, compound ZM631 showed the best antibacterial activity against methicillin-resistant S. aureus (MRSA) with the low MIC of 1 μg/mL which is 2-fold more active than that of the positive drug gepotidacin. Molecular docking study revealed that compound ZM631 fitted well in the active pockets of bacterial S. aureus DNA gyrase and formed a key hydrogen bond binding with the residue ASP-1083. These findings demonstrated that the psoralen scaffold could serve as an antibacterial lead compound for further drug development against multidrug-resistant bacterial infections.

摘要

如今,由多重耐药病原体引起的细菌感染严重威胁着人类健康。因此,迫切需要发现具有新型作用机制的抗菌药物。在这里,通过一种基于结构的药物设计方法,设计并合成了新型补骨脂素衍生物。在这 25 个目标化合物中,化合物 ZM631 对耐甲氧西林金黄色葡萄球菌(MRSA)表现出最好的抗菌活性,MIC 值低至 1 μg/mL,比阳性药物 gepotidacin 活性高 2 倍。分子对接研究表明,化合物 ZM631 很好地适应了细菌金黄色葡萄球菌 DNA 拓扑异构酶的活性口袋,并与残基 ASP-1083 形成了关键氢键结合。这些发现表明补骨脂素骨架可以作为进一步开发针对多重耐药细菌感染的抗菌先导化合物。

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