Pyrylium derivatives as outer membrane permeabilizers against MDR gram-negative bacteria via multi-target mode of action

IF 5.9 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2025-05-05 Epub Date: 2025-02-18 DOI:10.1016/j.ejmech.2025.117387
Qionglu Duan , Min Yuan , Xican Ma , Yifan Zheng , Runze Meng , Wenjing Shi , Yanan Ni , Chen Zhao , Yonghua Liu , Zhihui Yu , Jingyang Zhu , Yulong Shi , Xi Zhu , Li Li , Shuyi Si , Yan Li , Yinghong Li , Danqing Song
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Abstract

The prevalence of MDR Gram-negative bacteria has posed a great impetus for the discovery of new therapeutic approaches. Here, we synthesized a series of pyrylium derivatives as antibiotic adjuvants based on IMB-0042, and evaluated their activities against Acinetobacter baumannii (A. baumannii) and Escherichia coli (E. coli). Compound 4a significantly synergized polymyxin B in combating A. baumannii and E. coli both in vitro and on the infected Galleria mellonella models. Furthermore, we identified 4a to be an effective perturbant of the Gram-negative outer membrane (OM) through the blockage on LptA/LptC interaction via targeting Met47 in LptA. And cationic pyrylium reduced the OM densification by electrostatic interaction with anion-rich lipopolysaccharide (LPS). Thus, pyrylium derivatives constitute a new class of multi-target OM permeabilizers, which can significantly potentiate antibiotics against MDR Gram-negative bacteria.

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吡啶衍生物作为耐多药革兰氏阴性菌外膜渗透剂的多靶点作用模式
耐多药革兰氏阴性菌的流行为发现新的治疗方法提供了巨大的推动力。本研究以IMB-0042为基础合成了一系列吡啶衍生物作为抗生素佐剂,并对其抗鲍曼不动杆菌(a . baumannii)和大肠杆菌(E. coli)的活性进行了评价。化合物4a与多粘菌素B在体外和受感染的mellonella模型上均具有显著的协同作用,可对抗鲍曼不动杆菌和大肠杆菌。此外,我们发现4a通过靶向LptA中的Met47阻断LptA/LptC相互作用,从而有效地干扰了革兰氏阴性外膜(OM)。阳离子吡啶通过与富阴离子脂多糖(LPS)的静电相互作用降低了OM的致密化。因此,吡啶衍生物构成了一类新的多靶点OM渗透剂,可以显著增强抗生素对耐多药革兰氏阴性菌的作用。
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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