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
{"title":"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","authors":"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","doi":"10.1016/j.ejmech.2025.117387","DOIUrl":null,"url":null,"abstract":"<div><div>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 <em>Acinetobacter baumannii</em> (<em>A</em>. <em>baumannii</em>) and <em>Escherichia coli</em> (<em>E. coli</em>). Compound <strong>4a</strong> significantly synergized polymyxin B in combating <em>A. baumannii</em> and <em>E</em>. <em>coli</em> both <em>in vitro</em> and on the infected <em>Galleria mellonella</em> models. Furthermore, we identified <strong>4a</strong> 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.</div></div>","PeriodicalId":314,"journal":{"name":"European Journal of Medicinal Chemistry","volume":"289 ","pages":"Article 117387"},"PeriodicalIF":5.9000,"publicationDate":"2025-05-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Pyrylium derivatives as outer membrane permeabilizers against MDR gram-negative bacteria via multi-target mode of action\",\"authors\":\"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\",\"doi\":\"10.1016/j.ejmech.2025.117387\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>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 <em>Acinetobacter baumannii</em> (<em>A</em>. <em>baumannii</em>) and <em>Escherichia coli</em> (<em>E. coli</em>). Compound <strong>4a</strong> significantly synergized polymyxin B in combating <em>A. baumannii</em> and <em>E</em>. <em>coli</em> both <em>in vitro</em> and on the infected <em>Galleria mellonella</em> models. Furthermore, we identified <strong>4a</strong> 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.</div></div>\",\"PeriodicalId\":314,\"journal\":{\"name\":\"European Journal of Medicinal Chemistry\",\"volume\":\"289 \",\"pages\":\"Article 117387\"},\"PeriodicalIF\":5.9000,\"publicationDate\":\"2025-05-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Medicinal Chemistry\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0223523425001527\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/2/18 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0223523425001527","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/18 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
Pyrylium derivatives as outer membrane permeabilizers against MDR gram-negative bacteria via multi-target mode of action
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.
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.