萘酰亚胺作为新型多靶点有前景的抗生素结构骨架的全面研究。

IF 3.2 4区 医学 Q3 CHEMISTRY, MEDICINAL
Future medicinal chemistry Pub Date : 2025-03-01 Epub Date: 2025-02-16 DOI:10.1080/17568919.2025.2463872
Lin-Li Mou, Xin-Miao Wu, Aisha Bibi, Jin-Xin Wang, Cheng-He Zhou
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引用次数: 0

摘要

全球范围内不断增长的抗菌素耐药性严重威胁着人类健康,开发新型抗菌素已成为人们关注的焦点。萘酰亚胺含有特殊的环双亚胺骨架和萘骨架,这种独特的结构可以发挥多靶向能力,有助于克服不断升级的耐药性问题。因此,与萘酰亚胺作为新型抗菌剂的开发有关的研究日益活跃。萘酰亚胺作为一种新型的多靶向抗生素结构骨架,不仅具有靶向dna和酶、扰乱膜、产生活性氧等不诱导耐药的多靶向作用,而且具有广泛的抗菌谱,具有安全性和药代动力学特征,通过对萘酰亚胺类抗菌药物的不断研究,预示着萘酰亚胺类抗菌药物作为新型抗生素的巨大潜力。本文综述了萘酰亚胺类抗菌药物的研究现状,并对其合理设计策略、构效关系和作用机制进行了探讨,以期为合理设计高效、广谱、低毒的萘酰亚胺类抗菌药物提供新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A comprehensive insight into naphthalimides as novel structural skeleton of multitargeting promising antibiotics.

The globally growing antimicrobial resistance seriously threatens human health, increasing efforts have been devoting to the development of novel antibiotics. Naphthalimides contain a special skeleton of cyclic double imides and the naphthalene framework, this unique structure can exert multitargeting abilities which are helpful to overcome the escalating issue of resistance. Therefore, research in connection with the development of naphthalimides as novel antimicrobial agents is becoming progressively active. It has been revealed that naphthalimides as novel structural skeleton of multitargeting promising antibiotics could not only target DNAs and enzymes, disturb membrane, produce reactive oxygen species, etc. suggesting the multitargeting actions which do not induce resistance, but also show a broad antimicrobial spectrum with safety profile and pharmacokinetic characteristics, implying large potential as a new type of antibiotics via continuous efforts toward antimicrobial naphthalimides. This review presents naphthalimides as a new type of potential antimicrobial agents and discusses rational design strategies, structure-activity relationships, and mechanisms of action, with a comprehensive view to providing a new insight for in the rational design of efficient, broad-spectrum, and low-toxic naphthalimide antibiotics.

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来源期刊
Future medicinal chemistry
Future medicinal chemistry CHEMISTRY, MEDICINAL-
CiteScore
5.80
自引率
2.40%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Future Medicinal Chemistry offers a forum for the rapid publication of original research and critical reviews of the latest milestones in the field. Strong emphasis is placed on ensuring that the journal stimulates awareness of issues that are anticipated to play an increasingly central role in influencing the future direction of pharmaceutical chemistry. Where relevant, contributions are also actively encouraged on areas as diverse as biotechnology, enzymology, green chemistry, genomics, immunology, materials science, neglected diseases and orphan drugs, pharmacogenomics, proteomics and toxicology.
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