Fighting Antimicrobial Resistance: Innovative Drugs in Antibacterial Research

IF 16.9 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY Angewandte Chemie International Edition Pub Date : 2024-11-29 DOI:10.1002/anie.202414325
Roderich D. Süssmuth, Marcel Kulike-Koczula, Peng Gao, Simone Kosol
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Abstract

In the fight against bacterial infections, particularly those caused by multi-resistant pathogens known as “superbugs”, the need for new antibacterials is undoubted in scientific communities and is by now also widely perceived by the general population. However, the antibacterial research landscape has changed considerably over the past years. With few exceptions, the majority of big pharma companies has left the field and thus, the decline in R&D on antibacterials severely impacts the drug pipeline. In recent years, antibacterial research has increasingly relied on smaller companies or academic research institutions, which mostly have only limited financial resources, to carry a drug discovery and development process from the beginning and through to the beginning of clinical phases. This review formulates the requirements for an antibacterial in regard of targeted pathogens, resistance mechanisms and drug discovery. Strategies are shown for the discovery of new antibacterial structures originating from natural sources, by chemical synthesis and more recently from artificial intelligence approaches. This is complemented by principles for the computer-aided design of antibacterials and the refinement of a lead structure. The second part of the article comprises a compilation of antibacterial molecules classified according to bacterial target structures, e.g. cell wall synthesis, protein synthesis, as well as more recently emerging target classes, e.g. fatty acid synthesis, proteases and membrane proteins. Aspects of the origin, the antibacterial spectrum, resistance and the current development status of the presented drug molecules are highlighted.

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抗微生物药物耐药性:抗菌药物研究中的创新药物
在与细菌感染的斗争中,特别是由多重耐药病原体引起的细菌感染,科学界对新型抗菌药物的需求是毋庸置疑的。现在也被普通大众广泛接受。然而,抗菌研究领域在过去几年中发生了很大的变化。大多数大型制药公司已经离开了这个领域,因此,抗菌药研发的下降严重影响了药物管道。在过去的几年里,抗菌药物研究越来越依赖于小型公司或学术研究机构,这些公司或学术研究机构大多只有有限的资金资源,从开始到临床阶段进行药物发现和开发过程。本文综述了抗菌药物在靶向病原菌和耐药机制方面的要求。策略显示了发现新的抗菌结构源自天然来源,化学合成和最近的人工智能方法。这是补充原则的计算机辅助设计的抗菌剂和细化的铅结构。文章的第二部分包括根据细菌靶区分类的有前途的抗菌分子的汇编。重点介绍了所提药物分子的来源、抗菌谱、耐药性以及目前的发展现状。
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来源期刊
CiteScore
26.60
自引率
6.60%
发文量
3549
审稿时长
1.5 months
期刊介绍: Angewandte Chemie, a journal of the German Chemical Society (GDCh), maintains a leading position among scholarly journals in general chemistry with an impressive Impact Factor of 16.6 (2022 Journal Citation Reports, Clarivate, 2023). Published weekly in a reader-friendly format, it features new articles almost every day. Established in 1887, Angewandte Chemie is a prominent chemistry journal, offering a dynamic blend of Review-type articles, Highlights, Communications, and Research Articles on a weekly basis, making it unique in the field.
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