抗生素
药物开发
药物发现
抗菌活性
抗生素耐药性
抗菌药物
广谱
抗菌剂
抗药性
药品
业务
生物技术
风险分析(工程)
生物
纳米技术
细菌
药理学
微生物学
化学
组合化学
生物信息学
材料科学
遗传学
作者
Roderich D. Süßmuth,Marcel David Kulike-Koczula,Peng Gao,Simone Kosol
出处
期刊:Angewandte Chemie
[Wiley]
日期:2024-11-29
卷期号:64 (10): e202414325-e202414325
被引量:37
标识
DOI:10.1002/anie.202414325
摘要
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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