Actinomycetes: Treasure trove for discovering novel antibiotic candidates

IF 5.9 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2025-01-25 DOI:10.1016/j.ejmech.2025.117317
Rexing Yi , Yutong Shi , Xun Cao , Chengqian Pan
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Abstract

Actinomycetes are an important source of secondary metabolites such as antibiotics and other active natural products. Many well-known antibiotics, such as streptomycin, oxytetracycline, and tetracycline, are produced by actinomycetes. Different types of antibiotics have distinct mechanisms of action against microorganisms: inhibit protein synthesis, inhibit nucleic acid synthesis, or inhibit cell wall synthesis. For decades, actinomycetes have played a crucial role in clinical treatment for major diseases such as pathogenic bacterial infections, serving as one of the most significant sources of new discoveries. However, due to extensive use of antibiotics, the types and numbers of drug-resistant bacteria, represented by multidrug resistant (MDR) and extensively drug resistant (XDR) bacteria, have increased dramatically in clinical settings, posing a significant threat to human survival. Therefore, there is an urgent need to search for structurally novel antibacterial natural products and develop new antibiotics. In this review, a total of 170 antibacterial secondary metabolites from actinomycetes, published in the 54 literatures (2020 to September 2024) and some synthetic analogs, are discussed with emphasis on their structures and biological activities.

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放线菌:发现新型抗生素候选物的宝库
放线菌是次生代谢物如抗生素和其他活性天然产物的重要来源。许多众所周知的抗生素,如链霉素、土霉素和四环素,都是由放线菌产生的。不同类型的抗生素对微生物有不同的作用机制:抑制蛋白质合成,抑制核酸合成,或抑制细胞壁合成。几十年来,放线菌在病原菌感染等重大疾病的临床治疗中发挥了至关重要的作用,是新发现的最重要来源之一。然而,由于抗生素的广泛使用,以多重耐药(MDR)和广泛耐药(XDR)细菌为代表的耐药细菌的种类和数量在临床环境中急剧增加,对人类生存构成重大威胁。因此,迫切需要寻找结构新颖的抗菌天然产物,开发新型抗生素。本文综述了从2020年至2024年9月共发表的54篇文献中发现的170种放线菌抗菌次生代谢物及其合成类似物,重点介绍了它们的结构和生物活性。
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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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