发现自然存在的循环抗菌及其结构优化策略
Ping Zeng1, Honglan Wang1, Pengfei Zhang1
1School of Pharmacy, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, Hong Kong.
Biotechnology advances
|May 4, 2024
概括
在过去十年中发现的新型循环抗菌 (CABPs) 对抗多药耐药细菌提供了有希望的解决方案. 本综述强调了它们的结构,机制和作为下一代抗生素的潜力.
科学领域:
- 微生物学和天然产品化学
- 药物发现和开发 药物发现和开发
背景情况:
- 多抗药性 (MDR) 细菌对全球健康构成威胁,需要新的抗菌剂.
- 循环抗菌 (CABPs) 与线性对应物相比,显示出增强的稳定性和杀菌作用.
- 现有的基于CABP的抗生素面临着新兴的耐药性,推动了对新疗法选择的需求.
研究的目的:
- 审查过去十年发现的新型自然存在的CABPs.
- 根据化学结构对CABP进行分类,并讨论其特性.
- 分析工程 CABP 类型的结构-活动关系.
主要方法:
- 在过去的10年中,对自然发生的CABPs的文献综述.
- 将CABP分为五个结构组:乳/乳基,循环脂,糖,循环富硫和多次修改的CABP.
- 讨论化学结构,抗菌光谱,拟议的机制和工程类型.
主要成果:
- 鉴定和分类具有显著抗菌活性的新型CABP.
- 对CABP的五个不同的结构类别进行了详细分析.
- 工程 CABP 类似物和初步结构-活动关系见解的总结.
结论:
- 新型CABP代表了对抗MDR细菌感染的有希望的途径.
- 衍生设计有效地识别来自新型CABP的强效抗菌剂.
- 对CABP的持续研究对于解决全球抗生素耐药性危机至关重要.
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