抗真菌
环肽
计算生物学
化学
合理设计
肽
组合化学
合成生物学
模块化设计
生物化学
天然产物
化学生物学
脚手架
生物
生物活性
药物发现
纳米技术
模块化(生物学)
抗真菌药
天然化合物
透视图(图形)
生化工程
生物技术
结构-活动关系
作者
Lexing Zhang,Yue Wang,Qibin Chen,Qi Zhang
标识
DOI:10.1021/acs.jafc.6c01397
摘要
Confronting the escalating threat of drug-resistant invasive fungal infections, cyclic peptides have emerged as a privileged scaffold for next-generation antifungal discovery. Their cyclic architecture confers enhanced metabolic stability, the peptide backbone enables efficient synthetic access, and their modular nature permits systematic structural diversification. This review summarizes recent advances in both natural and synthetic antifungal cyclic peptides, highlighting their biological sources, mechanisms of action, and structure-activity relationships (SAR). By offering an integrated perspective on this evolving chemical class, this work aims to inform the rational design of novel antifungal agents capable of overcoming existing therapeutic limitations.
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