Yan Xiaohui
State Key Laboratory of Component-based Chinese Medicine, Tianjin University of Traditional Chinese Medicine, 10 Poyanghu Road, West Area, Tuanbo New Town, Jinghai District, Tianjin, China.
Nat Prod Rep. 2022 Mar 23;39(3):703-728. doi: 10.1039/d1np00054c.
Covering: up to the end of July, 2021Anthraquinone-fused enediynes (AFEs) are a subfamily of enediyne natural products. Dynemicin A (DYN A), the first member of the AFE family, was discovered more than thirty years ago. Subsequently, extensive studies have been reported on the mode of action and the interactions of AFEs with DNA using DYN A as a model. However, progress in the discovery, biosynthesis and clinical development of AFEs has been limited for a long time. In the past five years, four new AFEs have been discovered and significant progress has been made in the biosynthesis of AFEs, especially on the biogenesis of the anthraquinone moiety and their tailoring steps. Moreover, the streamlined total synthesis of AFEs and their analogues boosts the preparation of AFE-based linker-drugs, thus enabling the development of AFE-based antibody-drug conjugates (ADCs). This review summarizes the discovery, mechanism of action, biosynthesis, total synthesis and preclinical studies of AFEs.
截至2021年7月底
蒽醌稠合烯二炔(AFEs)是烯二炔天然产物的一个亚家族。达尼霉素A(DYN A)是AFE家族的首个成员,于三十多年前被发现。随后,以DYN A为模型,对AFEs的作用方式以及它们与DNA的相互作用进行了广泛研究。然而,长期以来,AFEs在发现、生物合成和临床开发方面进展有限。在过去五年中,已发现四种新的AFEs,并且在AFEs的生物合成方面取得了重大进展,特别是在蒽醌部分的生物合成及其修饰步骤方面。此外,AFEs及其类似物的简化全合成促进了基于AFE的连接体药物的制备,从而推动了基于AFE的抗体药物偶联物(ADCs)的开发。本综述总结了AFEs的发现、作用机制、生物合成、全合成及临床前研究。