Natural Product-Inspired Targeted Protein Degraders: Advances and Perspectives

被引:20
作者
Li, Jiao [1 ,2 ]
Cai, Zhenyu [3 ]
Li, Xu-Wen [4 ,5 ]
Zhuang, Chunlin [1 ,2 ]
机构
[1] Tongji Univ, Shanghai Peoples Hosp 10, Clin Med Sci & Tech Innovat Ctr, Sch Med, Shanghai 200072, Peoples R China
[2] Second Mil Med Univ, Sch Pharm, Shanghai 200433, Shanghai, Peoples R China
[3] Tongji Univ, Tongji Univ Canc Ctr, Shanghai Peoples Hosp 10, Sch Med, Shanghai 200092, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, Shanghai 201203, Peoples R China
[5] Bohai Rim Adv Res Inst Drug Discovery, Shandong Lab Yantai Drug Discovery, Yantai 264117, Shandong, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
PSEUDOLARIC ACID-B; ARYL-HYDROCARBON RECEPTOR; SMALL MOLECULES; RETINOIC-ACID; BARDOXOLONE METHYL; CHIMERIC MOLECULES; CELL-DEATH; DEGRADATION; DESIGN; DISCOVERY;
D O I
10.1021/acs.jmedchem.2c01223
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Targeted protein degradation (TPD), a promising therapeutic strategy in drug discovery, has great potential to regulate the endogenous degradation of undruggable targets with small molecules. As vital resources that provide diverse structural templates for drug discovery, natural products (NPs) are a rising and robust arsenal for the development of therapeutic TPD. The first proof-of-concept study of proteolysis-targeting chimeras (PROTACs) was a natural polyketide ovalicin-derived degrader; since then, NPs have shown great potential to promote TPD technology. The use of NP-inspired targeted protein degraders has been confirmed to be a promising strategy to treat many human conditions, including cancer, inflammation, and nonalcoholic fatty liver disease. Nevertheless, the development of NP-inspired degraders is challenging, and the field is currently in its infancy. In this review, we summarize the bioactivities and mechanisms of NP-inspired degraders and discuss the associated challenges and future opportunities in this field.
引用
收藏
页码:13533 / 13560
页数:28
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