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
中国国家自然科学基金; 国家重点研发计划;
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
相关论文
共 50 条
  • [41] Discovery of a Drug-like, Natural Product-Inspired DCAF11 Ligand Chemotype
    Gang Xue
    Jianing Xie
    Matthias Hinterndorfer
    Marko Cigler
    Lara Dötsch
    Hana Imrichova
    Philipp Lampe
    Xiufen Cheng
    Soheila Rezaei Adariani
    Georg E. Winter
    Herbert Waldmann
    Nature Communications, 14
  • [42] Discovery of a Drug-like, Natural Product-Inspired DCAF11 Ligand Chemotype
    Xue, Gang
    Xie, Jianing
    Hinterndorfer, Matthias
    Cigler, Marko
    Doetsch, Lara
    Imrichova, Hana
    Lampe, Philipp
    Cheng, Xiufen
    Adariani, Soheila Rezaei
    Winter, Georg E.
    Waldmann, Herbert
    NATURE COMMUNICATIONS, 2023, 14 (01)
  • [43] Monomeric Targeted Protein Degraders
    Hanan, Emily J.
    Liang, Jun
    Wang, Xiaojing
    Blake, Robert A.
    Blaquiere, Nicole
    Staben, Steven T.
    JOURNAL OF MEDICINAL CHEMISTRY, 2020, 63 (20) : 11330 - 11361
  • [44] HYDROGENASE ACTIVE SITES: A NEW PARADIGM FOR NATURAL PRODUCT-INSPIRED SYNTHESIS BASED ON ORGANOMETALLIC CHEMISTRY
    Darensbourg, Marcetta Y.
    COMMENTS ON INORGANIC CHEMISTRY, 2010, 31 (3-4) : 144 - 152
  • [45] Natural Product-Inspired Vanadium Pentoxide Nanoparticles Unlock Diabetic Therapeutic Potential: In Vitro and In Silico Evaluation
    Bansal, Smriti
    Tomer, Archana
    Jain, Purnima
    ACS APPLIED BIO MATERIALS, 2025, 8 (03): : 2027 - 2051
  • [46] Divergent Solid-Phase Synthesis of Natural Product-Inspired Bipartite Cyclodepsipeptides: Total Synthesis of Seragamide A
    Arndt, Hans-Dieter
    Rizzo, Stefano
    Noecker, Christina
    Wakchaure, Vijay N.
    Milroy, Lech-Gustav
    Bieker, Vanessa
    Calderon, Abram
    Tran, Tuyen T. N.
    Brand, Silke
    Dehmelt, Leif
    Waldmann, Herbert
    CHEMISTRY-A EUROPEAN JOURNAL, 2015, 21 (14) : 5311 - 5316
  • [47] From Natural Product-Inspired Pyrrolidine Scaffolds to the Development of New Human Golgi α-Mannosidase II Inhibitors
    Cheng, Ting-Jen R.
    Chan, Ting-Hao
    Tsou, En-Lun
    Chang, Shang-Yu
    Yun, Wen-Yi
    Yang, Pei-Jung
    Wu, Ying-Ta
    Cheng, Wei-Chieh
    CHEMISTRY-AN ASIAN JOURNAL, 2013, 8 (11) : 2600 - 2604
  • [48] Convergent Synthesis and Discovery of a Natural Product-Inspired Paralog-Selective Hsp90 Inhibitor
    Jeso, Valer
    Cherry, Lisa
    Macklin, Todd K.
    Pan, Subhas Chandra
    LoGrasso, Philip V.
    Micalizio, Glenn C.
    ORGANIC LETTERS, 2011, 13 (19) : 5108 - 5111
  • [49] Multiple Chemical Features Impact Biological Performance Diversity of a Highly Active Natural Product-Inspired Library
    Hippman, Ryan S.
    Pavlinov, Ivan
    Gao, Qiwen
    Mavlyanova, Michelle K.
    Gerlach, Erica M.
    Aldrich, Leslie N.
    CHEMBIOCHEM, 2020, 21 (21) : 3137 - 3145
  • [50] Synthesis and Evaluation of Marine Natural Product-Inspired Meroterpenoids with Selective Activity toward Dormant Mycobacterium tuberculosis
    Si, Anshupriya
    Landgraf, Alexander D.
    Geden, Sandra
    Sucheck, Steven J.
    Rohde, Kyle H.
    ACS OMEGA, 2022, : 23487 - 23496