Non-peptidic natural products as ubiquitin-proteasome inhibitors

被引:4
|
作者
Sengupta, Saumitra [1 ]
Mehta, Goverdhan [1 ]
机构
[1] Univ Hyderabad, Sch Chem, Hyderabad 5000046, Telangana, India
关键词
Ubiquitin; Proteasome; Deubiquitinases; Inhibitor; Anti-cancer; Natural products; Total synthesis; Medicinal chemistry; Drug discovery; PROTEIN-PROTEIN INTERACTION; ENANTIOSELECTIVE TOTAL-SYNTHESIS; SMALL-MOLECULE INHIBITORS; ACTIVITY IN-VITRO; 20; S-PROTEASOME; CATALYTIC ASYMMETRIC-SYNTHESIS; ACTIVATING ENZYME-INHIBITOR; PUMMERER REACTION CHEMISTRY; KITASATOSPORA SP MK993-DF2; EFFICIENT TOTAL-SYNTHESIS;
D O I
10.1016/j.tet.2018.12.012
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Approval of bortezomib has validated ubiquitin-proteasome pathway as an important target for treatment of haematological malignancies. However, clinical shortcomings of bortezomib, a covalent peptide proteasome inhibitor, has prompted a paradigm shift in anti-proteasome drug discovery towards development of non-peptidic inhibitors and targeting of upstream ubiquitin system which has drawn traction for interdisciplinary forays. It is being widely recognized that natural products provide valuable leads in the discovery of potent, chemically diverse, non-peptidic inhibitors of 20S proteasome and of key enzymes involved in ubiquitination machinery. As a result, total synthesis of natural, non-peptidic inhibitors of ubiquitin-proteasome pathway has emerged as a critical interlink between organic synthesis, medicinal chemistry, biochemical profiling and drug discovery. An up-to-date account of contextual synthetic challenges, strategies and accomplishments as well as mapping of the chemical diversity space around the natural scaffolds has been captured in this review. (C) 2018 Published by Elsevier Ltd.
引用
收藏
页码:817 / 853
页数:37
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