Design, synthesis and activity study of a novel PI3K degradation by hijacking VHL E3 ubiquitin ligase

被引:17
|
作者
Wang, Haili [1 ]
Li, Chuchu [1 ]
Liu, Xiaoqing [3 ]
Ma, Mingliang [1 ,2 ]
机构
[1] East China Normal Univ, Shanghai Engn Res Ctr Mol Therapeut & New Drug Dev, Sch Chem & Mol Engn, Shanghai 200062, Peoples R China
[2] East China Normal Univ, Sch Life Sci, Key Lab Brain Funct Genom, Minist Educ, Shanghai 200062, Peoples R China
[3] Shanghai Univ Med & Hlth Sci, Affiliated Zhoupu Hosp, Shanghai 201318, Peoples R China
关键词
PROTAC; PI3K; VHL; Degradation; PROTEOLYSIS-TARGETING CHIMERAS; PATHWAY; INHIBITORS; MOLECULES; PROTEINS; PROTACS; CANCER;
D O I
10.1016/j.bmc.2022.116707
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PI3K kinase plays an important role in regulating key processes in cells, such as cell growth, metabolism, proliferation, and apoptosis. The overexpression of PI3K kinase exists in many cancers. The proteolytic target chimera (PROTAC) technology is a new technology that uses the ubiquitin-proteasome system to degrade a given target protein. It has been described that CRBN-based PROTAC targets the degradation of PI3K kinase. However, PROTAC based on VHL has not been reported yet. Here, we connected the previously obtained highly active PI3K inhibitor to the VHL ligand through different small molecules, and obtained a series of PROTAC molecules targeting PI3K kinase. Obtain the most active compound through screening. It provides evidence for the feasibility of PROTAC technology to recruit VHL E3 ligase in PI3K kinase.
引用
收藏
页数:12
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