KEAP1型
化学
转录因子
小分子
药物发现
蛋白质-蛋白质相互作用
核蛋白
药物开发
血浆蛋白结合
药品
生物化学
细胞生物学
计算生物学
药理学
生物
基因
作者
Ziquan Zhao,Ruitian Dong,Qidong You,Zhengyu Jiang
标识
DOI:10.1021/acs.jmedchem.3c00712
摘要
Oxidative stress has been implicated in a wide range of pathological conditions. The transcription factor nuclear factor erythroid 2-related factor 2 (Nrf2) exerts a central role in regulating the cellular defense system against oxidative and electrophilic insults. Nonelectrophilic inhibition of the protein–protein interaction (PPI) between Kelch-like ECH-associated protein 1 (Keap1) and Nrf2 has become a promising approach to activate Nrf2. Recently, multiple drug discovery strategies have facilitated the development of small-molecule Keap1–Nrf2 PPI inhibitors with potent activity and favorable drug-like properties. In this Perspective, we summarize the latest progress of small-molecule Keap1–Nrf2 PPI inhibitors from medicinal chemistry insights and discuss future prospects and challenges in this field.
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