辅活化剂
计算生物学
配体(生物化学)
化学
虚拟筛选
药物发现
受体
生物信息学
立体化学
组合化学
生物化学
生物
基因
转录因子
作者
Tsuyoshi Shinozuka,Shuichiro Ito,Takako Kimura,Masanori Izumi,Kenji Wakabayashi
标识
DOI:10.1021/acsmedchemlett.1c00100
摘要
A novel class of estrogen-related receptor α (ERRα) agonists has been discovered. A structure–activity relationship study of high-throughput screening hits 1 and 2 led to the discovery of benzimidazole 3d (DS20362725) and acetophenone analogue 5c (DS45500853). The X-ray crystal structure of the ERRα ligand-binding domain in complex with 5c and PGC-1α coactivator peptide revealed conformational changes in the ligand-binding pocket to accommodate 5c and the key interaction between the protein and ligand. Since both analogues avoided PPARγ transcriptional activity, they can be useful tool compounds for investigating biological ERRα functions.
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