化学
葛兰素史克-3
糖原合酶
GSK3B公司
酶
激酶
酶抑制剂
生物化学
立体化学
作者
Qing Ye,Yanhong Shen,Yubo Zhou,Dan Lv,Jianrong Gao,Jia Li,Yongzhou Hu
标识
DOI:10.1016/j.ejmech.2013.07.046
摘要
A series of 7-azaindazolyl-indolyl-maleimides were designed, synthesized and evaluated for their GSK-3β inhibitory activity. Most compounds exhibited potent activity against GSK-3β. Among them, compounds 17a, 17b, 17g, 17i, 29a and 30 significantly reduced Aβ-induced Tau hyperphosphorylation, showin;g the inhibition of GSK-3β at the cell level. Preliminary structure–activity relationships were discussed based on the experimental data obtained.
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