虚拟筛选
葛兰素史克-3
化学
神经保护
结构相似性
结构-活动关系
药物发现
计算生物学
糖原合酶
IC50型
激酶
GSK3B公司
酶
药理学
生物化学
体外
生物
作者
Xiaodong Dou,Lan Jiang,Yanxing Wang,Hongwei Jin,Zhenming Liu,Liangren Zhang
标识
DOI:10.1016/j.bmcl.2017.11.036
摘要
Glycogen synthase kinase-3β (GSK-3β) is an attractive therapeutic target for human diseases, such as diabetes, cancer, neurodegenerative diseases, and inflammation. Thus, structure-based virtual screening was performed to identify novel scaffolds of GSK-3β inhibitors, and we observed that conserved water molecules of GSK-3β were suitable for virtual screening. We found 14 hits and D1 (IC50 of 0.71 μM) were identified. Furthermore, the neuroprotection activity of D1–D3 was validated on a cellular level. 2D similarity searches were used to find derivatives of high inhibitory compounds and an enriched structure–activity relationship suggested that these skeletons were worthy of study as potent GSK-3β inhibitors.
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