化学
Cdc25型
药物发现
计算生物学
药品
细胞周期
虚拟筛选
药物重新定位
细胞
药理学
生物化学
生物
细胞周期蛋白依赖激酶1
作者
Yucen Tao,Xia Hao,Xiao Ding,Srinivasulu Cherukupalli,Yuning Song,Xinyong Liu,Peng Zhan
标识
DOI:10.1016/j.ejmech.2020.112374
摘要
Cell division cycle 25 (CDC25) phosphatases, a kind of cell cycle regulators, have become an attractive target for drug discovery, as they have been found to be over-expressed in various human cancer cells. Several CDC25 inhibitors have achieved significant attention in clinical trials with possible mechanistic actions. Prompted by the significance of CDC25 inhibitors with medicinal chemistry prospect, it is an apt time to review the various drug discovery methods involved in CDC25 drug discovery including high throughput screening (HTS), virtual screening (VS), fragment-based drug design, substitution decorating approach, structural simplification approach and scaffold hopping method to seek trends and identify promising new avenues of CDC25 drug discovery.
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