Polo样激酶
PLK1
激酶
药物开发
蛋白激酶结构域
计算生物学
生物
药品
细胞
细胞生物学
生物化学
药理学
细胞周期
基因
突变体
作者
Shirong Bian,Ru Zhang,Jianyu Nie,Mingxing Zhu,Zhouling Xie,Chenzhong Liao,Qin Wang
标识
DOI:10.1080/13543776.2024.2379924
摘要
After two decades of drug development on PLKs, several drugs progressed into clinical trials for the treatment of many cancers; however, none of them has been approved yet. Further elucidating the mechanisms of PLKs and identifying and developing highly selective ATP-competitive inhibitors, highly potent drug-like PBD inhibitors, degraders, etc. may provide new opportunities for cancer therapy and the treatment for several nononcologic diseases. PLKs inhibition-based combination therapies can be another helpful strategy.
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