车站3
转录因子
计算生物学
药物开发
信号转导
药物发现
生物
癌症研究
化学
细胞生物学
生物信息学
药品
药理学
遗传学
基因
作者
Rui Wang,Xinyu Cao,Guo‐Qiang Lin,Ping Tian,Dingding Gao
标识
DOI:10.1080/13543776.2022.2056013
摘要
Since the X-ray crystal structure of STAT3β homo dimer bound to DNA was solved in 1998, the development of STAT3 inhibitors has gone through a boom in recent years. However, none of them have been approved for marketing, probably due to the complex biological functions of the STAT3 signaling pathway, including its character and the poor drug-like physicochemical properties of its inhibitors. Nonetheless, targeting STAT3 continues to be an exciting field for the development of anti-tumor agents along with the emergence of new STAT3 inhibitors with unique mechanisms of action.
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