蛋白酶
计算生物学
药物开发
基因亚型
人类健康
药理学
癌症
医学
生物信息学
药品
生物
化学
生物化学
酶
内科学
基因
环境卫生
作者
Hang Li,Leyuan Chen,Yiliang Li,Wenbin Hou
标识
DOI:10.1080/13543776.2022.2165910
摘要
The available complex crystal structures of SENP1-SUMO1, afforded structure-based drug design opportunities, which led to the development of various isoform-selective small molecule inhibitors belonging to diverse classes (derivatives of benzamides, naphthalenesulfonic acids, pyridones, and the like). Preclinical studies have initially shown the potential advantages of these compounds, which have certain significance for the development of anticancer drugs.
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