溴尿嘧啶
医学
药效团
癌症
药品
BRD4
疾病
生物
生物信息学
计算生物学
药理学
内科学
组蛋白
生物化学
基因
作者
Sitao Zhang,Yanzhao Chen,Chengsen Tian,Yujing He,Zeru Tian,Yichao Wan,Tingting Liu
标识
DOI:10.2174/0929867327666200610174453
摘要
Developing new anti-cancer agents with new scaffolds and high efficiency is a big challenge for researchers. Dual-target inhibitors based on BRD4 are a class of important bioactive compounds. Making structural modifications on the active dual-target inhibitors according to the corresponding structure-activity relationships is of benefit to obtain more potent anti-cancer leads or clinical drugs. This review will be useful for further development of new dual-target inhibitors based on BRD4 as anti-cancer agents.
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