化学
甲基转移酶
赖氨酸
对偶(语法数字)
药理学
生物化学
癌症研究
甲基化
氨基酸
DNA
医学
艺术
文学类
生物
作者
Chunju Yang,Bang Li,Zongbo Feng,Huaxuan Li,Hong Yang,Zhenjiao Yang,Li Liu,Qiongyu Shi,Hong Wang,Zhong‐Zhu Chen,Xun Huang,Junjian Wang,Yuanxiang Wang
标识
DOI:10.1021/acs.jmedchem.4c00640
摘要
Both G9a and NSD2 have been recognized as promising therapeutic targets for cancer treatment. However, G9a inhibitors only showed moderate inhibitory activity against solid tumors and NSD2 inhibitors were limited to the treatment of hematological malignancies. Inspired by the advantages of dual-target inhibitors that show great potential in enhancing efficiency, we developed a series of highly potent G9a/NSD2 dual inhibitors to treat solid tumors. The candidate
科研通智能强力驱动
Strongly Powered by AbleSci AI