化学
胶质瘤
突变体
IDH1
药理学
对偶(语法数字)
癌症研究
计算生物学
生物化学
医学
基因
生物
文学类
艺术
作者
Fei Wen,Gang Gui,Xiaoyu Wang,Anqi X. Qin,Tianfang Ma,Hui Chen,Chunzheng Li,Xiaoming Zha
标识
DOI:10.1021/acs.jmedchem.3c02482
摘要
The targeting of cancer cell intrinsic metabolism has emerged as a promising strategy for antitumor intervention. In the study, we identified the first-in-class small molecules that effectively inhibit both mutant isocitrate dehydrogenase 1 (mIDH1) and nicotinamide phosphoribosyltransferase (NAMPT), two crucial targets in cancer metabolism, through structure-based drug design. Notably, compound
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