计算机科学
系列(地层学)
计算生物学
组合化学
化学
生物
古生物学
作者
Jingjing Peng,Xiaoyu Ding,Celia Y. Chen,Pei‐Yu Shih,Qingyuan Meng,Xiao Ding,Man Zhang,Alexander Aliper,Feng Ren,Hongfu Lu,Alex Zhavoronkov
标识
DOI:10.1021/acsmedchemlett.4c00434
摘要
Hematopoietic progenitor kinase 1 (HPK1) negatively affects T cell activation and proliferation and is a promising target for immunotherapy. Although HPK1 inhibitors have shown promising efficacy in preclinical models, none have been approved for clinical use. One significant challenge in developing an HPK1 inhibitor is the difficulty in designing a potent inhibitor with good kinase selectivity and pharmacokinetic properties. Here, we report a series of spiro HPK1 inhibitors with good potency and selectivity. Specifically, compound
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