封锁
癌症治疗
免疫系统
癌症
联合疗法
计算生物学
合理设计
医学
癌症治疗
免疫疗法
免疫检查点
逃避(道德)
药物发现
免疫学
生物信息学
药理学
PD-L1
后天抵抗
化学
临床试验
信号通路
受体
癌症研究
铅(地质)
作者
Lili Wang,Hao Shen,Binjian Jiang,Xiao Wang,Peng Yang,Chengliang Sun
标识
DOI:10.1021/acs.jmedchem.5c02693
摘要
Although immune checkpoint blockade therapies targeting PD-1/PD-L1 and CTLA-4 have achieved remarkable clinical success, limitations such as low response rates and acquired resistance remain significant challenges. TIM-3 has recently emerged as a key immunosuppressive receptor and a promising therapeutic target for augmenting antitumor immunity. However, the development of TIM-3 inhibitors is highly imbalanced: multiple antibody-based candidates have entered Phase III trials, whereas small-molecule inhibitors are still in the preclinical stage, with current research remaining fragmented and lacking systematic structure-activity relationship studies. This Account systematically summarizes the structural and functional mechanisms of TIM-3, with a focus on recent advances in the discovery and development of small-molecule TIM-3 inhibitors. We highlight representative lead compounds identified through virtual screening and rational design and discuss future directions to facilitate the development of novel TIM-3-targeted agents.
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