Design, Synthesis, and Evaluation of PD-1/PD-L1 Antagonists Bearing a Benzamide Scaffold

被引:19
|
作者
Lu, Lu [1 ,2 ]
Qi, Zhihao [1 ,2 ]
Wang, Tianyu [1 ,2 ]
Zhang, Xiangyu [1 ,2 ]
Zhang, Kuojun [1 ,2 ]
Wang, Kaizhen [1 ,2 ]
Cheng, Yao [1 ,2 ]
Xiao, Yibei [1 ,2 ]
Li, Zheng [3 ]
Jiang, Sheng [1 ,2 ]
机构
[1] China Pharmaceut Univ, Dept Med Chem, State Key Lab Nat Med, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Dept Biomed Engn, Nanjing 210009, Peoples R China
[3] Houston Methodist Res Inst, Ctr Bioenerget, Houston, TX 77030 USA
来源
ACS MEDICINAL CHEMISTRY LETTERS | 2022年 / 13卷 / 04期
基金
中国国家自然科学基金;
关键词
PD-L1; inhibitor; PD-1; immune checkpoint; small molecules inhibitors; BIOLOGICAL EVALUATION;
D O I
10.1021/acsmedchemlett.1c00646
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Several antibodies targeting programmed cell death-1 (PD-1)/programmed cell death-ligand 1 (PD-L1) have beenapproved by the U.S. Food and Drug Administration (FDA) forcancer therapy. Although many small-molecule inhibitors of thePD-1/PD-L1 pathway have been reported, no small-moleculeinhibitors have been approved for cancer treatment. In this work, aseries of novel benzamide derivatives were designed, synthesized,and evaluated tofind effective inhibitors of the PD-1/PD-L1interaction. The most potent compoundD2exhibited betteractivity than that of BMS202, with an IC50of 16.17 nM.D2couldactivate the antitumor immunity of T cells efficiently in PBMCs. The proposed binding mode of compoundD2was investigated bydocking analysis. These results indicate that compoundD2is a promising lead compound that can be used for further development
引用
收藏
页码:586 / 592
页数:7
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