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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:
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
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页码:586 / 592
页数:7
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