Ecto-nucleotide pyrophosphatase/phosphodiesterase 1 inhibitors: Research progress and prospects

被引:4
|
作者
Guan, Dezhong [2 ]
Fang, Lincheng [4 ]
Feng, Mingshun [3 ]
Guo, Shi [1 ]
Xie, Lingfeng [1 ]
Chen, Chao [1 ]
Sun, Xue [2 ]
Wu, Qingyun [1 ]
Yuan, Xinrui [1 ]
Xie, Zuoquan [3 ]
Zhou, Jinpei [2 ]
Zhang, Huibin [1 ]
机构
[1] China Pharmaceut Univ, Ctr Drug Discovery, State Key Lab Nat Med, 24 Tongjiaxiang, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Dept Med Chem, Tongjiaxiang 24, Nanjing 210009, Peoples R China
[3] Chinese Acad Sci, Div Antitumor Pharmacol, State Key Lab Drug Res, Shanghai Inst Mat Med, Shanghai, Peoples R China
[4] Peking Univ, Shenzhen Grad Sch, Shenzhen, Peoples R China
关键词
ENPP1; inhibitors; cGAS-STING pathway; 2; 3; '-cGAMP; Tumor immunotherapy; INSULIN-RECEPTOR INHIBITOR; ANTICANCER AGENT SULOFENUR; CANCER; ENPP1; NPP1; DERIVATIVES; MEMBRANE; POTENT; RAT; MINERALIZATION;
D O I
10.1016/j.ejmech.2024.116211
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The cancer immunotherapies involved in cGAS-STING pathway have been made great progress in recent years. STING agonists exhibit broad-spectrum anti-tumor effects with strong immune response. As a negative regulator of the cGAS-STING pathway, ecto-nucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) can hydrolyze extracellular 2 ', 3 '-cGAMP and reduce extracellular 2 ', 3 '-cGAMP concentration. ENPP1 has been validated to play important roles in diabetes, cancers, and cardiovascular disease and now become a promising target for tumor immunotherapy. Several ENPP1 inhibitors under development have shown good anti-tumor effects alone or in combination with other agents in clinical and preclinical researches. In this review, the biological profiles of ENPP1 were described, and the structures and the structure-activity relationships (SAR) of the known ENPP1 inhibitors were summarized. This review also provided the prospects and challenges in the development of ENPP1 inhibitors.
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页数:13
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