化学
刺
癌症免疫疗法
免疫疗法
IC50型
免疫系统
细胞因子
先天免疫系统
小分子
干扰素基因刺激剂
药理学
体外
癌症研究
生物化学
免疫学
受体
工程类
航空航天工程
生物
作者
Su Hyun Ji,Miso Kang,Hyomin Ahn,Soo Yeon Baek,In‐Gyun Lee,Hanul Jeon,Hwan Won Chung,Dong Han,Shixuan Yang,Hyebin Lee,Ye-Seul Kim,Ji Hun Wi,JeeHee Lee,Youngsang Yoo,Sungbae Kang,Mihue Jang,Byungsun Jeon,Nam‐Jung Kim,Chiman Song,Sanghee Lee
标识
DOI:10.1021/acs.jmedchem.5c01021
摘要
A novel small-molecule ENPP1 inhibitor, compound 31 featuring a pyrrolopyrimidinone core, was identified. Compound 31 exhibited potent ENPP1 inhibition with an IC50 of 14.68 nM and effectively activated the STING pathway in cell lines. In addition, 31 promoted cytokine release, thereby enhancing innate immune response. Moreover, 31 demonstrated favorable ADMET properties. Compound 31 displayed significant antitumor efficacy in 4T1 and CT26 syngeneic mouse models without notable toxicity. These findings highlight the potential of 31 as a promising compound for cancer immunotherapy by enhancing STING-mediated immune activation and improving responses to immune checkpoint inhibitors.
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