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TLR7型
药效学
计算生物学
药理学
小分子
医学
体内
免疫疗法
免疫检查点
癌症免疫疗法
药代动力学
药物发现
癌症
癌症研究
免疫系统
化学
生物信息学
Toll样受体
内科学
生物
免疫学
生物化学
先天免疫系统
生物技术
作者
Liqi He,Meng Yao Zhang,Matthew Cox,Qian Zhang,Andrew F. Donnell,Yong Zhang,Christine M. Tarby,Patrice Gill,Murugaiah A. M. Subbaiah,Thangeswaran Ramar,Maheswara Reddy,Vijaya Puttapaka,Yixin Li,Prasanna Sivaprakasam,David Critton,Dawn Mulligan,Chunshan Xie,Radha Ramakrishnan,Jignesh Nagar,Shailesh Dudhgaonkar
标识
DOI:10.1021/acsmedchemlett.3c00456
摘要
Small molecule toll-like receptor (TLR) 7 agonists have gathered considerable interest as promising therapeutic agents for applications in cancer immunotherapy. Herein, we describe the development and optimization of a series of novel TLR7 agonists through systematic structure–activity relationship studies focusing on modification of the phenylpiperidine side chain. Additional refinement of ADME properties culminated in the discovery of compound 14, which displayed nanomolar reporter assay activity and favorable drug-like properties. Compound 14 demonstrated excellent in vivo pharmacokinetic/pharmacodynamic profiles and synergistic antitumor activity when administered in combination with aPD1 antibody, suggesting opportunities of employing 14 in immuno-oncology therapies with immune checkpoint blockade agents.
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