TLR7型
Toll样受体
药理学
药效学
干扰素
受体
肿瘤坏死因子α
体内
化学
TLR3型
药代动力学
病毒学
免疫学
医学
生物化学
生物
先天免疫系统
生物技术
作者
Paul A. Roethle,Ryan M. L. McFadden,Hong Zhen Yang,Paul Hrvatin,Hon Hui,Michael Graupe,Brian B. Gallagher,Jessica Chao,Joseph Hesselgesser,Paul Duatschek,Jim Zheng,Bing Lu,Daniel B. Tumas,Jason K. Perry,Randall L. Halcomb
摘要
Pteridinone-based Toll-like receptor 7 (TLR7) agonists were identified as potent and selective alternatives to the previously reported adenine-based agonists, leading to the discovery of GS-9620. Analogues were optimized for the immunomodulatory activity and selectivity versus other TLRs, based on differential induction of key cytokines including interferon α (IFN-α) and tumor necrosis factor α (TNF-α). In addition, physicochemical properties were adjusted to achieve desirable in vivo pharmacokinetic and pharmacodynamic properties. GS-9620 is currently in clinical evaluation for the treatment of chronic hepatitis B (HBV) infection.
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