化学
硝基呋喃
小分子
药品
刺
先天免疫系统
组合化学
药理学
生物化学
受体
医学
遗传学
生物
工程类
航空航天工程
作者
Liang Xue,Ruixue Liu,Lican Zhang,Tingting Qiu,Lu Liu,Ruijuan Yin,Tao Jiang
标识
DOI:10.1016/j.ejmech.2024.116883
摘要
Aberrant activation of the innate immune molecule STING can initiate inflammation and autoimmune diseases. Small molecule inhibitors targeting STING have demonstrated therapeutic efficacy against these conditions. Moreover, employing degradants to target STING represents a novel approach to drug design strategy. Consequently, we have designed and synthesized a series of covalent degradants targeting STING. Among them, compound P8 exhibited the highest degradation capacity, with a 24-h DC
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