化学
小分子
锡克
蛋白激酶B
IκB激酶
PI3K/AKT/mTOR通路
NF-κB
细胞信号
药理学
信号转导
癌症研究
生物化学
酪氨酸激酶
医学
作者
Lei Zhang,Lei Shi,Shafer M. Soars,Joshua T. Kamps,Hang Yin
标识
DOI:10.1021/acs.jmedchem.7b01557
摘要
Excessive NF-κB activation contributes to the pathogenesis of numerous diseases. Small-molecule inhibitors of NF-κB signaling have significant therapeutic potential especially in treating inflammatory diseases and cancers. In this study, we performed a cell-based high-throughput screening to discover novel agents capable of inhibiting NF-κB signaling. On the basis of two hit scaffolds from the screening, we synthesized 69 derivatives to optimize the potency for inhibition of NF-κB activation, leading to successful discovery of the most potent compound Z9j with over 170-fold enhancement of inhibitory activity. Preliminary mechanistic studies revealed that Z9j inhibited NF-κB signaling via suppression of Src/Syk, PI3K/Akt, and IKK/IκB pathways. This novel compound also demonstrated antiinflammatory and anticancer activities, warranting its further development as a potential multifunctional agent to treat inflammatory diseases and cancers.
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