虚拟筛选
化学
药物发现
车站3
激酶
STAT蛋白
转录因子
小分子
信号转导
细胞生物学
STAT1
高通量筛选
激活剂(遗传学)
对接(动物)
磷酸化
抄写(语言学)
生物信息学
斯达
生物化学
JAK-STAT信号通路
生物
受体
基因
作者
Mingming Zhang,Weiliang Zhu,Ning Ding,Wei Zhang,Yingxia Li
标识
DOI:10.1016/j.bmcl.2013.01.056
摘要
Inhibition of the signal transducer and activator of transcription 3 (STAT3) signaling pathway has been considered a novel therapeutic strategy to treat human cancers that harbor aberrantly-active STAT3. In this study, a series of small molecules were identified as novel inhibitors of STAT3 signaling pathway through virtual screening. A tricyclic scaffold containing compound, 6, was identified as an inhibitor of IL-6/STAT3 signaling with an IC50 of 26.68 μM. In addition, this compound inhibited Tyr705 phosphorylation of STAT3 and had no obvious effect on upstream tyrosine kinases. Thus, compound 6 is a potential lead structure and valuable for further drug development.
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