车站3
细胞凋亡
化学
小分子
SH2域
细胞
细胞生物学
癌症研究
计算生物学
信号转导
生物化学
生物
原癌基因酪氨酸蛋白激酶Src
作者
Jianyong Chen,Longchuan Bai,Denzil Bernard,Zaneta Nikolovska‐Coleska,Cindy Gomez,Jian Zhang,Yi Han,Shaomeng Wang
摘要
We report herein the structure-based design of a class of conformationally constrained, potent, cell-permeable small-molecule inhibitors to target the SH2 domain in STAT3. Compound 11 (CJ-1383) binds to STAT3 with a K(i) value of 0.95 µM, dose-dependently inhibits cellular STAT3 signaling and cancer cell growth, and induces apoptosis in the MDA-MB-468 cancer cell line with constitutively activated STAT3.
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