申请人:McMurray S. John
公开号:US20070010428A1
公开(公告)日:2007-01-11
Stat3 inhibitor compounds are disclosed, wherein the compounds are structural analogs of Ac-pTyr-Leu-Pro-Gln-Thr-NH
2
and bind to the SH2 domain of Stat3 under physiological conditions to inhibit a cellular signaling activity of Stat3.
抑制剂化合物Stat3被披露,其中这些化合物是Ac-pTyr-Leu-Pro-Gln-Thr-NH2的结构类似物,并在生理条件下与Stat3的SH2结构域结合,从而抑制Stat3的细胞信号活性。