首页> 外国专利> INHIBITION OF SHP2/PTPN11 PROTEIN TYROSINE PHOSPHATASE BY NSC-117199 AND ANALOGS

INHIBITION OF SHP2/PTPN11 PROTEIN TYROSINE PHOSPHATASE BY NSC-117199 AND ANALOGS

机译:NSC-117199和类似物对SHP2 / PTPN11蛋白酪氨酸磷酸酶的抑制作用

摘要

Protein tyrosine phosphatase (PTP) Shp2 is a non-receptor PTP that involved in cell signaling and regulation of cell proliferation, differentiation, and migration. Shp2 mediates activation of kinases that are involved in the pathogenesis of human carcinoma. NSC-117199 was identified as a porent inhibitor of the protein tyrosine phosphatase (PTPa) Shp2. A focused library of analogs incorporating an isatin scaffold was designed and evaluated for inhibition of Shp2 and Shp1 PTP activities. Several compounds were identified that selectively inhibit Shp2 over Shp1 and PTP1B with low to sub-micromolar activity. Also disclosed are methods of inhibiting a protein tyrosine phosphatase in a cell and treating cancer through selective inhibition of Shp2.
机译:蛋白质酪氨酸磷酸酶(PTP)Shp2是一种​​非受体PTP,参与细胞信号传导和细胞增殖,分化和迁移的调控。 Shp2介导参与人类癌症发病机制的激酶的激活。 NSC-117199被鉴定为蛋白酪氨酸磷酸酶(PTPa)Shp2的有孔抑制剂。设计了结合了靛红支架的类似物的重点文库,并评估了其对Shp2和Shp1 PTP活性的抑制作用。鉴定出了几种化合物,这些化合物选择性抑制Shp2超过Shp1和PTP1B,具有低至亚微摩尔活性。还公开了抑制细胞中蛋白质酪氨酸磷酸酶和通过选择性抑制Shp2治疗癌症的方法。

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