首页> 外文期刊>Journal of Medicinal Chemistry >Inhibitors of Src homology-2 domain containing protein tyrosine phosphatase-2 (Shp2) based on oxindole scaffolds
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Inhibitors of Src homology-2 domain containing protein tyrosine phosphatase-2 (Shp2) based on oxindole scaffolds

机译:含吲哚骨架的蛋白酪氨酸磷酸酶-2(Shp2)的Src同源2域的抑制剂。

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摘要

Screening of the NCl diversity set of compounds has led to the identification of 5 (NSC-117199), which inhibits the protein tyrosine phosphatase (PTP) Shp2 with an IC50 of 47 mu M. A focused library 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 ShpI and PTP1B with low to submicromolar activity. A model for the binding of the active compounds is proposed.
机译:NCI多样性化合物的筛选已导致鉴定出5(NSC-117199),该产物可抑制蛋白酪氨酸磷酸酶(PTP)Shp2,IC50为47μM。设计并评估了结合了靛红支架的聚焦文库抑制Shp2和Shp1 PTP活性。鉴定出了几种化合物,这些化合物选择性抑制Shp2超过ShpI和PTP1B,具有低至亚微摩尔活性。提出了活性化合物结合的模型。

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