AS 1938909是一种有效的SHIP 2抑制剂(Ki = 0.44uM)。该化合物对一些相关的磷酸酶显示出显著的选择性(对mSHIP 2、hSHIP 2、hPTEN的IC 50分别为0.18 μ M、21 μ M、50 μ M)。参考文献A Suwa T Yamanoto et al.“Glucose metabolism activation by SHIP2 inhibitors via up-regulation of GLUT1 gene in L6 myotubes”Eur J Pharmaco 2010 642 177
产品描述
AS1938909 is a potent SHIP2 inhibitor (Ki = 0.44uM). This compound shows signficant selectivity over some related phosphatases (IC50 = 0.18uM 21uM >50uM for mSHIP2 hSHIP2 hPTEN respectively). It also enhances Akt phosphorylation and increases glucose consumption and uptake in L6 myotubes.ReferencesA Suwa T Yamanoto et al. "Glucose metabolism activation by SHIP2 inhibitors via up-regulation of GLUT1 gene in L6 myotubes" Eur J Pharmaco 2010 642 177