Powder: -20°C for 3 years | In solvent: -80°C for 1 year
AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes[1][2]. AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor, with an IC50 of 620 nM.
説明 | AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes[1][2]. AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor, with an IC50 of 620 nM. |
ターゲット&IC50 | SHIP2:620 nM |
分子量 | 371.88 |
分子式 | C20H18ClNO2S |
CAS No. | 1203680-76-5 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
DMSO: 49 mg/mL (131.76 mM)
You can also refer to dose conversion for different animals. 詳細
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AS1949490 1203680-76-5 Metabolism Phosphatase inhibit Protein kinase B glucose uptake diabetes insulin signalling pathway AS 1949490 Akt glucose consumption Inhibitor PKB L6 myotubes AS-1949490 inhibitor