產(chǎn)品詳情
簡單介紹:
MK-2206
詳情介紹:
Characteristics | A highly selective non-ATP competitive allosteric Akt inhibitor with IC50,'s of 8 nM, 2 nM and 65 nM for Akt1, Akt2 and Akt3, respectively. MK-2206 potently inhibits phosphorylation of Thr308 and Ser473 in 3T3-L1 adipocytes with IC50 values of 0.11 and 0.18 μM, respectively as well as downstream effects of insulin on GLUT4 translocation (IC50 = 0.47 μM) and glucose transport (IC50 = 0.14 μM). In addition, treatment with MK-2206 causes a robust, concentration-dependent activation of autophagy in human glioma cell lines LN229 and T98G. |
Purity | ≥ 98?% by HPLC |
Chemical Name | 8-(4-(1-Aminocyclobutyl)phenyl-9-phenyl[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3(2H)-one dihydrochloride |
Formula | C??H??N?O .2HCl |
Permeability | Cell-permeable |
Molecular Weight | 480.39 g/mol |
CAS-No | 1032350-13-2 |
Research Area | Kinases/Phosphatases |
Restrictions | For Research Use only |
Format | Solid |
Handling Advice | Protect from air and moisture |
Storage | -20 °C |
Expiry Date | 36 months |
Supplier Images |
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Product cited in: |
Cheng, Whitsett, Tran, Winkles: "The TWEAK Receptor Fn14 is a Src-inducible Protein and a Positive Regulator of Src-driven Cell Invasion." in: Molecular cancer research : MCR, 2014 (PubMed).
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