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| Product Name | Akt Inhibitor, Isozyme-selective |
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| Description | Purity ~97% (HPLC). Cell-permeable. A potent and selective inhibitor of Akt1/Akt2 activity (IC50 = 58nM (Akt1), 210nM (Akt2) and 2.12uM (Akt3) in in vitro kinase assays). The inhibition appears to be pleckstrin homology (PH) domain-dependent. It does not exhibit any inhibitory effect against PH domain-lacking Akts, or other closely related AGC family kinases, PKA, PKC, and SGK, even at concentrations (50uM). Solubility: DMSO Molecular Weight: ~551.65 |
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| Size | 1mg |
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| Concentration | n/a |
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| Applications | n/a |
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| Other Names | Akt Inhibitor, Isozyme-selective (1,3-Dihydro-1-(1-((4-(6-phenyl-1H-imidazo[4,5-g]quinoxalin-7-yl)phenyl)methyl)-4-piperidinyl)-2H-benzimidazol-2-one; Akti-1/2) |
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| Gene, Accession, CAS # | n/a |
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| Catalog # | A1124-20B |
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| Price | |
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| Order / More Info | Akt Inhibitor, Isozyme-selective from UNITED STATES BIOLOGICAL |
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| Product Specific References | n/a |
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