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How to Cite 1. For In-Text Citation (Materials & Methods): 2. For Key Resources Table: |
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| Formula | C17H17ClN2O5 |
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| Molecular Weight | 364.78 | CAS No. | 305834-79-1 | ||||
| Solubility (25°C)* | In vitro | DMSO | 72 mg/mL (197.37 mM) | ||||
| Ethanol | 72 mg/mL (197.37 mM) | ||||||
| Water | Insoluble | ||||||
| In vivo (Add solvents to the product individually and in order) |
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* <1 mg/ml means slightly soluble or insoluble. * Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations. * Room temperature shipping (Stability testing shows this product can be shipped without any cooling measures.) |
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| Description | SC79 is a brain-penetrable Akt phosphorylation activator and an inhibitor of Akt-PH domain translocation. | |
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| In vitro | SC79 suppresses PHAKTM-GFP plasma membrane translocation, and enhances phosphorylation of all three Akt isoforms in HEK293, HeLa, HL60, NB4, and HsSulton (B cells) cells. This compound reduces neuronal excitotoxicity and prevents stroke-induced neuronal death. It restores proliferation of BRAT1 knockdown cells, and reduces the production of superoxide in mitochondria of MitoSox positive cells. |
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| In vivo | In the permanent focal cerebral ischemia mouse model, SC79 (0.04 mg/g, i.p.) enables the cytosolic activation of Akt, and recapitulates the primary cellular function of Akt signaling, resulting in augmented neuronal survival. |
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Data from [ , , J Exp Clin Cancer Res, 2018, 37(1):41 ]

Data from [ , , J Exp Clin Cancer Res, 2017, 36(1):105 ]

Data from [ , , EBioMedicine, 2018, 34:35-45 ]

Data from [ , , Biochim Biophys Acta Mol Basis Dis, 2017, 1863(11):2848-2861 ]
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