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SC79

SKU: orb1305828

Description

SC79 is a blood-brain barrier permeable small molecule that acts as a specific AKT agonist by binding to its PH domain. It activates cytoplasmic AKT while inhibiting its membrane translocation, demonstrating neuroprotective effects in both cellular and animal models of neurological injury.

Research Area

Signal Transduction

Images & Validation

Key Properties

CAS Number305834-79-1
MW364.78
Purity>99.99% (May vary between batches)
FormulaC17H17ClN2O5
SMILESCCOC(=O)C(C#N)C1C(C(=O)OCC)=C(N)Oc2ccc(Cl)cc12
TargetAkt
SolubilityDMSO:242.5 mg/mL (664.78 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:5.5 mg/mL (15.08 mM)

Bioactivity

Target IC50
Akt:4 µg/mL
In Vivo
METHODS: To detect in vivo activity, SC79 (0.04 mg/g) was injected intraperitoneally into a C57 Black/6 mouse model of copper relaxation demyelination, and 5 min later middle cerebral artery occlusion (MCAO) was performed to construct an ischemic stroke model. RESULTS: A single dose of SC79 reduced the size of neocortical lesions by more than 35% and 40% at 24 h after MCAO and 1 week after MCAO, respectively. METHODS: To investigate the effect on liver injury, SC79 (10 mg/kg) was injected intraperitoneally into C57BL/6 mice, and d-Gal/LPS was injected 0.5 h later to induce liver injury. RESULTS: SC79 protected mice from TNF-α-mediated liver injury induced by d-Gal/LPS.
In Vitro
METHODS: Human cervical cancer cells were starved of HeLa serum for 1 h, treated with SC79 (4 µg/mL) for 30 min, and the expression levels of target proteins were detected by Western Blot. RESULTS: SC79 enhanced AKT phosphorylation, and SC79-induced AKT phosphorylation mainly occurred in the cytoplasm. METHODS: Human lung cancer cells A549 were treated with SC79 (10 µg/mL) for 24 h. The gene expression level was detected by qPCR. RESULTS: SC79 treatment up-regulated the expression of Nrf-2 (NFE2L2) gene itself as well as the downstream targets HO-1 and NQO-1.
Cell Research
HsSultan or NB4 cells (2.5 × 105) are plated in a 24-well plate in 500 μL of phenol red-free RPMI medium supplemented with 10% FBS. After incubation for 24 hours, each compound (8 μg/mL) is added and cultured for overnight (16–20 h). Fifty microliters of MTT solution (5 mg/mL in PBS) are added to each well. Following 2 hrs incubation, the purple formazan crystals are dissolved by directly adding in 500 μL of isopropanol with 0.1 M HCl to each well. After clearing the cell debris by centrifugation, the absorbance is measured at a wavelength of 570 nm.(Only for Reference)

Storage & Handling

Storagestore at low temperature,keep away from moisture | Powder: -20°C for 3 years | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

Akt, Inhibitor, inhibit, SC 79, SC79, SC-79, PKB, Protein kinase B

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Key Properties

No computed properties available.

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Protocol Information

SC79 (orb1305828)

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Step 1: Enter information below

(Recommended: An additional animal making an allowance for loss during the experiment)

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

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2 mg
$ 80.00
5 mg
$ 100.00
10 mg
$ 130.00
25 mg
$ 180.00
50 mg
$ 240.00
100 mg
$ 370.00
200 mg
$ 570.00
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