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A-769662

SKU: orb1305442

Description

A-769662

Research Area

Epigenetics & Chromatin, Metabolism Research, Signal Transduction

Images & Validation

Key Properties

CAS Number844499-71-4
MW360.39
Purity98.72%
FormulaC20H12N2O3S
SMILESOc1ccccc1-c1ccc(cc1)-c1csc2[nH]c(=O)c(C#N)c(O)c12
TargetFatty Acid Synthase,AMPK
SolubilityDMSO:51 mg/mL (141.51 mM);10% DMSO+40% PEG300+5% Tween 80+45% Saline:4.5 mg/mL (12.49 mM);Ethanol:3.61 mg/mL (10.02 mM)

Bioactivity

Target IC50
AMPK:0.8 μM(EC50)
In Vivo
A-769662 activates AMPK, purified from various tissues and species, in a dose-dependent manner, demonstrated across purified rat liver (EC5 = .8 μM), rat heart (EC5 = .2 mM , rat musclee (EC5 = .9 mM), and human embryonic kidney cells (HEKs) (EC5 = .1 mM . In hepatocytes, A-769662 enhances ACC phosphorylation and inhibits fatty acid synthesis, with IC50 Values of 3.2 μM in Primary rat hepatocytes and 3.6 μM in mouse hepatocytes the activation of AMPK by A-769662 involves preventin the dephosphorylation at Thr-172 and structural modulation. furthermore , A-769662 inhibit the in vitro activity o the purified 26S proteasome, as well as cell proliferation and DNA synthesis.
In Vitro
In ob/ob mice, A-769662 (30 mg/kg, b.i.d.) effectively reduce the hepatic expression of PEPCK, G6Pase, and FAS, decreases plasma glucose levels, and lowers triglyceride levels In both plasma and liver, thereby mitigating weight gain.
Cell Research
Cell viability of MEF cells treated or not with A-769662 is performed as follows: cells are Harvested by trypsinization and incubated with 0.5 mg mL RNase and 50 μg mL propidium iodine at room temperature in the dark; cell viability is analyzed by flow cytometry using a FACScanto flow cytometer, using an excitation laser at 488 nM and a propidium iodine fluorescence detection at 600 nM. To determin the proportion of cells in Each phase o the cell cycle, cells are Harvested by trypsinization, collected by centrifugation, washed in PBS and fixed overnight in 80% ethanol at -20 °C. Subsequently, these fixed cells are centrifuged to remov the fixative and incubated for 20 minutes in the dark at room temperature in PBS containing 0.5 mg mL RNase and 50 μg mL propidium iodine. Flow cytometry analysis is performed as above the proportion of cells in G1, S, and G2 is determined usin the MODFIT program. Cell culture pictures are taken a the indicated times using a camera coupled to an inverted microscope with a 20 × objective. (Only for Reference)

Storage & Handling

StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature.
Expiration Date12 months from date of receipt.
DisclaimerFor research use only

Alternative Names

AMP-activated protein kinase, AMPK, A769662, A-769662, A 769662, FAS, Fatty Acid Synthase, FattyAcidSynthase, inhibit, Inhibitor

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    844499-71-4

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    C20H12N2O3S

    1 g, 500 mg, 100 mg, 50 mg, 2 mg, 5 mg, 10 mg, 25 mg
Quality Guarantee

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Key Properties

No computed properties available.

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A-769662 (orb1305442)

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Step 1: Enter information below

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

Step 2: Enter the in vivo formulation

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% DMSO +
%+
% Tween 80 +
%

Available Sizes

Select a size below

2 mg
$ 80.00
1 ml x 10 mM (in DMSO)
$ 100.00
5 mg
$ 100.00
10 mg
$ 120.00
25 mg
$ 190.00
50 mg
$ 310.00
100 mg
$ 530.00
500 mg
$ 1,110.00
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