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ex229 (compound 991) AMPK activator

Cat.No.S8654

EX229 (compound 991) is a potent AMPK activator that is 5-10-fold more potent than A769662 in activating AMPK.
ex229 (compound 991) AMPK activator Chemical Structure

Chemical Structure

Molecular Weight: 431.87

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Quality Control

Batch: S865401 DMSO]12 mg/mL]false]Water]Insoluble]false]Ethanol]Insoluble]false Purity: 98.83%
  • Cited in Nature Medicine for its top-tier quality
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98.83

Cell Culture, Treatment & Working Concentration

Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
Sf21 Function assay 30 mins Agonist activity at human recombinant phosphorylated AMPK complex 7 alpha2/beta1/gamma1 expressed in baculovirus infected Sf21 cells assessed as phosphorylation of 5-FAM-labeled SAMS substrate preincubated for 30 mins in presence of AMPK activator followe, EC50=0.002μM 29035567
Sf21 Function assay 30 mins Activation of full length human recombinant AMPK alpha1/beta1/gamma1 expressed in baculovirus infected sf21 cells using SAMS peptide substrate after 30 mins in presence of [33P]ATP by TopCount analysis, EC50=0.003μM 27727125
Click to View More Cell Line Experimental Data

Solubility

In vitro
Batch:

DMSO : 12 mg/mL (27.78 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

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Mass Concentration Volume Molecular Weight
Dilution Calculator Molecular Weight Calculator

In vivo
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In vivo Formulation Calculator (Clear solution)

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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Chemical Information, Storage & Stability

Molecular Weight 431.87 Formula

C24H18ClN3O3

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 1219739-36-2 -- Storage of Stock Solutions

Synonyms N/A Smiles CC1=C(C=C(C=C1)OC2=NC3=C(N2)C=C(C(=C3)C4=CC5=C(C=C4)N(C=C5)C)Cl)C(=O)O

Mechanism of Action

Targets/IC50/Ki
AMPK
In vitro

EX229 (compound 991) activates AMPK in incubated rat epitrochlearis skeletal muscle and increases glucose uptake upon incubation with rat skeletal muscle. The stimulation of skeletal muscle glucose uptake by this compound is PI3K/PKB-independent, while AMPK-dependent. It also increases fatty acid oxidation and glucose uptake in L6 myotubes.

References

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