A-769662 (CAS: 844499-71-4)
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SKU-Pack Size | Availability | Size | Price | |
EBC51011-1ML | In Stock | 1mL(10mM in DMSO) | ¥690.00 | |
EBC51011-2MG | In Stock | 5mg | ¥590.00 | |
EBC51011-10MG | In Stock | 10mg | ¥790.00 | |
EBC51011-25MG | In Stock | 25mg | ¥1390.00 | |
EBC51011-50MG | In Stock | 50mg | ¥2490.00 |
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北京美瑞克生物科技有限公司 | Phone: +86 010-62890160 / 13691184142(微信同号) | |
2 / F, 128 malianwa North Road, Haidian District, | E-mail: mrkbio@163.com | |
China | Beijing China | Website: www.mrkbio.com |
Product Information | |||||||||||||||||||||
Synonym(s) | A769662, A 769662 | ||||||||||||||||||||
Chemical Name | 6,7-dihydro-4-hydroxy-3-(2′-hydroxy[1,1′-biphenyl]-4-yl)-6-oxo-thieno[2,3-b]pyridine-5-carbonitrile | ||||||||||||||||||||
Application | A-769662 is an AMPK activator which induces PI3-kinase-dependent glucose uptake and inhibits AMPK dephosphorylation. | ||||||||||||||||||||
CAS Number | 844499-71-4 | ||||||||||||||||||||
Purity | ≥99.0% | ||||||||||||||||||||
Molecular Weight | 360.39 | ||||||||||||||||||||
Molecular Formula | C₂₀H₁₂N₂O₃S | ||||||||||||||||||||
SMILES | C1=CC=C(C(=C1)C2=CC=C(C=C2)C3=CSC4=C3C(=C(C(=O)N4)C#N)O)O | ||||||||||||||||||||
Target & IC50 | AMPK EC50= 0.8 μM | ||||||||||||||||||||
Solubility | DMSO: 36 mg/mL (100 mM) Ethanol: 3.6 mg/mL (10 mM) |
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Preparing Stock Solutions |
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Shipping | Gel Pack | ||||||||||||||||||||
Storage | Store at 4° C | ||||||||||||||||||||
Research Use | For Research Use Only. Not Intended for Diagnostic Or Therapeutic Use. |
Product Description | |
A-769662 is an AMP-activated protein kinase (AMPK) activator that mimics the function of AMP on AMPK β-1 by allosteric activation and the inhibition of dephosphorylation of AMPK. In the prescence of both LKB1 and A-769662, the phosphorylation of AMPK is suppressed. In addition, A-769662 is not effected by upstream kinases such as calmodulin-dependent protein kinase kinase-β when phosphorylating AMPK beta-1. In vitro tests indicate A-769662 suppresses the activity of Sodium-Potassium Adenosine Triphosphatase by inhibiting the α(1)-isoform of the pump and decreasing the cell surface abundance of the protein complex in skeletal muscle cells and induces glucose uptake through a PI3-kinase-dependent pathway. |
Specific Protocols | |