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A-769662

Cat. No.:YN420272

  • CAS No. :844499-71-4

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    • 产品名称: A-769662
      CAS No.: 844499-71-4
      Chemical Name: 6,7-dihydro-4-hydroxy-3-(2'-hydroxy[1,1'-biphenyl]-4-yl)-6-oxo-thieno[2,3-b]pyridine-5-carbonitrile
      Synonyms:A 769662
      分子量:360.39
      分子式:C₂₀H₁₂N₂O₃S
      SMILES:N#CC1C(C2=C(NC1=O)SC=C2C3=CC=C(C4=CC=CC=C4O)C=C3)=O
      存储:Please store the product under the recommended conditions in theCertificate of Analysis.
      运输:Room temperature in continental US; may vary elsewhere.
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      Purity: 98%
    • 产品描述: A-769662 是一种有效的,可逆的AMPK激活剂,EC50值为 0.8 μM。
      IC50和靶点: [{name:"AMPK:0.8 μM (EC50)"}]
      In Vitro:
      In Vivo:
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    • Göransson, O., McBride, A., Hawley, S.A., et al.Mechanism of action of A-769662, a valuable tool for activation of AMP-activated protein kinaseJ. Biol. Chem.282(45),32549-32560(2007)

      Sanders, M.J., Ali, Z.S., Hegarty, B.D., et al.Defining the mechanism of activation of AMP-activated protein kinase by the small molecule A-769662, a member of the thienopyridone familyJ. Biol. Chem.282(45),32540-32548(2007)

      Scott, J.W., van Denderen, B.J.W., Jorgensen, S.B., et al.Thienopyridone drugs are selective activators of AMP-activated protein kinase β1-containing complexesChem. Biol.15,1220-1230(2013)

      Zhou, Y., Wang, D., Zhu, Q., et al.Inhibitory effects of A-769662, a novel activator of AMP-activated protein kinase, on 3T3-L1 adipogenesisBiol. Pharm. Bull.32(6),993-998(2009)

      Hsu, M.H., Savas, Ü., Lasker, J.M., et al.Genistein, resveratrol, and 5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside induce cytochrome P450 4F2 expression through an AMP-activated protein kinase-dependent pathwayJ. Pharmacol. Exp. Ther.337(1),125-136(2011)

      Treebak, J.T., Birk, J.B., Hansen, B.F., et al.A-769662 activates AMPK β1-containing complexes but induces glucose uptake through a PI3-kinase-dependent pathway in mouse skeletal muscleAm. J. Physiol. Cell Physiol.297,C1041-C1052(2009)

      Liu, X.m., Peyton, K.J., Shebib, A.R., et al.Activation of AMPK stimulates heme oxygenase-1 gene expression and human endothelial cell survivalAm. J. Physiol. Heart Circ. Physiol.300,H84-H93(2011)

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