GF109203X

CAT:
400-SIH-447-10MG
Size:
10 mg
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
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GF109203X

  • Background :

    GF109203X is a very potent inhibitor of protein kinase C; it is selective for the α and β1 isoforms; this could lead to an increase in autophagy. GF109203X is also an inhibitor of glycogen synthase kinase-3 (GSK-3) and has anti-inflammatory effects. It has also been seen to inhibit telomerase activity and necrosis.
  • Description :

    PKC kinase inhibitor
  • Product Name Alternative :

    2-[1- (3-Dimethylaminopropyl) indol-3-yl]-3- (indol-3-yl) maleimide, 3- (N-[Dimethylamino]propyl-3-indolyl) -4- (3-indolyl) maleimide, 3-[1-[3- (Dimethylamino) propyl]1H-indol-3-yl]-4- (1Hindol-3-yl) 1H-pyrrole-2,5dione, Bisindolylmaleimide I
  • UNSPSC :

    41116105
  • Type :

    Inhibitor
  • Source :

    Synthetic
  • Field of Research :

    Cell Signaling | Cancer | Apoptosis | Cancer Growth Inhibitors | Tyrosine Kinase Inhibitors
  • Purity :

    ≥98% (TLC)
  • Weight :

    0.01
  • Format :

    Red solid
  • Solubility :

    Soluble in dimethyl formamide or DMSO (10 mg/ml, warm to 40°C and vortex well)
  • Molecular Formula :

    C25H24N4O2
  • Molecular Weight :

    412.5
  • Precautions :

    Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
  • References & Citations :

    1. Toullec D., et al. (1991) J. Biol. Chem. 266(24): 15771–15781. 2. Jacobson P.B., et al. (1995) J. Pharma. Exp. Ther. 275(2): 995–1002. 3. Jiang Q., et al. (2011) Mol. Biol. Cell. 22(8): 1167–1180. 4. Kuchera S., et al. (1993) Agents and Actions. 39 Spec No: C169–173.
  • CAS Number :

    133052-90-1

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