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Inhibitor Libraries
  GSK-3 Inhibitor XV
Cat. No. 361558  
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Glycogen Synthase Kinase (GSK)

Purple solid. PROTECT FROM LIGHT. PACKAGED UNDER INERT GAS. The racemic mixture of a cell-permeable pyridocarbazolo-cyclopentadienyl Ruthenium complex that acts as a reversible, ATP-competitive, and highly potent inhibitor of GSK-3 (IC50 = 0.4 and 0.6 nM for GSK-3a and GSK-3b, respectively) with ∼5-fold selectivity over PIM-1 kinase (IC50 = 3 nM). Studies using isolated enantiomers have shown that the (R)-enantiomer is GSK-3-selective (IC50 = 0.35, 0.55, and 35 nM for GSK-3a GSK-3b, and Pim-1, respectively) and interferes with normal zebrafish embryo development (1 µM), while the (S)-enantiomer is Pim-1-selective (IC50 = 80, 90, and 3 nM for GSK-3a GSK-3b, and Pim-1, respectively) and exhibits no effect in embryo development at the same dosage. Purity: ≥98% by HPLC.

Ref.: Atilla-Gokcumen, G.E., et al. 2006. ChemBioChem 7, 1443.
Sold for research purposes only, pursuant to an agreement with University of Pennsylvania.

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1 mgY$262.00


SolubilityMolecular FormulaMol. Wt.
DMSO C25H14BrN3O6Ru 633.4 


Material Safety Data Sheets:
361558: GSK-3 Inhibitor XV - English

Related Categories:
All Categories » Calbiochem » Inhibitors » Kinase and Phosphatase » Glycogen Synthase Kinase (GSK)