

ab120421 · 1 mg
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Description
MW 721.8 Da, Purity >98 %. Cell-permeable, reversible and selective inhibitor of CaM kinase II IC50 = 500 nM . Interacts with the calmodulin binding site of the enzyme. At higher concentrations reported to inhibit GSK3beta, PRAK and MAPKAP-K2. Also potent non-competitive antagonist at the P2X7 receptor IC50 = 15 nM .






