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Description
Selective, cell-permeable inhibitor of CaM kinase II (IC50 = 0.9 μM). Binds directly to the calmodulin binding site of the enzyme. Potent non-competitive antagonist at the P2X7 receptor (IC50 = 15 nM).
Specifications
Specifications
| Quantity | 1 mg |
| Formula Weight | 721.84 |
| Purity | >98% |
| Molecular Weight (g/mol) | 721.85 |
| Chemical Name or Material | KN-62 |
Safety and Handling
| Recommended Storage | Desiccate at -20°C |
Product Title
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