Potent, cell permeable, selective ATP-competitive inhibitor of CDK1/cyclin B (IC50=700nM), CDK5/p25 (IC50=1.5µM), and GSK-3 (IC50=920nM).
Product Specification
| Alternative Name: | RP106, 7-n-Butyl-6-(4-methoxyphenyl)[5H]pyrrolo[2,3-b]pyrazine |
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| Identity: | Identity determined by NMR. |
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| Formula: | C17H19N3O |
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| MW: | 281.4 |
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| Purity: | ≥95% (HPLC) |
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| Appearance: | Off-white solid. |
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| CAS: | 496864-15-4 |
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| Solubility: | Soluble in DMSO (200mg/ml) or methanol (200mg/ml). |
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| Long Term Storage: | +4°C |
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| Handling: | Packaged under inert gas. Protect from light. |
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Product Literature References
Aloisines, a new family of CDK/GSK-3 inhibitors. SAR study, crystal structure in complex with CDK2, enzyme selectivity, and cellular effects: Y. Mettey, et al.; J. Med. Chem.
46, 222 (2003),
Abstract;