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Synonyms:
CDK2-IN-56
| Pack Size | Price | USA Stock | Global Stock | Quantity |
|---|---|---|---|---|
| 10 mg | Inquiry | 10-14 weeks | 10-14 weeks | |
| 50 mg | Inquiry | 10-14 weeks | 10-14 weeks |
| Description | CDK2-IN-56 (compound 39) is a pyrazolo[3,4-b]quinazoline-3-carboxamide compound that acts as a CDK2/CyA inhibitor, and it is applicable in cancer research. |
| In vitro | CDK2-IN-56 (Cpd39) is a potent inhibitor of CDK2/CyA, with an experimental pIC50 value of 8.699. Its activity can be accurately predicted using CoMFA and CoMSIA 3D-QSAR models. |
| Molecular Weight | 419.50 |
| Formula | C18H25N7O3S |
| Cas No. | 802536-13-6 |
| Smiles | O=C(NC)C1=NN(C=2C=3N=C(N=CC3CCC12)NC4CCN(CC4)S(=O)(=O)C)C |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 µL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 µL Tween 80 and mix well until fully clarified.
3) Add 450 µL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
| Size | Quantity | Unit Price | Amount | Operation |
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