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CDK2-IN-51 is a pyrazolopyridine derivative and acts as a CDK2 inhibitor with an IC50 of 23.47 nM. It reduces the expression of DNA replication factors (Polα, MCM7, ORC2, and ORC4) and causes cell cycle arrest before the G1 phase. CDK2-IN-51 does not induce apoptosis and does not significantly affect CDK2 protein expression. This compound is applicable in colorectal cancer research.
| 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-51 is a pyrazolopyridine derivative and acts as a CDK2 inhibitor with an IC50 of 23.47 nM. It reduces the expression of DNA replication factors (Polα, MCM7, ORC2, and ORC4) and causes cell cycle arrest before the G1 phase. CDK2-IN-51 does not induce apoptosis and does not significantly affect CDK2 protein expression. This compound is applicable in colorectal cancer research. |
| Targets&IC50 | CDK2:23.47 nM |
| In vitro | CDK2-IN-51 (compound 6) at concentrations of 10-50 μM for 24-72 hours exhibits significant antiproliferative activity in HCT-116 and HT-29 cells, while showing no cytotoxic effects on NCM-460D cells. At concentrations of 40-50 μM for 48 hours, it induces G1 phase pre-stage arrest in HCT-116 and HT-29 cells without causing S phase arrest. Additionally, at these concentrations and duration, CDK2-IN-51 downregulates CDK2 protein targets involved in DNA replication, such as Polα, MCM7, ORC2, and ORC4, without promoting apoptosis or significantly affecting the expression of CDK2 protein. |
| Molecular Weight | 288.35 |
| Formula | C18H16N4 |
| Cas No. | 1443-10-3 |
| Smiles | N=1C2=NN3C(N=C(C=C3C)C)=C2C(=CC1C)C=4C=CC=CC4 |
| 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.
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