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Potent Chk2 inhibitor (IC50 = 3 nM). Shows >63-fold selectivity for Chk1 over Chk2 and a panel of 84 other kinases. Inhibits Chk2 activation in response to etoposide-induced DNA damage in HT29 cells. Blocks ionizing radiation-induced apoptosis of mouse thymocytes.

| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 10 mg | $1,420 | 35 days |
| Description | Potent Chk2 inhibitor (IC50 = 3 nM). Shows >63-fold selectivity for Chk1 over Chk2 and a panel of 84 other kinases. Inhibits Chk2 activation in response to etoposide-induced DNA damage in HT29 cells. Blocks ionizing radiation-induced apoptosis of mouse thymocytes. |
| Targets&IC50 | Chk1:245 nM (IC50), Chk2:1.16 nM (Ki), Chk2:3 nM (IC50) |
| Synonyms | CCT 241533 dihydrochloride |
| Molecular Weight | 515.41 |
| Formula | C23H29Cl2FN4O4 |
| Cas No. | 1962925-28-5 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |
| Solubility Information | DMSO: Soluble |

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