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CDK7-IN-27 (Compound 37) is a selective inhibitor of cyclin-dependent kinase 7 (CDK7), with a Ki value of 3 nM. It effectively causes cell cycle arrest at the G0/G1 phase.

| Description | CDK7-IN-27 (Compound 37) is a selective inhibitor of cyclin-dependent kinase 7 (CDK7), with a Ki value of 3 nM. It effectively causes cell cycle arrest at the G0/G1 phase. |
| Targets&IC50 | CDK7:3 nM, CDK2:19.4 nM |
| In vitro | CDK7-IN-27 effectively inhibits the proliferation of MDA-MB-453 cells with an EC50 of 1.49 μM when used in concentrations ranging from 0.04 to 10 μM over the course of 5 days. At a concentration of 1 μM over 24 hours, CDK7-IN-27 demonstrates good metabolic stability in both mouse and human liver microsomes, with half-life periods of 38.5 minutes and 34.1 minutes, respectively. Additionally, CDK7-IN-27 (0-1 μM, 24 h) arrests the cell cycle in the G0/G1 phase by inhibiting the phosphorylation of retinoblastoma protein through CDK7 inhibition. |
| Formula | C26H37N7O2 |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. |

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