Name | Cdk1 Inhibitor |
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Synonyms |
2H-Indol-2-one, 3-[(2-chloro-1H-indol-3-yl)methylene]-1,3-dihydro-, (3E)-
(3E)-3-[(2-Chloro-1H-indol-3-yl)methylene]-1,3-dihydro-2H-indol-2-one (3E)-3-[(2-chloro-1H-indol-3-yl)methylidene]-1,3-dihydro-2H-indol-2-one Cdk1 Inhibitor |
Description | CDK1-IN-2 is a CDK1 inhibitor (IC50: 5.8 μM)[1]. |
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Related Catalog | |
Target |
CDK1:5.8 μM (IC50) |
In Vitro | CDK1-IN-2 (“CDK1 inhibitor 1”, 0-19.8 μM, 24 h) arrests HCT-116 cells in G2/M phase[1]. |
Density | 1.5±0.1 g/cm3 |
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Boiling Point | 585.1±50.0 °C at 760 mmHg |
Molecular Formula | C17H11ClN2O |
Molecular Weight | 294.735 |
Flash Point | 307.7±30.1 °C |
Exact Mass | 294.056000 |
LogP | 4.02 |
Vapour Pressure | 0.0±1.6 mmHg at 25°C |
Index of Refraction | 1.778 |
Storage condition | 2-8°C |