Molecular Formula | C18H19ClN4O2 |
Molar Mass | 358.82 |
Density | 1.39±0.1 g/cm3(Predicted) |
Melting Point | 170-172°C |
Boling Point | 647.5±55.0 °C(Predicted) |
Solubility | Chloroform, methanol |
Appearance | Solid |
Color | Off-White to Pale Yellow |
pKa | 14.43±0.10(Predicted) |
Storage Condition | -20°C Freezer |
In vitro study | CMK inhibits the growth of Cdc5 (L158G) with IC 50 of 36 nM, greater than 30 μM for wild type Cdc5. CMK exhibits a concentration-dependent first cell cycle mitotic arrest in the cdc5-as1 strain with an IC 50 of 1.1 μM. CMK inhibition of Cdc5 (L158G) leads to a first cell cycle anaphase arrest and delay in anaphase spindle migration. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.787 ml | 13.934 ml | 27.868 ml |
5 mM | 0.557 ml | 2.787 ml | 5.574 ml |
10 mM | 0.279 ml | 1.393 ml | 2.787 ml |
5 mM | 0.056 ml | 0.279 ml | 0.557 ml |
biological activity | cmks are RSK2 kinase inhibitors with similar potency but lower chemical stability than fmks. |