MDL | MFCD04094273 |
---|---|
Molecular Weight | 396.87 |
Molecular Formula | C22H21ClN2O3 |
SMILES | O=C(C1=CC=C(C2=CC=CC(Cl)=C2)O1)NC3=CC=C(CN4CCOCC4)C=C3 |
IC50: 3.2 µM (PKD1), 0.6 µM (Cellular PKD2), 0.7 µM (Cellular PKD3) [1]
CID 2011756 is an ATP-competitive PKD1 inhibitor, with an IC 50 of 3.2 µM. CID 2011756 decreases the phosphorylation of endogenous PKD1 Ser 916 in LNCaP cancer cells with an EC 50 of 10±0.7 µM. CID 2011756 also has cellular pan-PKD inhibitory effects, with IC 50 s of 0.6±0.1 µM and 0.7±0.2 µM for PKD2 and PKD3, respectively [1] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
Powder | -20°C | 3 years |
---|---|---|
4°C | 2 years | |
In solvent | -80°C | 6 months |
-20°C | 1 month |
DMSO : 20 mg/mL ( 50.39 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.5197 mL | 12.5986 mL | 25.1972 mL |
5 mM | 0.5039 mL | 2.5197 mL | 5.0394 mL |
10 mM | 0.2520 mL | 1.2599 mL | 2.5197 mL |
Add each solvent one by one: 10% DMSO >> 90% corn oil
Solubility: ≥ 2 mg/mL (5.04 mM); Clear solution