| MDL | MFCD28167759 |
|---|---|
| Molecular Weight | 275.26 |
| Molecular Formula | C15H9N5O |
| SMILES | N#CC1=C(C#N)N=C2C(/C(C3=C2C=CC=C3)=N/OCC)=N1 |
DUB-IN-2 is a potent deubiquitinase inhibitor with an IC 50 of 0.28 μM for USP8 [1] .
IC50: 0.28 μM (USP8) [1]
DUBs-IN-2 (compound 22 e) is a potent USP8 inhibitor with an IC 50 of 0.28 μM, and has no effect on USP7, with an IC 50 of >100 μM. DUBs-IN-2 inhibits the viability of HCT116 colon cell line and PC-3 prostate cancer cell line with IC 50 values of 0.5-1.5 μM [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 : 10 mg/mL ( 36.33 mM ; Need ultrasonic)
| Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
|---|
| 1 mM | 3.6329 mL | 18.1646 mL | 36.3293 mL |
| 5 mM | 0.7266 mL | 3.6329 mL | 7.2659 mL |
| 10 mM | 0.3633 mL | 1.8165 mL | 3.6329 mL |
Add each solvent one by one: 50% PEG300 >> 50% saline
Solubility: 1.5 mg/mL (5.45 mM); Suspended solution; Need ultrasonic