MDL | MFCD26960956 |
---|---|
Molecular Weight | 276.25 |
Molecular Formula | C16H8N2O3 |
SMILES | O=C1C2=C(OC(C3=CC=CN=C3)=N2)C(C4=CC=CC=C41)=O |
SJB3-019A is a potent and novel USP1 inhibitor, 5 times more potent than SJB2-043 in promoting ID1 degradation and cytoxicity in K562 cells with IC 50 of 0.0781 μM.
IC50: 78.1 nM (ID1)
SJB3-019A (IC 50 =0.0781 μM) is 5 times more potent than SJB2-043 in promoting ID1 degradation and cytoxicity in K562 cells. SJB3-019A increases the levels of Ub-FANCD2 and Ub-PCNA, and decreases the HR activity [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 ( 36.20 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 3.6199 mL | 18.0995 mL | 36.1991 mL |
5 mM | 0.7240 mL | 3.6199 mL | 7.2398 mL |
10 mM | 0.3620 mL | 1.8100 mL | 3.6199 mL |
Add each solvent one by one: 10% DMSO >> 90% corn oil
Solubility: ≥ 1 mg/mL (3.62 mM); Clear solution