MDL | MFCD02683960 |
---|---|
Molecular Weight | 349.29 |
Molecular Formula | C16H17BrN2S |
SMILES | CC1=CC=C(C2=CN3C(SC4=C3CCCC4)=N2)C=C1.Br |
Pifithrin-β hydrobromide (PFT β hydrobromide) is a potent p53 inhibitor with an IC 50 of 23 μM.
IC50: 23 μM (p53) [1]
Pifithrin-α hydrobromide (PFT β hydrobromide), an inhibitor of the p53 protein, is regarded as a lead compound for cancer and neurodegenerative disease therapy. Pifithrin-α is very unstable in culture medium and rapidly converts to its condensation product pifithrin-β, the N-acetyl derivative [2] . After 24 h, the viability assay shows that the pretreatments with 1 and 10 μM pifithrin-β exerts neuroprotective effects [3] .
MCE has not independently confirmed the accuracy of these methods. They are for reference only.
Solid
Room temperature in continental US; may vary elsewhere.
4°C, sealed storage, away from moisture
* In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)
DMSO : 10 mg/mL ( 28.63 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 2.8630 mL | 14.3148 mL | 28.6295 mL |
5 mM | 0.5726 mL | 2.8630 mL | 5.7259 mL |
10 mM | 0.2863 mL | 1.4315 mL | 2.8630 mL |