MDL | MFCD00238878 |
---|---|
Molecular Weight | 296.34 |
Molecular Formula | C13H14F2N4S |
SMILES | S=C(NCCCN1C=CN=C1)NC2=CC=C(F)C=C2F |
IR415 is a potent anti-HBV agent and inhibits HBV replication by blocking the HBx activity. IR415 selectively interacts with HBx ( K d =2 nM) and blocks HBV-mediated RNAi suppression, reverses the inhibitory effect of HBx protein on the activity of the dicer endoribonuclease [1] . HBx: hepatitis B virus X protein.
Kd: 2 nM (IR415-HBx interaction) [1]
Hepatitis B virus X protein (HBx) as a suppressor of host defenses consisting of RNAi-based silencing of viral genes
[1]
.
IR415 (50-200 μM) has a dose-dependent inhibitory effect on HBx, with a minimal effective concentration of 50 μM in HepG2/GFP-shRNA line transfected with HBx
[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 : 125 mg/mL ( 421.81 mM ; Need ultrasonic)
Concentration Solvent Mass | 1 mg | 5 mg | 10 mg |
---|
1 mM | 3.3745 mL | 16.8725 mL | 33.7450 mL |
5 mM | 0.6749 mL | 3.3745 mL | 6.7490 mL |
10 mM | 0.3375 mL | 1.6873 mL | 3.3745 mL |