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JNJ-632

Cat. No. M9119

All AbMole products are for research use only, cannot be used for human consumption.

JNJ-632 Structure
Synonym:

JNJ632

Size Price Availability Quantity
10mM*1mL in DMSO USD 88 In stock
5mg USD 80 In stock
10mg USD 120 In stock
25mg USD 240 In stock
50mg USD 385 In stock
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Quality Control & Documentation
Biological Activity

JNJ-632 is a potent HVV capsid assembly modulator and HBV replication inhibitor with EC50 of 100-200 nM for genotypes A-D. JNJ-632 inhibits HBV DNA HepG2.2.15 and HBV DNA HepG2.117 with EC50s of 0.12 and 0.43 μM, respectively. In the high-content multiparameter cytotoxicity (HepG2), JNJ-632 shows EC20s in the 10-30 μM range (considered weakly cytotoxic).

In vivo, JNJ-632 is dosed subcutaneously at 50 mg/kg in C57BL/6 mice and this results in a concentration in plasma after 24 h of dosing of 102 ng/mL and concentration in liver after 24 h of dosing of 1297 ng/g.

Chemical Information
Molecular Weight 378.42
Formula C18H19FN2O4S
CAS Number 1572510-42-9
Solubility (25°C) DMSO: ≥ 80 mg/mL (Need ultrasonic)
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Vandyck K, et al. J Med Chem. Synthesis and Evaluation of N-Phenyl-3-sulfamoyl-benzamide Derivatives as Capsid Assembly Modulators Inhibiting Hepatitis B Virus (HBV).

[2] Berke JM, et al. Antimicrob Agents Chemother. Capsid Assembly Modulators Have a Dual Mechanism of Action in Primary Human Hepatocytes Infected with Hepatitis B Virus.

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Keywords: JNJ-632, JNJ632 supplier, Anti-infection, inhibitors, activators

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