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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  USD88 In stock
5mg USD 80  USD80 In stock
10mg USD 120  USD120 In stock
25mg USD 240  USD240 In stock
50mg USD 385  USD385 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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