JNJ-632

JNJ-632 Suppliers list
Company Name: Jia Xing Isenchem Co.,Ltd  
Tel: 0573-85285100 18627885956
Email: isenchem@163.com
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
Email:
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: ShangHai Biochempartner Co.,Ltd  
Tel: 177-54423994 17754423994
Email: 2853530910@QQ.com

JNJ-632 manufacturers

  • JNJ-632
  • JNJ-632 pictures
  • $64.00
  • 2026-04-22
  • CAS:1572510-42-9
  • Purity: 99.17%
  • Supply Ability: 10g
JNJ-632 Basic information
Product Name:JNJ-632
Synonyms:JNJ-632;JNJ-632; JNJ 632; JNJ632;CS-2776;N-(4-fluoro-3-methyl-phenyl)-3-[[(3S)-tetrahydrofuran-3-yl]sulfamoyl]benzamide;N-(4-fluoro-3-methylphenyl)-3-[[(3S)-oxolan-3-yl]sulfamoyl]benzamide;Benzamide, N-(4-fluoro-3-methylphenyl)-3-[[[(3S)-tetrahydro-3-furanyl]amino]sulfonyl]-;N-(4-Fluoro-3-methylphenyl)-3-[[[(3S)-tetrahydro-3-furanyl]amino]sulfonyl]benzamide;(S)-N-(4-Fluoro-3-methylphenyl)-3-(N-(tetrahydrofuran-3-yl)sulfamoyl)benzamide
CAS:1572510-42-9
MF:C18H19FN2O4S
MW:378.42
EINECS:
Product Categories:API
Mol File:1572510-42-9.mol
JNJ-632 Structure
JNJ-632 Chemical Properties
density 1.39±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Ethanol:76.0(Max Conc. mg/mL);200.84(Max Conc. mM)
form A crystalline solid
pka10.37±0.20(Predicted)
color White to off-white
Safety Information
MSDS Information
JNJ-632 Usage And Synthesis
UsesJNJ-632 is a hepatitis B virus (HBV) capsid assembly modulator (CAM).
in vivo

The single dose PK profile of JNJ-632 is evaluated in C57BL/6 mice following intravenous (iv) and oral (po) administration. JNJ-632 has a moderate plasma clearance of 34 mL/min/kg and a moderate volume of distribution of 1.3 L/kg. The oral bioavailability is 40% following oral administration of 10 mg/kg and 66% following oral administration of 50 mg/kg. JNJ-632 has moderate terminal elimination half-life with t1/2s of 0.42±0.06 h, 1.1±0.67 h, 2.4±2.3 h, and 5.3±0.1 h for 2.5 mg/kg (iv), 10 mg/kg (po), 50 mg/kg (po), and 50 mg/kg (sc).To circumvent the first pass metabolism, JNJ-632 is also 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[1].

References[1] Vandyck K, et al. Synthesis and Evaluation of N-Phenyl-3-sulfamoyl-benzamide Derivatives as Capsid Assembly Modulators Inhibiting Hepatitis B Virus (HBV). J Med Chem. 2018 Jul 26;61(14):6247-6260. DOI:10.1021/acs.jmedchem.8b00654
JNJ-632 Preparation Products And Raw materials
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