Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)-

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Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)- manufacturers

  • LP-471756
  • LP-471756 pictures
  • $30.00
  • 2026-08-08
  • CAS:413605-11-5
  • Purity: 99.76%
  • Supply Ability: 10g
Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)- Basic information
Product Name:Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)-
Synonyms:Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)-;LP 471756;LP471756;LP-471756;LP-471756, 10 mM in DMSO;4-Cyclohexyl-N-(o-tolyl)benzenesulfonamide
CAS:413605-11-5
MF:C19H23NO2S
MW:329.46
EINECS:
Product Categories:
Mol File:413605-11-5.mol
Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)- Structure
Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)- Chemical Properties
Boiling point 473.5±48.0 °C(Predicted)
density 1.193±0.06 g/cm3(Predicted)
pka8.83±0.10(Predicted)
form Solid
color White to off-white
Safety Information
MSDS Information
Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)- Usage And Synthesis
DescriptionLP-471756 is antagonist of GPR139.
UsesLP-471756 is a potent GPR139 antagonist with an IC50 value of 640 nM. LP-471756 inhibits LP-360924-stimulated cAMP production[1][2].
References[1] Vedel L, et al. Pharmacology and function of the orphan GPR139 G protein-coupled receptor. Basic Clin Pharmacol Toxicol. 2020 Jun;126 Suppl 6(Suppl 6):35-46. DOI:10.1111/bcpt.13263
[2] Hu LA, et al. Identification of surrogate agonists and antagonists for orphan G-protein-coupled receptor GPR139. J Biomol Screen. 2009 Aug;14(7):789-97. DOI:10.1177/1087057109335744
Benzenesulfonamide, 4-cyclohexyl-N-(2-methylphenyl)- Preparation Products And Raw materials
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