Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester

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Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester Basic information
Product Name:Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester
Synonyms:Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester;P2Y2R/GPR17 antagonist 1;P2Y2R/GPR17 antagonist 1, 10 mM in DMSO;NN1213 acetate
CAS:2395016-49-4
MF:C19H13ClN2O6S
MW:432.83
EINECS:
Product Categories:
Mol File:2395016-49-4.mol
Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester Structure
Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester Chemical Properties
Boiling point 548.3±50.0 °C(Predicted)
density 1.514±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : 125 mg/mL (288.80 mM; Need ultrasonic)
pka11.68±0.70(Predicted)
form Solid
color Light yellow to yellow
Safety Information
MSDS Information
Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester Usage And Synthesis
UsesP2Y2R/GPR17 antagonist 1 (Compound 14m) is a dual P2Y2R and GPR17 antagonist with IC50 values of 3.17 μM and 1.67 μM against P2Y2R and GPR17, respectively. P2Y2R/GPR17 antagonist 1 shows excellent metabolic stability in human liver microsomes[1].
References[1] Pillaiyar T, et al. Design, synthesis and biological evaluation of suramin-derived dual antagonists of the proinflammatory G protein-coupled receptors P2Y2 and GPR17. Eur J Med Chem. 2020 Jan 15;186:111789. DOI:10.1016/j.ejmech.2019.111789
Benzenesulfonic acid, 4-[(2-chlorobenzoyl)amino]-, 3-nitrophenyl ester Preparation Products And Raw materials
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