Basic information Safety Supplier Related

N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE

Basic information Safety Supplier Related

N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE Basic information

Product Name:
N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE
Synonyms:
  • N-(4-ACETAMIDOPHENYL)-1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETAMIDE
  • N-(4-ACETAMIDOPHENYL)-1-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETAMIDE
  • N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE
  • N-4ACETIA
  • N-4AIA
  • N-4AcetIA, N-(4-Acetamidophenyl)-1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetamide
  • 1H-Indole-3-acetamide, N-[4-(acetylamino)phenyl]-1-(4-chlorobenzoyl)-5-methoxy-2-methyl-
CAS:
261766-23-8
MF:
C27H24ClN3O4
MW:
489.95
Product Categories:
  • Inhibitors
  • Aromatics
  • Heterocycles
Mol File:
Mol File
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N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE Chemical Properties

Melting point:
256-257°C
storage temp. 
−20°C
solubility 
DMSO: ≥15 mg/mL
form 
crystalline
color 
Pale Yellow
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Safety Information

WGK Germany 
3

MSDS

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N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE Usage And Synthesis

Description

N-(4-acetamidophenyl)-indomethacin amide (N-4-AIA) is one of several aromatic amides of indomethacin reported to be potent and selective reversible inhibitors of COX-2. N-4-AIA inhibits human recombinant and ovine COX-2 with IC50 values of 0.12 and 0.625 μM, respectively. It is about 400 times less potent as an inhibitor of human recombinant COX-1 and 80 times less potent as an inhibitor of ovine COX-1 than ovine COX-2.

Chemical Properties

Pale Yellow Solid

Uses

An aromatic amide of indomethacin recently reported to be a potent and selective reversible inhibitor of COX-2. Inhibits human recombinant and ovine COX-2 with IC50 of 0.1 uM and 0.625 uM, respectively

Definition

ChEBI: N-(4-acetamidophenyl)-Indomethacin amide is a N-acylindole.

References

[1]. kalgutkar as, marnett ab, crews bc, et al. ester and amide derivatives of the nonsteroidal antiinflammatory drug, indomethacin, as selective cyclooxygenase-2 inhibitors. j med chem. 2000 jul 27;43(15):2860-70.

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