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261766-23-8

261766-23-8 Structure

261766-23-8 Structure
IdentificationBack Directory
[Name]

N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE
[CAS]

261766-23-8
[Synonyms]

N-4AIA
N-4ACETIA
N-(4-ACETAMIDOPHENYL)-INDOMETHACIN AMIDE
N-(4-ACETAMIDOPHENYL)-1-P-CHLOROBENZOYL-5-METHOXY-2-METHYLINDOLE-3-ACETAMIDE
N-(4-ACETAMIDOPHENYL)-1-(4-CHLOROBENZOYL)-5-METHOXY-2-METHYL-1H-INDOLE-3-ACETAMIDE
N-4AcetIA, N-(4-Acetamidophenyl)-1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetamide
[Molecular Formula]

C27H24ClN3O4
[MDL Number]

MFCD02683236
[MOL File]

261766-23-8.mol
[Molecular Weight]

489.95
Chemical PropertiesBack Directory
[Appearance]

Pale Yellow Solid
[Melting point ]

256-257°C
[storage temp. ]

−20°C
[solubility ]

DMSO: ≥15 mg/mL
[form ]

crystalline
[color ]

Pale Yellow
Hazard InformationBack Directory
[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
[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.
[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.
Safety DataBack Directory
[WGK Germany ]

3
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