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N-(4-Acetamidophenyl)indomethacinamide_Molecular_structure_CAS_)
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N-(4-Acetamidophenyl)indomethacinamide

Catalog No. A1224 Name Sigma Aldrich
CAS Number Website http://www.sigmaaldrich.com
M. F. C27H24ClN3O4 Telephone 1-800-521-8956
M. W. 489.95016 Fax
Purity ≥98% Email
Storage Chembase ID: 155694

SYNONYMS

IUPAC name
2-[1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indol-3-yl]-N-(4-acetamidophenyl)acetamide
IUPAC Traditional name
2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]-N-(4-acetamidophenyl)acetamide
Synonyms
N-(4-Acetamidophenyl)-1-(4-chlorobenzoyl)-5-methoxy-2-methyl-1H-indole-3-acetamide
N-4AcetIA

DATABASE IDS

MDL Number MFCD02683236

PROPERTIES

Empirical Formula (Hill Notation) C27H24N3O4Cl
Purity ≥98%
Shipped in wet ice
Absorption Wavelength λmax 267 nm
Apperance crystalline
Solubility DMSO: ≥15 mg/mL
Solubility DMF: ≥23 mg/mL
MSDS Link Download
Personal Protective Equipment Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Storage Temperature -20°C
German water hazard class 3

DETAILS

Description (English)
Biochem/physiol Actions
Potent and selective reversible COX-2 inhibitor. N-4-AcetIA inhibits human and ovine COX-2 with IC50 of 0.1 μM and 0.625 μM, respectively. About 400 times less potent as an inhibitor of human COX-1 and 80 times less potent as an inhibitor of ovine COX-1. Shows anti-inflammatory, antiangiogenic, and cancer chemopreventive activity in various experimental models.
Description (简体中文)
Biochem/physiol Actions
Potent and selective reversible COX-2 inhibitor. N-4-AcetIA inhibits human and ovine COX-2 with IC50 of 0.1 μM and 0.625 μM, respectively. About 400 times less potent as an inhibitor of human COX-1 and 80 times less potent as an inhibitor of ovine COX-1. Shows anti-inflammatory, antiangiogenic, and cancer chemopreventive activity in various experimental models.

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