Saltar al contenido
Merck

Selective COX-2 inhibitors. Part 1: synthesis and biological evaluation of phenylazobenzenesulfonamides.

Bioorganic & medicinal chemistry letters (2006-07-04)
Wei-Jern Tsai, Young-Ji Shiao, Shwu-Jiuan Lin, Wen-Fei Chiou, Lie-Chwen Lin, Tsang-Hsiung Yang, Che-Ming Teng, Tain-Shung Wu, Li-Ming Yang
RESUMEN

A series of phenylazobenzenesulfonamide derivatives were designed and synthesized for the evaluation as selective cyclooxygenase-2 (COX-2) inhibitors in a cellular assay using human whole blood (HWB) and an enzymatic assay using purified ovine enzymes. Extensive structure-activity relationships (SAR) were studied within this series, and several of selective COX-2 inhibitors have been identified. Among them, compound 8, 4-(4-amino-2-methylsulfanyl-phenylazo)benzenesulfonamide, showed a potent inhibitory activity to the cyclooxygenase enzymes (IC(50)'s for COX-1: 23.28 microM; COX-2: 2.04 microM), being active but less COX-2 selective than celecoxib.

MATERIALES
Referencia del producto
Marca
Descripción del producto

Sigma-Aldrich
Resveratrol, ≥99% (HPLC)
Sigma-Aldrich
Indomethacin, 98.5-100.5% (in accordance with EP)
Sigma-Aldrich
Indomethacin, meets USP testing specifications
Supelco
Resveratrol, analytical standard
Sigma-Aldrich
3-(Methylthio)aniline, 97%