Author/Authors :
Horng-Chih Huang، نويسنده , , Timothy S. Chamberlain، نويسنده , , Karen Selbert، نويسنده , , Carol M. Koboldt، نويسنده , , Peter C. Isakson، نويسنده , , David B. Reitz، نويسنده ,
Abstract :
Novel series of diaryl indenes and benzofurans have been shown to be potent and selective COX-2 inhibitors. A structure-activity relationship study suggests that the conversion of sulfones to sulfonamides affords potent, but slightly less selective COX-2 inhibitors, and that for benzofurans the 3-halo-4-methoxyphenyl sulfonamide analogs are more selective than the corresponding 4-fluorophenyl analog.