Design and syntheses of diarylisoxazoles: Novel inhibitors of cyclooxygenase-2 (COX-2) with analgesic-antiinflammatory activity

A group of 4,5-diphenylisoxazoles (11a-p), 3,4-diphenyl-5-trifluoromethylis oxazoles (15, 21), and 4,5-diphenyl-3-methylsulfonamidoisoxazole (23) posse ssing a variety of substituents (H, F, MeS, MeSO, MeSO2) at the para-positi on of one of the phenyl rings were synthesized for evaluation as analgesic, and selective COX-2 inhibitory antiinflammatory (Al), agents. Although the 3,5-diphenylisoxazole group of compounds (11a-p) exhibited potent analgesi c and Al activities, those compounds evaluated (11a, 11b, 11m) were more se lective inhibitors of COX-1 than COX-2, with the exception of 4-(4-methylsu lphonylphenyl)-5-phenylisoxazole (11n) that showed a modest COX-2 selectivi ty index (SI) of 2.1. In contrast, 3-(4-methylsulphonylphenyl)-4-phenyl-5-t rifluoromethylisoxazole (15), which retained good analgesic and AI activiti es, was a highly potent and selective COX-2 inhibitor (COX-1 IC50 > 500 muM ; COX-2 IC50 < 0.001 <mu>M) with a COX-2 SI of > 500,000, relative to the r eference drug celecoxib (COX-1 IC50 = 22.9 muM; COX-2 IC50 = 0.0567 muM) wi th a COX-2 SI of 404. The 3-phenyl-4-(4-methylsulphonylphenyl) regioisomer (21) was a less potent inhibitor (COX-1 IC50 = 252 muM; COX-2 IC50 = 0.2236 (muM) with a COX-2 SI of 1122, relative to the regioisomer (15). The relat ed compound 4,5-diphenyl-3-methylsulfonamidoisoxazole (23) exhibited simila r (to 21) potency and COX-2 selectivity (COX-1 IC50 > 200 muM; COX-2 IC50 = 0.226 muM) with an SI of 752. A molecular modeling (docking) study for the most potent, and selective, COX-2 inhibitor (15) in the active site of the human COX-2 enzyme showed the C-5 CF3 substituent is positioned 3.37 Angst rom from the phenolic OH of Tyr(355), and 6.91 Angstrom from the Ser(530) O H. The S-atom of the MeSO2 substituent is positioned deep (7.40 Angstrom fr om the entrance) inside the COX-2 secondary pocket (Val(523)). These studie s indicate a C-5 CF3 (15, 21), or C-3 NHSO2Me (23), central isoxazole ring substituent is crucial to selective inhibition of COX-2 for this class of c ompounds. (C) 2001 Wiley-Liss, Inc.