Enantiospecific, selective cyclooxygenase-2 inhibitors

Enantiospecific, selective cyclooxygenase-2 inhibitors Structural Basis of Enantioselective Inhibition of Cyclooxygenase-1 by S-α-Substituted Indomethacin Ethanolamides Ester and Amide Derivatives of the Nonsteroidal Antiinflammatory Drug, Indomethacin, as Selective Cyclooxygenase-2 Inhibitors Synthesis and biological evaluation of both enantiomers of L-761,000 as inhibitors of cyclooxygenase 1 and 2 From indomethacin to a selective COX-2 inhibitor: Development of indolalkanoic acids as potent and selective cyclooxygenase-2 inhibitors A new class of acyclic 2-alkyl-1,2-diaryl (E)-olefins as selective cyclooxygenase-2 (COX-2) inhibitors The 2′-Trifluoromethyl Analogue of Indomethacin Is a Potent and Selective COX-2 Inhibitor Thiazole analogues of the NSAID indomethacin as selective COX-2 Inhibitors Synthesis and evaluation of carbaborane derivatives of indomethacin as cyclooxygenase inhibitors Structural modification of indomethacin toward selective inhibition of COX-2 with a significant increase in van der Waals contributions