Seventeen (un)substituted N-[4-(propyl)cyclohexyl]-amides (6a-h, 7a-h and 8
) were synthesized and rested as anti-inflammatory and analgesic agents. Th
e substituents on the aromatic ring were chosen in order to study the influ
ence of electron-withdrawing or electron-donating residues, that change the
electronic density on the aromatic moiety. The pharmacological results all
ow drawing some preliminary considerations on structure-activity relationsh
ips. (C) 2000 Elsevier Science S.A. All rights reserved.