This study describes the antinociceptive activity of some N-aryl-glutaramic
acids and N-aryl-glutarimides in writhing and formalin tests, two classica
l models of pain in mice. These compounds show high activity, being more ac
tive than acetyl salycilic acid, acetaminophen and indomethacin, used as st
andard drugs for comparison. The introduction of different substituent grou
ps in the aromatic ring caused a significant change in activity. The result
s obtained here are promising from a pharmacological point of view, since t
hese simple compounds might be used as models to obtain new and potent anal
gesic drugs.