Searching new targets for anti-inflammatory drug design, agents with the isoindole skeleton were focused on the basis of preliminary studies of NSAIDs as COX-1 and/or COX-2 enzyme inhibitors.Thus several novel N-substituted isoindoline derivatives as possible biologically active compounds were prepared as analogues of Indoprofen (1) starting from cis-2-[(4methylphenyl)carbonyl]cyclohexanecarboxylic acid (3) by treatment with primary arylamines.
No takes yet. Share an insight, caveat, or question.
Csende et al. (2013) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: