作者: MG Rimoli , L Avallone , P de Caprariis , E Luraschi , E Abignente
DOI: 10.1016/S0223-5234(97)83971-2
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摘要: Summary A series of methyl-substituted imidazo[1,2- a ]pyrazines 8 bearing carboxylic acid group on the imidazole ring were synthesized. The structures new compounds confirmed by 1 H- and 13 C-NMR spectral data; correct assignment carbon resonances was made means HETCOR COLOC experiments. Antiinflammatory, analgesic ulcerogenic activities in vivo evaluated compared with those antiinflammatory imidazopyrazines ( 2 3 ) indomethacin. inhibitory action cyclooxygenase activity vitro. Compounds found to be less potent than indomethacin these assays. SARs are discussed.