European Journal of Medicinal Chemistry p. 163 - 170 (1998)
Update date:2022-08-16
Topics:
Laneri, Sonia
Sacchi, Antonia
Gallitelli, Marina
Arena, Francesca
Luraschi, Elena
Abignente, Enrico
Filippelli, Walter
Rossi, Francesco
The synthesis of a group of 2-methylimidazo[1,2-a]pyrimidine-3-carboxylic esters, acids and amides is described. The structures of new compounds are supported by 1H and 13C NMR spectra. These compounds were tested in vivo for their antiinflammatory analgesic and ulcerogenic activity. Eight new compounds out of fifteen showed remarkable dose-dependent antiinflammatory action in die carrageenan rat paw edema (1/2-1/3 x indomethacin) but weak analgesic activity in the acetic acid writhing test together with negligible ulcerogenic action. The new compounds were found to be lacking in inhibitory activity on cyclooxygenase in vitro.
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