Passarotti C, Bandi G L, Citerio L, Valenti M
Formenti Group, Research Laboratories, Origgio, Italy.
Boll Chim Farm. 1991 Jan;130(1):22-5.
During a search on PG-like compounds as antiulcer drugs we synthetized some hetherocyclic derivatives. Some compounds of this series were found to be effective after oral administration in inhibiting restraint induced ulcers in the rat. Three of the most active compounds showed fairly good antiinflammatory activity in the carrageenin-induced rat paw oedema test and in the RPAR test.
在对类前列腺素(PG)样化合物作为抗溃疡药物进行研究期间,我们合成了一些杂环衍生物。发现该系列中的一些化合物经口服给药后可有效抑制大鼠的束缚诱导型溃疡。其中三种活性最强的化合物在角叉菜胶诱导的大鼠足爪水肿试验和反向被动 Arthus 反应(RPAR)试验中显示出相当良好的抗炎活性。