Biagi G, Livi O, Scartoni V
Farmaco Sci. 1987 Apr;42(4):285-97.
A number of novel alpha-[4-substituted-(1,2,3-triazole)]propionates have been prepared and tested as inhibitors of arachidonic acid-induced malondialdehyde formation in human platelets. The obtained products confirmed previous structure-activity relationships. Some of them showed moderate inhibitory activity.
已经制备了多种新型α-[4-取代-(1,2,3-三唑)]丙酸酯,并作为花生四烯酸诱导的人血小板中丙二醛形成的抑制剂进行了测试。所得产物证实了先前的构效关系。其中一些表现出中等抑制活性。