Abdel-Aleem A M, Abdel-Kader M A, El-Koussi A A
Pharmazie. 1980;35(7):394-8.
Some new amides of substituted oxamic acid which embody different moieties of the anti-inflammatory drugs were prepared through two routes of synthesis. The physico-chemical properties as well as the anti-inflammatory activity of these compounds were determined. Preliminary pharmacological testing revealed the superiority of most of the screened compounds as anti-inflammatory agents with relatively low toxicity as compared with acetylsalicylic acid. Correlation between structure and biological activity was suggested.
通过两条合成路线制备了一些体现抗炎药物不同部分结构的取代草氨酸新酰胺。测定了这些化合物的物理化学性质以及抗炎活性。初步药理测试表明,与乙酰水杨酸相比,大多数筛选出的化合物作为抗炎剂具有优越性,且毒性相对较低。研究表明了结构与生物活性之间的相关性。