作者:Hans Peter Wolff、Hans F. Kuehnle
DOI:10.1021/jm00148a011
日期:1985.10
A series of N-alkylated 2-hydrazonopropionic acids have been synthesized and evaluated for their hypoglycemic activity. Most of the compounds exhibit a remarkable blood glucose lowering activity in fasted guinea pigs. Some of the structural variables studied were the effects of branching, unsaturation, or substitution on the alkyl side chain and the effect of nuclear substitution on the aralkyl analogues
已经合成了一系列的N-烷基化的2-肼基丙酸并评估了它们的降血糖活性。大多数化合物在禁食的豚鼠中表现出显着的降血糖活性。研究的一些结构变量是支链,不饱和键或取代基对烷基侧链的影响以及核取代基对芳烷基类似物的影响。从这些化合物中,选择2-[[[(E)-2-甲基-3-苯基-2-丙烯基] azo酰基]丙酸(BM 42.304; 42)进行进一步研究。