New Orally Active Enkephalinase Inhibitors: Their Synthesis, Biological Activity, And Analgesic Properties

K Senokuchi,H Nakai, Y Nagao,Y Sakai, N Katsube,M Kawamura

BIOORGANIC & MEDICINAL CHEMISTRY(1998)

引用 19|浏览2
暂无评分
摘要
A series of (4S)-4-[(2S)-benzyl-3-mercaptopropionylamino]-4-(N-phenylcarbamoyl)-butyric acids has been identified as potent systemically active enkephalinase inhibitors. Structure-activity relationships (SAR) are discussed. Further chemical modification of the inhibitors was carried out in order to identify the inhibitors which are orally active in an animal model. Compounds of particular interest are the prodrug-like analogues, including 5b (ONO-9902). Their analgesic effects after oral administration were evaluated. (C) 1998 Elsevier Science Ltd. All rights reserved.
更多
查看译文
关键词
structure activity relationship,chemical modification,biological activity
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要