The development of non-steroidal dual in
✍
J. Blagg; S.A. Ballard; K. Cooper; P.W. Finn; P.S. Johnson; F. MacIntyre; G.N. M
📂
Article
📅
1996
🏛
Elsevier Science
🌐
English
⚖ 338 KB
The design, synthesis and biological properties of homochiral non-steroidal inhibitors of both isozymes of human 5¢t-reductase are described. The o-hydroxy aniline moiety of the initial lead (1) can be replaced by a 3-acyl indole isostere, whilst the minimum energy conformation of the benzyl ether i