Structure-based design of non-peptidic pyridone aldehydes as inhibitors of interleukin-1 beta converting enzyme.

被引:26
作者
Golec, JMC
Mullican, MD
Murcko, MA
Wilson, KP
Kay, DP
Jones, SD
Murdoch, R
Bemis, GW
Raybuck, SA
Luong, YP
Livingston, DJ
机构
[1] VERTEX PHARMACEUT INC,CAMBRIDGE,MA 02139
[2] ROUSSEL LABS LTD,SWINDON SN3 5BZ,WILTS,ENGLAND
关键词
D O I
10.1016/S0960-894X(97)00394-6
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pyridone derivatives, especially with 6-aryl substituents, have been shown to be useful P-2-P-3 peptidomimetic scaffolds for the design of potent inhibitors of ICE. (C) 1997 Elsevier Science Ltd.
引用
收藏
页码:2181 / 2186
页数:6
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