Solid-phase compound library synthesis in drug design and development

被引:0
|
作者
Edwards, PJ [1 ]
Morrell, AI [1 ]
机构
[1] Pfizer Global Res & Dev, Lib Design & Prod Grp, Sandwich CT13 9NJ, Kent, England
关键词
compound library; drug discovery; lead optimization; parallel synthesis; solid-phase organic synthesis;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This article is a subjective review of the literature between December 2000 and January 2002 related to the solid-phase synthesis of compound libraries for drug discovery and development. Examples of libraries yielding active compounds across a range of biological tar-gets are presented, together with synthetic details where this is deemed of sufficient note. Background to the biological target and any structure-activity relationship, which can be discerned within members of a library series, is also discussed. A brief overview of new developments in solid-phase technology that is likely to impact upon drug discovery is also included.
引用
收藏
页码:594 / 605
页数:12
相关论文
共 50 条