Chemical genomics as an emerging paradigm for postgenomic drug discovery

被引:15
作者
Salemme, FR [1 ]
机构
[1] Three Dimens Pharmaceut Inc, Lower Makefield Corp Ctr 3, Yardley, PA 19067 USA
关键词
chemical genomics; drug discovery; target validation; high-throughput screening; combinatorial chemistry; pharmaceutical productivity;
D O I
10.1517/phgs.4.3.257.22692
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chemical genomics approaches are evolving to overcome key problems limiting the efficiency of drug discovery in the postgenomic era. Many of these stem from the low success rates in finding drugs for novel genomics targets whose biochemical properties and therapeutic relevance is poorly understood. The fundamental objective of chemical genomics is to find and optimize chemical compounds that can be used to directly test the therapeutic relevance of new targets revealed through genome sequencing. An integrated approach to chemical genomics encompasses a diverse set of tools including quantitative affinity-based screens, computer-directed combinatorial chemistry, and structure-based drug design. The approach is most effectively applied across targets classes whose members are structurally related, and where some members are known to have bona fide therapeutic relevance.
引用
收藏
页码:257 / 267
页数:11
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