The Chemical Basis of Pharmacology

被引:81
作者
Keiser, Michael J. [1 ]
Irwin, John J. [1 ]
Shoichet, Brian K. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94158 USA
基金
美国国家卫生研究院;
关键词
ADVERSE DRUG-REACTIONS; BINDING-SITES; TARGET IDENTIFICATION; SIMILARITY METHOD; CONNECTIVITY MAP; SMALL MOLECULES; PREDICTION; DATABASE; SEARCH; N; N-DIMETHYLTRYPTAMINE;
D O I
10.1021/bi101540g
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Molecular biology now dominates pharmacology so thoroughly that ills difficult to recall that only a generation ago the field was very different. To understand drug action today, we characterize the targets through which they act and new drug leads are discovered on the basis of target structure and function. Until the mid-1980s the information often flowed in reverse: investigators began with organic molecules and sought targets, relating receptors not by sequence or structure but by their ligands. Recently, investigators have returned to this chemical view of biology, bringing to it systematic and quantitative methods of relating targets by their ligands. This has allowed the discovery of new targets for established drugs, suggested the bases for their side effects, and predicted the molecular targets underlying phenotypic screens. The bases for these new methods, some of their successes and liabilities, and new opportunities for their use are described.
引用
收藏
页码:10267 / 10276
页数:10
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