Applications of chemogenomic library screening in drug discovery

被引:115
|
作者
Jones, Lyn H. [1 ]
Bunnage, Mark E. [1 ,2 ]
机构
[1] Pfizer, Med Design, 610 Main St, Cambridge, MA 02139 USA
[2] Vertex Pharmaceut, 50 Northern Ave, Boston, MA 02210 USA
关键词
DUCHENNE MUSCULAR-DYSTROPHY; TARGET IDENTIFICATION; SMALL MOLECULES; KINASE INHIBITORS; CHEMICAL BIOLOGY; IN-VIVO; MYELOID-LEUKEMIA; CANCER; CELLS; REVEALS;
D O I
10.1038/nrd.2016.244
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The allure of phenotypic screening, combined with the industry preference for target-based approaches, has prompted the development of innovative chemical biology technologies that facilitate the identification of new therapeutic targets for accelerated drug discovery. A chemogenomic library is a collection of selective small-molecule pharmacological agents, and a hit from such a set in a phenotypic screen suggests that the annotated target or targets of that pharmacological agent may be involved in perturbing the observable phenotype. In this Review, we describe opportunities for chemogenomic screening to considerably expedite the conversion of phenotypic screening projects into target-based drug discovery approaches. Other applications are explored, including drug repositioning, predictive toxicology and the discovery of novel pharmacological modalities.
引用
收藏
页码:285 / 296
页数:12
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