生物正交化学
小分子
药物发现
化学生物学
计算生物学
化学
蛋白质组
化学基因学
组合化学
纳米技术
生物化学
生物
点击化学
材料科学
作者
Anuradha S. Raghavan,Howard C. Hang
标识
DOI:10.1016/j.drudis.2008.09.014
摘要
Chemical probes that target specific protein families offer powerful tools to accelerate drug discovery. Small molecules modified with uniquely reactive functional groups and detection tags provide novel tools to characterize complex proteomes functionally and also to help determine the specificity of small molecule inhibitors toward various enzyme/protein classes. This review highlights the application of bioorthogonal chemistries in combination with chemical probes, which together are offering unprecedented opportunities to dissect the functions of enzyme/protein families in vivo and enabling more precise target identification of small molecules. Advances in chemical probes and bioorthogonal reactions are poised to reveal new therapeutic targets and to facilitate the discovery and characterization of small molecules aimed at disease.
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