药物发现
仿形(计算机编程)
激酶
计算生物学
效力
吞吐量
高通量筛选
药品
计算机科学
药理学
化学
生物信息学
生物
生物化学
体外
操作系统
电信
无线
作者
David Goldstein,Nathanael S. Gray,Patrick P. Zarrinkar
摘要
To fully exploit the potential of kinases as drug targets, novel strategies for the efficient discovery of inhibitors are required. In contrast to the traditional, linear process of inhibitor discovery, high-throughput kinase profiling enables a parallel approach by interrogating compounds against hundreds of targets in a single screen. Compound potency and selectivity are determined simultaneously, providing a choice of targets to pursue that is guided by the quality of lead compounds available, rather than by target biology alone.
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