可药性
药物发现
离子通道
纳米技术
计算生物学
计算机科学
化学
生物信息学
材料科学
生物
生物化学
基因
受体
出处
期刊:Combinatorial Chemistry & High Throughput Screening
[Bentham Science]
日期:2008-03-01
卷期号:11 (3): 185-194
被引量:21
标识
DOI:10.2174/138620708783877735
摘要
Ion channels are a large superfamily of membrane proteins that pass ions across membranes. They are critical to diverse physiological functions in both excitable and nonexcitable cells and underlie many diseases. As a result, they are an important target class which is proven to be highly “druggable”. However, for high throughput screening (HTS), ion channels are historically difficult as a target class due to their unique molecular properties and the limitations of assay technologies that are HTS-amendable. In this article, we describe the background of ion channels and current status and challenges for ion channel drug discovery, followed by an overview of both conventional and newly emerged ion channel screening technologies. The critical impact of such new technologies on current and future ion channel drug discovery is also discussed. Keywords: Ion channel, automated patch clamp, high throughput screening, electrophysiology, drug discovery
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