G蛋白偶联受体(GPCR)是迄今为止在现代药物发现中最成功的可靶向家族。超过三分之一的已批准药物的靶向是GPCR。我们精心选择了54,080个多样化的化合物,专门针对GPCR进行靶向。所有化合物均以干粉形式存储,并可以以多种自定义格式获取。或者,我们可以迅速提供54,080个化合物的预装GPCR库副本,也可以提供定制的即用于筛选的格式。GPCR库包含54,080个化合物,旨在发现新的GPCR配体。
我们使用了多种基于计算的方法来设计我们的GPCR库。该库涵盖了广泛的GPCR靶点,并具有药物发现的最重要特征-新颖性和高多样性。我们采用了综合方法,包括基于2D指纹相似性搜索的框架、对GPCR特权骨架的精心选择以及通过3D药效团搜索进行共同结构模体的扩展,以寻找潜在的活性化合物。在合并的化合物池中应用了药物化学优化,最终得到了一组独特的54,500个高质量小分子化合物。
https://enamine.net/compound-libraries/targeted-libraries/gpcr-library
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