Use of the X-ray structure of the β2-adrenergic receptor for drug discovery.: Part 2:: Identification of active compounds

被引:71
作者
Sabio, Michael [1 ]
Jones, Kenneth [1 ]
Topiol, Sid [1 ]
机构
[1] Lundbeck Res USA, Paramus, NJ 07652 USA
关键词
beta(2)-adrenergic receptor; GPCR; timolol; high-throughput docking; carvedilol; Corazolol;
D O I
10.1016/j.bmcl.2008.09.046
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The recently published X-ray structures of the beta(2)-adrenergic receptor are the first examples of ligand-mediated GPCR crystal structures. We have previously performed computational studies that examine the potential viability of these structures for use in drug design, exploiting known ligand activities. Our previous study and a newly reported beta(2)/Timolol X-ray complex provide validation of the computational approaches. In the present work, we use the X-ray structures to extract, via in silico high-throughput docking, compounds from proprietary and commercial databases and demonstrate the successful identification of active compounds by radioligand binding. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5391 / 5395
页数:5
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