Structure-Based Discovery of Novel Ligands for the Orexin 2 Receptor

被引:8
|
作者
Gunera, Jakub [1 ]
Baker, Jillian G. [2 ]
van Hilten, Niek [1 ]
Rosenbaum, Daniel M. [3 ,4 ]
Kolb, Peter [1 ]
机构
[1] Philipps Univ, Dept Pharmaceut Chem, D-35032 Marburg, Hesse, Germany
[2] Univ Nottingham, Queens Med Ctr, Cell Signalling, Sch Life Sci, Nottingham NG7 2UH, England
[3] UT Southwestern Med Ctr, Dept Biophys, Dallas, TX 75390 USA
[4] UT Southwestern Med Ctr, Dept Biochem, Dallas, TX 75390 USA
关键词
BETA(2)-ADRENERGIC RECEPTOR; BINDING; DOCKING; ANTAGONIST;
D O I
10.1021/acs.jmedchem.0c00964
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The orexin receptors are peptide-sensing G protein-coupled receptors that are intimately linked with regulation of the sleep/wake cycle. We used a recently solved X-ray structure of the orexin receptor subtype 2 in computational docking calculations with the aim to identify additional ligands with unprecedented chemotypes. We found validated ligands with a high hit rate of 29% out of those tested, none of them showing selectivity with respect to the orexin receptor subtype 1. Furthermore, of the higher-affinity compounds examined, none showed any agonist activity. While novel chemical structures can thus be found, selectivity is a challenge owing to the largely identical binding pockets.
引用
收藏
页码:11045 / 11053
页数:9
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