Insights into Ligand-Elicited Activation of Human Constitutive Androstane Receptor Based on Novel Agonists and Three-Dimensional Quantitative Structure-Activity Relationship

被引:26
作者
Jyrkkarinne, Johanna [1 ]
Windshugel, Bjorn [2 ]
Ronkko, Toni [2 ]
Tervo, Ann J. [2 ]
Kublbeck, Jenni [1 ]
Lahtela-Kakkonen, Maija [2 ]
Sippl, Wolfgang [3 ]
Poso, Antti [2 ]
Honkakoski, Paavo [1 ]
机构
[1] Univ Kuopio, Dept Pharmaceut, FIN-70211 Kuopio, Finland
[2] Univ Kuopio, Dept Pharmaceut Chem, FIN-70211 Kuopio, Finland
[3] Univ Halle Wittenberg, Dept Pharm, D-06120 Halle, Saale, Germany
基金
芬兰科学院;
关键词
D O I
10.1021/jm800731b
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The human constitutive androstane receptor (CAR, NR1I3) is an important regulator of xenobiotic metabolism and other physiological processes. So far, only few CAR agonists are known and no explicit mechanism has been proposed for their action. Thus, we aimed to generate a 3D QSAR model that could explain the molecular determinants of CAR agonist action. To obtain a sufficient number of agonists that cover a wide range of activity, we applied a virtual screening approach using both structure- and ligand-based methods. We identified 27 novel human CAR agonists on which a 3D QSAR model was generated. The model, complemented by coregulator recruitment and mutagenesis results, suggests a potential activation mechanism for human CAR and may serve to predict potential activation of CAR for compounds emerging from drug development projects or for chemicals undergoing toxicological risk assessment.
引用
收藏
页码:7181 / 7192
页数:12
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