Nonpeptide Urotensin-II receptor agonists and antagonists: Review and structure-activity relationships

被引:22
|
作者
Lescot, Elodie [1 ]
Bureau, Ronan [1 ]
Rault, Sylvain [1 ]
机构
[1] Univ Caen, UFR Sci Pharmaceut, Ctr Etudes & Rech Medicament Normandie, F-14032 Caen, France
关键词
Urotensin-II; GPR14; nonpeptide agonists and antagonists; GPCR; SAR; pharmacophore;
D O I
10.1016/j.peptides.2007.09.019
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human Urotensin-II (hU-II) is a cyclic 11-amino acid peptide that plays a role in cardiovascular homeostasis. Its receptor is a member of the class A of G-protein-coupled receptors, called GPR14. In recent years, several nonpeptide ligands have been reported in the literature. Most were identified by high-throughput screening and optimized by medicinal chemistry methods. Other nonpeptide ligands were discovered starting from the 3D structure of hU-II or other ligands. They were identified by a virtual screening approach based on a 3D pharmacophore or by structural similarity with others cyclic peptides. in this review, nonpeptide agonists and antagonists are presented in relation to structure-activity relationships. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:680 / 690
页数:11
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