Structure-activity relationships of serotonin 5-HT7 receptors ligands: A review

被引:13
|
作者
Thirumaran, Sangeetha-Laura [1 ]
Lepailleur, Alban [1 ]
Rochais, Christophe [1 ]
机构
[1] Normandie Univ, CERMN, UNICAEN, F-14000 Caen, France
关键词
5-HT7; receptors; Medicinal chemistry; Molecular docking; Pharmacophore; Structure-activity relationships; EXTRACELLULAR-REGULATED KINASE; ANTIDEPRESSANT-LIKE BEHAVIOR; MULTIOBJECTIVE BASED DESIGN; ACTIVATED PROTEIN-KINASE; DORSAL RAPHE NUCLEUS; EYE-MOVEMENT SLEEP; IN-VITRO; REM-SLEEP; ARYLSULFONAMIDE DERIVATIVES; ANTAGONIST SB-269970;
D O I
10.1016/j.ejmech.2019.111705
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
5-HT7 receptors are the most recently discovered serotonergic receptors, for which numerous physiological implications in the central and the peripheral nervous systems as well as the endocrine system are described. A current public health challenge is to propose new and more efficient treatments against neuropsychiatric disorders such as epilepsy or Alzheimer's disease. In this context, 5-HT7 receptors represent an interesting target for the treatment and prevention of those pathologies, as an alternative or in association with other medicines. Thus, numerous chemical series of agonists and antagonists have been developed. Some of these molecules have shown a therapeutic potential in various in vivo studies. This review aims to present an overview of 5-HT7 receptors and of the medicinal chemistry programs that led to the identification of new, potent and selective 5-HT7 receptors ligands. Structure-activity relationships studies based on molecular docking and pharmacophoric approaches are also described. (C) 2019 Elsevier Masson SAS. All rights reserved.
引用
收藏
页数:30
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