| Literature DB >> 26099069 |
Delphine Karila1, Thomas Freret2, Valentine Bouet2, Michel Boulouard2, Patrick Dallemagne1, Christophe Rochais1.
Abstract
Given its predominant expression in the central nervous system (CNS), 5-hydroxytryptamine (5-HT: serotonin) subtype 6 receptor (5-HT6R) has been considered as a valuable target for the development of CNS drugs with limited side effects. After 2 decades of intense research, numerous selective ligands have been developed to target this receptor; this holds potential interest for the treatment of neuropathological disorders. In fact, some agents (mainly antagonists) are currently undergoing clinical trial. More recently, a series of potent and selective agonists have been developed, and preclinical studies have been conducted that suggest the therapeutic interest of 5-HT6R agonists. This review details the medicinal chemistry of these agonists, highlights their activities, and discusses their potential for treating cognitive issues associated with Alzheimer's disease (AD), depression, or obesity. Surprisingly, some studies have shown that both 5-HT6R agonists and antagonists exert similar procognitive activities. This article summarizes the hypotheses that could explain this paradox.Entities:
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Year: 2015 PMID: 26099069 DOI: 10.1021/acs.jmedchem.5b00179
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446