Tetrahydroquinoline-based tricyclic amines as potent and selective agonists of the 5-HT2C receptor.
Bioorg Med Chem Lett
; 26(24): 5877-5882, 2016 12 15.
Article
em En
| MEDLINE
| ID: mdl-27864071
ABSTRACT
The syntheses, structure-activity relationships (SARs), and biological activities of tetrahydroquinoline-based tricyclic amines as 5-HT2C receptor agonists are reported. An early lead containing a highly unique 6,6,7-ring system was optimized for both in vitro potency and selectivity at the related 5-HT2B receptor. Orally bioactive, potent, and selective 6,6,6-tricyclic 5-HT2C agonists were identified.
Palavras-chave
Texto completo:
1
Coleções:
01-internacional
Base de dados:
MEDLINE
Assunto principal:
Quinolinas
/
Receptor 5-HT2C de Serotonina
/
Agonistas do Receptor 5-HT2 de Serotonina
/
Aminas
Limite:
Animals
Idioma:
En
Revista:
Bioorg Med Chem Lett
Assunto da revista:
BIOQUIMICA
/
QUIMICA
Ano de publicação:
2016
Tipo de documento:
Article