Synthesis, glycine NMDA and AMPA binding activity of some new 2,5,6-trioxopyrazino[1,2,3-de]quinoxalines and of their restricted analogs 2,5-dioxo- and 4,5-dioxoimidazo[1,5,4-de] quinoxalines

Citation
F. Varano et al., Synthesis, glycine NMDA and AMPA binding activity of some new 2,5,6-trioxopyrazino[1,2,3-de]quinoxalines and of their restricted analogs 2,5-dioxo- and 4,5-dioxoimidazo[1,5,4-de] quinoxalines, ARCH PHARM, 332(6), 1999, pp. 201-207
Citations number
14
Categorie Soggetti
Pharmacology & Toxicology
Journal title
ARCHIV DER PHARMAZIE
ISSN journal
03656233 → ACNP
Volume
332
Issue
6
Year of publication
1999
Pages
201 - 207
Database
ISI
SICI code
0365-6233(199906)332:6<201:SGNAAB>2.0.ZU;2-R
Abstract
The synthesis of some new 1,2,3,5,6,7-hexahydro-2,5,6-trioxopyrazino[1,2,3- de]quinoxalines 1c-g and of their restricted analogs 2,4,5,6-tetrahydro-2,5 -dioxo-1H-2a-g and 5,6-dihydro-4,5-dioxo-4H-imidazo[1,5,4-de]quinoxaline 3a -d is reported. Compounds 1c-g, 2a-g, and 3a-d were tested for their bindin g activity at the glycine/NMDA and AMPA receptors. The results thar only th e 6,6,6-tricyclic derivatives 1c-g are able to bind glycine/NMDA and AMPA r eceptors, although with lower affinity than the previously reported lead co mpounds 1a-b. In contrasts, the 5,6,6-tricyclic derivatives 2a-g are inacti ve at both receptors and only one 4,5-dioxoimidazoquinoxaline (3b) displays a weak glycine/NMDA receptor affinity.