Potent quinoxaline-spaced phosphono. alpha.-amino acids of the AP-6 type as competitive NMDA antagonists: synthesis and biological evaluation
…, LP Greenblatt, IL Jirkovsky, M Conklin…
Index: Baudy, Reinhardt B.; Greenblatt, Lynne P.; Jirkovsky, Ivo L.; Conklin, Mary; Russo, Ralph J.; et al. Journal of Medicinal Chemistry, 1993 , vol. 36, # 3 p. 331 - 342
Full Text: HTML
Citation Number: 58
Abstract
A series of a-amino-3-(phosphonoalkyl)-2-quinoxalinepropanoic acids was synthesized and evaluated for NMDA receptor affinity using a [3Hl CPP binding assay. Functional antagonism of the NMDA receptor complex was evaluated in vitro using a stimulated [3HlTCP binding assay and in vivo by employing an NMDA-induced seizure model. Some analogues also were evaluated in the I3H1-glycine binding assay. Several compounds of ...
Related Articles:
Synthesis of some substituted quinoxalines and polycyclic systems containing the quinoxaline nucleus
[Ahmad, Abid R.; Mehta, Lina K.; Parrick, John Journal of the Chemical Society - Perkin Transactions 1, 1996 , # 20 p. 2443 - 2449]