New heteroaryl-spaced phosphono α-amino acids are competitive NMDA antagonists with analgesic activity
摘要:
The synthesis and the NMDA receptor binding affinities of alpha-amino-3-(phosphonomethyl)-2-naphthalene-propanoic acid, alpha-amino-3-(phosphonomethyl)-2-benzofuranpropanoic acid, a series of substituted (R)-alpha-amino-3-(phosphonomethyl)-2-quinolinepropanoic acids, (R)-alpha-amino-3-(phosphonomethyl)-1,8-naphthyridine-2-propanoic acid and (R)-alpha-amino-3-(phosphonomethyl)-1,6-naphthyridine-2-propanoic acid are reported. Copyright (C) 1996 Elsevier Science Ltd
New heteroaryl-spaced phosphono α-amino acids are competitive NMDA antagonists with analgesic activity
作者:Britt-Marie Swahn、Alf Claesson、Benjamin Pelcman、Yevgeni Besidski、Håkan Molin、Mats P. Sandberg、Odd-Geir Berge
DOI:10.1016/0960-894x(96)00288-0
日期:1996.7
The synthesis and the NMDA receptor binding affinities of alpha-amino-3-(phosphonomethyl)-2-naphthalene-propanoic acid, alpha-amino-3-(phosphonomethyl)-2-benzofuranpropanoic acid, a series of substituted (R)-alpha-amino-3-(phosphonomethyl)-2-quinolinepropanoic acids, (R)-alpha-amino-3-(phosphonomethyl)-1,8-naphthyridine-2-propanoic acid and (R)-alpha-amino-3-(phosphonomethyl)-1,6-naphthyridine-2-propanoic acid are reported. Copyright (C) 1996 Elsevier Science Ltd
Korodi, Ference, Journal of Heterocyclic Chemistry, 1991, vol. 28, # 6, p. 1549 - 1552