These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
82 related articles for article (PubMed ID: 13679166)
1. Benzoazepine derivative as potent antagonists of the glycine binding site associated to the NMDA receptor. Di Fabio R; Micheli F; Baraldi D; Bertani B; Conti N; Dal Forno G; Feriani A; Donati D; Marchioro C; Messeri T; Missio A; Pasquarello A; Pentassuglia G; Pizzi DA; Provera S; Quaglia AM; Sabbatini FM Farmaco; 2003 Sep; 58(9):723-38. PubMed ID: 13679166 [TBL] [Abstract][Full Text] [Related]
2. Substituted analogues of GV150526 as potent glycine binding site antagonists in animal models of cerebral ischemia. Di Fabio R; Conti N; De Magistris E; Feriani A; Provera S; Sabbatini FM; Reggiani A; Rovatti L; Barnaby RJ J Med Chem; 1999 Sep; 42(18):3486-93. PubMed ID: 10479281 [TBL] [Abstract][Full Text] [Related]
3. (E)-3-(2-(N-phenylcarbamoyl)vinyl)pyrrole-2-carboxylic acid derivatives. A novel class of glycine site antagonists. Balsamini C; Bedini A; Diamantini G; Spadoni G; Tontini A; Tarzia G; Di Fabio R; Feriani A; Reggiani A; Tedesco G; Valigi R J Med Chem; 1998 Mar; 41(6):808-20. PubMed ID: 9526557 [TBL] [Abstract][Full Text] [Related]
4. Enantiomerically pure tetrahydroquinoline derivatives as in vivo potent antagonists of the glycine binding site associated to the NMDA receptor. Di Fabio R; Tranquillini E; Bertani B; Alvaro G; Micheli F; Sabbatini F; Pizzi MD; Pentassuglia G; Pasquarello A; Messeri T; Donati D; Ratti E; Arban R; Dal Forno G; Reggiani A; Barnaby RJ Bioorg Med Chem Lett; 2003 Nov; 13(21):3863-6. PubMed ID: 14552796 [TBL] [Abstract][Full Text] [Related]
5. Tricyclic indole-2-carboxylic acids: highly in vivo active and selective antagonists for the glycine binding site of the NMDA receptor. Katayama S; Ae N; Kodo T; Masumoto S; Hourai S; Tamamura C; Tanaka H; Nagata R J Med Chem; 2003 Feb; 46(5):691-701. PubMed ID: 12593650 [TBL] [Abstract][Full Text] [Related]
6. CoMFA, synthesis, and pharmacological evaluation of (E)-3-(2-carboxy-2-arylvinyl)-4,6-dichloro-1H-indole-2-carboxylic acids: 3-[2-(3-aminophenyl)-2-carboxyvinyl]-4,6-dichloro-1H-indole-2-carboxylic acid, a potent selective glycine-site NMDA receptor antagonist. Baron BM; Cregge RJ; Farr RA; Friedrich D; Gross RS; Harrison BL; Janowick DA; Matthews D; McCloskey TC; Meikrantz S; Nyce PL; Vaz R; Metz WA J Med Chem; 2005 Feb; 48(4):995-1018. PubMed ID: 15715469 [TBL] [Abstract][Full Text] [Related]
7. Structure-activity relationships of alkyl- and alkoxy-substituted 1,4-dihydroquinoxaline-2,3-diones: potent and systemically active antagonists for the glycine site of the NMDA receptor. Cai SX; Kher SM; Zhou ZL; Ilyin V; Espitia SA; Tran M; Hawkinson JE; Woodward RM; Weber E; Keana JF J Med Chem; 1997 Feb; 40(5):730-8. PubMed ID: 9057859 [TBL] [Abstract][Full Text] [Related]
8. Synthesis and pharmacological evaluation of N-(2,5-disubstituted phenyl)-N'-(3-substituted phenyl)-N'-methylguanidines as N-methyl-D-aspartate receptor ion-channel blockers. Hu LY; Guo J; Magar SS; Fischer JB; Burke-Howie KJ; Durant GJ J Med Chem; 1997 Dec; 40(26):4281-9. PubMed ID: 9435897 [TBL] [Abstract][Full Text] [Related]
9. Novel systemically active antagonists of the glycine site of the N-methyl-D-aspartate receptor: electrophysiological, biochemical and behavioral characterization. Parsons CG; Danysz W; Quack G; Hartmann S; Lorenz B; Wollenburg C; Baran L; Przegalinski E; Kostowski W; Krzascik P; Chizh B; Headley PM J Pharmacol Exp Ther; 1997 Dec; 283(3):1264-75. PubMed ID: 9400002 [TBL] [Abstract][Full Text] [Related]
10. 4-substituted-3-phenylquinolin-2(1H)-ones: acidic and nonacidic glycine site N-methyl-D-aspartate antagonists with in vivo activity. Carling RW; Leeson PD; Moore KW; Moyes CR; Duncton M; Hudson ML; Baker R; Foster AC; Grimwood S; Kemp JA; Marshall GR; Tricklebank MD; Saywell KL J Med Chem; 1997 Feb; 40(5):754-65. PubMed ID: 9057862 [TBL] [Abstract][Full Text] [Related]
11. Syntheses and N-methyl-D-aspartate receptor antagonist pharmacology of fluorinated arylcycloheptylamines. Sun S; Wallach J; Adejare A Med Chem; 2014; 10(8):843-52. PubMed ID: 24773376 [TBL] [Abstract][Full Text] [Related]
12. In vivo models of cerebral ischemia: effects of parenterally administered NMDA receptor glycine site antagonists. Warner DS; Martin H; Ludwig P; McAllister A; Keana JF; Weber E J Cereb Blood Flow Metab; 1995 Mar; 15(2):188-96. PubMed ID: 7860652 [TBL] [Abstract][Full Text] [Related]
13. [Effects of Ginkgo biloba extract against excitotoxicity induced by NMDA receptors and mechanism thereof]. Xiao ZY; Sun CK; Xiao XW; Lin YZ; Li S; Ma H; Song GR; Cheng R Zhonghua Yi Xue Za Zhi; 2006 Sep; 86(35):2479-84. PubMed ID: 17156678 [TBL] [Abstract][Full Text] [Related]
14. SM-31900, a novel NMDA receptor glycine-binding site antagonist, reduces infarct volume induced by permanent middle cerebral artery occlusion in spontaneously hypertensive rats. Ohtani K; Tanaka H; Ohno Y Neurochem Int; 2003 Apr; 42(5):375-84. PubMed ID: 12510020 [TBL] [Abstract][Full Text] [Related]
15. Design, synthesis, SAR, and biological evaluation of highly potent benzimidazole-spaced phosphono-alpha-amino acid competitive NMDA antagonists of the AP-6 type. Baudy RB; Fletcher H; Yardley JP; Zaleska MM; Bramlett DR; Tasse RP; Kowal DM; Katz AH; Moyer JA; Abou-Gharbia M J Med Chem; 2001 May; 44(10):1516-29. PubMed ID: 11334562 [TBL] [Abstract][Full Text] [Related]
16. Novel 3-carboxy- and 3-phosphonopyrazoline amino acids as potent and selective NMDA receptor antagonists: design, synthesis, and pharmacological characterization. Conti P; Pinto A; Tamborini L; Madsen U; Nielsen B; Bräuner-Osborne H; Hansen KB; Landucci E; Pellegrini-Giampietro DE; De Sarro G; Donato Di Paola E; De Micheli C ChemMedChem; 2010 Sep; 5(9):1465-75. PubMed ID: 20665761 [TBL] [Abstract][Full Text] [Related]
17. Characterization of indole-2-carboxylate derivatives as antagonists of N-methyl-D-aspartate receptor activity at the associated glycine recognition site. Hood WF; Gray NM; Dappen MS; Watson GB; Compton RP; Cordi AA; Lanthorn TH; Monahan JB J Pharmacol Exp Ther; 1992 Aug; 262(2):654-60. PubMed ID: 1386886 [TBL] [Abstract][Full Text] [Related]
18. Hydantoin-substituted 4,6-dichloroindole-2-carboxylic acids as ligands with high affinity for the glycine binding site of the NMDA receptor. Jansen M; Potschka H; Brandt C; Löscher W; Dannhardt G J Med Chem; 2003 Jan; 46(1):64-73. PubMed ID: 12502360 [TBL] [Abstract][Full Text] [Related]
19. LU 73068, a new non-NMDA and glycine/NMDA receptor antagonist: pharmacological characterization and comparison with NBQX and L-701,324 in the kindling model of epilepsy. Potschka H; Löscher W; Wlaź P; Behl B; Hofmann HP; Treiber HJ; Szabo L Br J Pharmacol; 1998 Nov; 125(6):1258-66. PubMed ID: 9863655 [TBL] [Abstract][Full Text] [Related]
20. Neuroprotective effect of NMDA receptor glycine recognition site antagonism persists when brain temperature is controlled. Takaoka S; Bart RD; Pearlstein R; Brinkhous A; Warner DS J Cereb Blood Flow Metab; 1997 Feb; 17(2):161-7. PubMed ID: 9040495 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]