van den Bos R, Charria Ortiz G, Cools A (1992). „Injections of the NMDA-antagonist D-2-amino-7-phosphonoheptanoic acid (AP-7) into the nucleus accumbens of rats enhance switching between cue-directed behaviours in a swimming test procedure”. Behav Brain Res48 (2): 165–70. DOI:10.1016/S0166-4328(05)80153-6. PMID1535501.
Eblen F, Löschmann P, Wüllner U, Turski L, Klockgether T (1996). „Effects of 7-nitroindazole, NG-nitro-L-arginine, and D-CPPene on harmaline-induced postural tremor, N-methyl-D-aspartate-induced seizures, and lisuride-induced rotations in rats with nigral 6-hydroxydopamine lesions”. Eur J Pharmacol299 (1–3): 9–16. DOI:10.1016/0014-2999(95)00795-4. PMID8901001.
Wong BY, Coulter DA, Choi DW, Prince DA (1988). „Dextrorphan and dextromethorphan, common antitussives, are antiepileptic and antagonize N-methyl-D-aspartate in brain slices”. Neurosci. Lett.85 (2): 261–6. DOI:10.1016/0304-3940(88)90362-X. PMID2897648.
Fix AS, Horn JW, Wightman KA, et al. (1993). „Neuronal vacuolization and necrosis induced by the noncompetitive N-methyl-D-aspartate (NMDA) antagonist MK(+)801 (dizocilpine maleate): a light and electron microscopic evaluation of the rat retrosplenial cortex”. Exp. Neurol.123 (2): 204–15. DOI:10.1006/exnr.1993.1153. PMID8405286.
van den Bos R, Charria Ortiz G, Cools A (1992). „Injections of the NMDA-antagonist D-2-amino-7-phosphonoheptanoic acid (AP-7) into the nucleus accumbens of rats enhance switching between cue-directed behaviours in a swimming test procedure”. Behav Brain Res48 (2): 165–70. DOI:10.1016/S0166-4328(05)80153-6. PMID1535501.
Eblen F, Löschmann P, Wüllner U, Turski L, Klockgether T (1996). „Effects of 7-nitroindazole, NG-nitro-L-arginine, and D-CPPene on harmaline-induced postural tremor, N-methyl-D-aspartate-induced seizures, and lisuride-induced rotations in rats with nigral 6-hydroxydopamine lesions”. Eur J Pharmacol299 (1–3): 9–16. DOI:10.1016/0014-2999(95)00795-4. PMID8901001.
Wong BY, Coulter DA, Choi DW, Prince DA (1988). „Dextrorphan and dextromethorphan, common antitussives, are antiepileptic and antagonize N-methyl-D-aspartate in brain slices”. Neurosci. Lett.85 (2): 261–6. DOI:10.1016/0304-3940(88)90362-X. PMID2897648.
Fix AS, Horn JW, Wightman KA, et al. (1993). „Neuronal vacuolization and necrosis induced by the noncompetitive N-methyl-D-aspartate (NMDA) antagonist MK(+)801 (dizocilpine maleate): a light and electron microscopic evaluation of the rat retrosplenial cortex”. Exp. Neurol.123 (2): 204–15. DOI:10.1006/exnr.1993.1153. PMID8405286.
Chawla, PS; Kochar MS (2006). „What's new in clinical pharmacology and therapeutics”. WMJ105 (3): 24–29. PMID16749321.
Grasshoff C, Drexler B, Rudolph U, Antkowiak B (2006). „Anaesthetic drugs: linking molecular actions to clinical effects”. Curr. Pharm. Des.12 (28): 3665–79. DOI:10.2174/138161206778522038. PMID17073666.
Ko JC, Smith TA, Kuo WC, Nicklin CF (1998). „Comparison of anesthetic and cardiorespiratory effects of diazepam-butorphanol-ketamine, acepromazine-butorphanol-ketamine, and xylazine-butorphanol-ketamine in ferrets”. Journal of the American Animal Hospital Association34 (5): 407–16. PMID9728472.
Banerjee A, Schepmann D, Köhler J, Würthwein EU, Wünsch B (November 2010). „Synthesis and SAR studies of chiral non-racemic dexoxadrol analogues as uncompetitive NMDA receptor antagonists”. Bioorg. Med. Chem.18 (22): 7855–67. DOI:10.1016/j.bmc.2010.09.047. PMID20965735.
Nadler V, Mechoulam R, Sokolovsky M (November 1993). „The non-psychotropic cannabinoid (+)-(3S,4S)-7-hydroxy-delta 6- tetrahydrocannabinol 1,1-dimethylheptyl (HU-211) attenuates N-methyl-D-aspartate receptor-mediated neurotoxicity in primary cultures of rat forebrain”. Neurosci. Lett.162 (1–2): 43–5. DOI:10.1016/0304-3940(93)90555-Y. PMID8121633.
Muir, KW (2005). „Glutamate-based therapeutic approaches: clinical trials with NMDA antagonists”. Current Opinion in Pharmacology6 (1): 53–60. DOI:10.1016/j.coph.2005.12.002. PMID16359918.
Kvist, T; et al.. „Crystal structure and pharmacological characterization of a novel N-methyl-D-aspartate (NMDA) receptor antagonist at the GluN1 glycine binding site.”. J Biol Chem. (2013). PMID24072709.