ANIMAL EXPERIMENT;
ARTICLE;
CONTROLLED STUDY;
DRUG ACTIVITY;
DRUG DESIGN;
DRUG POTENCY;
DRUG SOLUBILITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
INTRAVENOUS DRUG ADMINISTRATION;
MALE;
MOUSE;
NONHUMAN;
RECEPTOR AFFINITY;
STEREOCHEMISTRY;
STRUCTURE ACTIVITY RELATION;
The excitatory amino acid receptors: Their classes, pharmacology and distinct properties in the function of the central nervous system
Monoghan, D. T.; Bridges, R. D.; Cotman, C. W. The excitatory amino acid receptors: their classes, pharmacology and distinct properties in the function of the central nervous system. Annu. Rev. Pharmacol. Toxicol. 1990, 29, 365-402.
AMPA receptor agonists, antagonists and modulators: Their potential for clinical utility
Bigge, C. F.; Nikam, S. S. AMPA receptor agonists, antagonists and modulators: their potential for clinical utility. Exp. Opin. Ther. Patents 1997, 7, 1099-1114.
2,3-Dihydroxy-6-nitro-7-sulfamoylbenzo[f]quinoxaline: A neuroprotectant for cerebral ischemia
Sheardown, M. J.; Nielson, E. O.; Hanson, A. J.; Jacobsen, P.; Honore, T. 2,3-Dihydroxy-6-nitro-7-sulfamoylbenzo[f]quinoxaline: a neuroprotectant for cerebral ischemia. Science 1990, 247, 571-574.
NS 257 1,2,3,6,7,8-hexahydro-3-(hydroxyimino)-N,N,7-trimethyl-2-oxobenzo[2,1-b:3,4- c′]dipyrrole-5-sulfonamide is a potent, systemically active AMPA receptor antagonist
Watjen, F.; Bigge, C. F.; Jensen, L. H.; Boxer, P. A.; Lescosky, L. J.; Nielsen, E. O.; Malone, T. C.; Campbell, G. W.; Coughenour, L. L.; Rock, D. M.; Drejer, J.; Marcoux, F. W. NS 257 (1,2,3,6,7,8-hexahydro-3-(hydroxyimino)-N,N,7-trimethyl-2-oxobenzo[2,1-b:3,4- c′]dipyrrole-5-sulfonamide is a potent, systemically active AMPA receptor antagonist. Bioorg. Med. Chem. Lett. 1994, 4, 371-376.
Bigge, C. F.; Malone, T. C.; Boxer, P. A.; Nelson, C. B.; Ortwine, D. F.; Schelkun, R. M.; Retz, D. M.; Lescosky, L. J.; Borosky, S. A.; Vartanian, M. G.; Schwarz, R. D.; Campbell, G. W.; Robichaud, L. J.; Watjen, F. J. Med. Chem. 1995, 38, 3720-3740.
Delayed treatment with the novel AMPA receptor antagonist PD152247 (PNQX), reduces lesion size following focal ischemia and reperfusion in the rat
Schielke, G. P.; Kupina, N. C.; Boxer, P. A.; Cordon, J. J.; Bigge, C. F.; Marcoux, F. W. Delayed treatment with the novel AMPA receptor antagonist PD152247 (PNQX), reduces lesion size following focal ischemia and reperfusion in the rat. J. Cereb. Blood Flow Metab. 1995, 15 (Suppl. 1), S372.
Thiocyanate stabilizes AMPA receptor binding to the quisqualate receptor
Nielson, E. O.; Cha, J. J.; Honore, T.; Penny, J. B.; Young, A. B. Thiocyanate stabilizes AMPA receptor binding to the quisqualate receptor. Eur. J. Pharmacol. 1988, 157, 197-203.
Thiocyanate stabilizes AMPA receptor binding to the quisqualate receptor
Nielson, E. O.; Cha, J. J.; Honore, T.; Penny, J. B.; Young, A. B. Thiocyanate stabilizes AMPA receptor binding to the quisqualate receptor. Eur. J. Pharmacol. 1988, 157, 197-203.
A novel non-NMDA receptor antagonist shows selective displacement of low-affinity [3H]kainate binding
Johansen, T. H.; Drejer, J.; Watjen, F.; Nielsen, E. O. A novel non-NMDA receptor antagonist shows selective displacement of low-affinity [3H]kainate binding. Eur. J. Pharmacol. 1993, 246, 195-204.
Characterization of the binding of radioligands to the NMDA, phencyclidine, and glycine receptors in buffy coat membranes
Jones, S. M.; Snell, L. D.; Johnson, K. M. Characterization of the binding of radioligands to the NMDA, phencyclidine, and glycine receptors in buffy coat membranes. J. Pharmacol. Methods 1989, 21, 161-168.
Antiepileptic drug development: II. Anticonvulsant drug screening
Krall, R. L.; Penry, J. K.; White, B. G.; Kupferberg, H. J.; Swinyard, E. A. Antiepileptic drug development: II. Anticonvulsant drug screening. Epilepsia 1978, 19, 409-428.