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Current Pharmaceutical Design|April 24, 1999
Antagonists selective for NMDA receptors containing the NR2B subunitB L Chenard, F S MennitiThe Journal of Pharmacology and Experimental Therapeutics|February 1, 1992
Neuroprotective effects of the N-methyl-D-aspartate receptor antagonists ifenprodil and SL-82,0715 on hippocampal cells in cultureI A Shalaby, B L Chenard, M A Prochniak, et al.Bioorganic & Medicinal Chemistry Letters|June 24, 2000
Methaqualone derivatives are potent noncompetitive AMPA receptor antagonistsB L Chenard, F S Menniti, M J Pagnozzi, et al.Neuropharmacology|April 13, 2000
CP-101,606, an NR2B subunit selective NMDA receptor antagonist, inhibits NMDA and injury induced c-fos expression and cortical spreading depression in rodentsF S Menniti, M J Pagnozzi, P Butler, et al.Journal of Medicinal Chemistry|May 18, 2001
Quinazolin-4-one alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor antagonists: structure-activity relationship of the C-2 side chain tetherB L Chenard, W M Welch, J F Blake, et al.Journal of Medicinal Chemistry|October 1, 1991
Separation of alpha 1 adrenergic and N-methyl-D-aspartate antagonist activity in a series of ifenprodil compoundsB L Chenard, I A Shalaby, B K Koe, et al.Neuropharmacology|January 24, 2002
Functional characterization of CP-465,022, a selective, noncompetitive AMPA receptor antagonistJ T Lazzaro, A V Paternain, J Lerma, et al.Journal of Medicinal Chemistry|March 1, 1990
A unified approach to systematic isosteric substitution for acidic groups and application to NMDA antagonists related to 2-amino-7-phosphonoheptanoateB L Chenard, C A Lipinski, B W Dominy, et al.Journal of Medicinal Chemistry|August 4, 1995
(1S,2S)-1-(4-hydroxyphenyl)-2-(4-hydroxy-4-phenylpiperidino)-1-propanol: a potent new neuroprotectant which blocks N-methyl-D-aspartate responsesB L Chenard, J Bordner, T W Butler, et al.Molecular Pharmacology|November 28, 2000
Characterization of the binding site for a novel class of noncompetitive alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptor antagonistsF S Menniti, B L Chenard, M B Collins, et al.Pageof 2