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Inhibition of K +-evoked glutamate release from rat neocortical and hippocampal slices by gabapentin

Neuroscience letters, 2000-02, Vol.280 (2), p.107-110

2000

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A specific inhibitor of calcium/calmodulin-dependent protein kinase-II provides neuroprotection against NMDA- and hypoxia/hypoglycemia-induced cell death

The Journal of neuroscience, 1995-05, Vol.15 (5), p.4093-4101

1995

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Bradykinin as a Pain Mediator: Receptors are Localized to Sensory Neurons, and Antagonists Have Analgesic Actions

Proceedings of the National Academy of Sciences - PNAS, 1988-05, Vol.85 (9), p.3245-3249

1988

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Synthesis of 1,4,7,8,9,10-hexahydro-9-methyl-6-nitropyrido[3,4-f]-quinoxaline-2,3-dione and related quinoxalinediones: characterization of .alpha.-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (and N-methyl-D-aspartate) receptor and anticonvulsant activity

Journal of medicinal chemistry, 1995-09, Vol.38 (19), p.3720-3740

1995

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Dextromethorphan inhibits NMDA-induced convulsions

European journal of pharmacology, 1988-06, Vol.151 (1), p.151-154

1988

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Inhibition of K super(+)-evoked glutamate release from rat neocortical and hippocampal slices by gabapentin

Neuroscience letters, 2000-02, Vol.280 (2), p.107-110

2000

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Potent, Orally Active, Competitive N-Methyl-D-aspartate (NMDA) Receptor Antagonists Are Substrates for a Neutral Amino Acid Uptake System in Chinese Hamster Ovary Cells

Journal of medicinal chemistry, 1995-05, Vol.38 (11), p.1955-1965

1995

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Possible cerebroprotective and in vivo NMDA antagonist activities of sigma agents

Brain research bulletin, 1991-03, Vol.26 (3), p.461-465

1991

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Pharmacological profile of NPC 17742 [2R,4R,5S-(2-amino-4,5-(1, 2-cyclohexyl)-7-phosphonoheptanoic acid)], a potent, selective and competitive N-methyl-D-aspartate receptor antagonist

The Journal of pharmacology and experimental therapeutics, 1993-01, Vol.264 (1), p.256

1993

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A specific inhibitor of calcium/calmodulin-dependent protein kinase-II provides neuroprotection against NMDA- and hypoxia/hypoglycemia-induced cell death

The Journal of neuroscience, 1995-01, Vol.15 (5), p.art II

1995

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Synthesis and glutamate antagonist activity of 4-phosphonoalkylquinoline derivatives: A novel class of non-NMDA antagonist

Bioorganic & medicinal chemistry letters, 1994-08, Vol.4 (16), p.2035-2040

1994

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Pharmacology of (2 R, 4 R, 5 S)-2-amino-4,5-(1,2-cyclohexyl)-7-phosphonoheptanoic acid (NPC 17742); a selective, systemically active, competitive NMDA antagonist

Bioorganic & medicinal chemistry letters, 1993, Vol.3 (1), p.33-38

1993

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Phosphonoethylphenylalanine derivatives as novel antagonists of non-NMDA ionotropic glutamate receptors

Bioorganic & medicinal chemistry letters, 1992-10, Vol.2 (10), p.1269-1274

1992

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Inhibition of secretion of rat calcitonin by calmodulin inhibitors

Calcified tissue international, 1986-02, Vol.38 (2), p.103-108

1986

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Synthesis of 1,4,7,8,9,10-hexahydro-9-methyl 6-nitropyrido[3,4-fl-quinoxaline-2,3-dione and related quinoxalinediones: Characterization of alpha -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (and N-methyl-D-aspartate) receptor and anticonvulsant activity

Journal of medicinal chemistry, 1995-01, Vol.38 (19), p.3720-3740

1995

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Inhibition of K +-evoked glutamate release from rat neocortical and hippocampal slices by gabapentin

A specific inhibitor of calcium/calmodulin-dependent protein kinase-II provides neuroprotection against NMDA- and hypoxia/hypoglycemia-induced cell death

Bradykinin as a Pain Mediator: Receptors are Localized to Sensory Neurons, and Antagonists Have Analgesic Actions

Synthesis of 1,4,7,8,9,10-hexahydro-9-methyl-6-nitropyrido[3,4-f]-quinoxaline-2,3-dione and related quinoxalinediones: characterization of .alpha.-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (and N-methyl-D-aspartate) receptor and anticonvulsant activity

Dextromethorphan inhibits NMDA-induced convulsions

Inhibition of K super(+)-evoked glutamate release from rat neocortical and hippocampal slices by gabapentin

Potent, Orally Active, Competitive N-Methyl-D-aspartate (NMDA) Receptor Antagonists Are Substrates for a Neutral Amino Acid Uptake System in Chinese Hamster Ovary Cells

Possible cerebroprotective and in vivo NMDA antagonist activities of sigma agents

Pharmacological profile of NPC 17742 [2R,4R,5S-(2-amino-4,5-(1, 2-cyclohexyl)-7-phosphonoheptanoic acid)], a potent, selective and competitive N-methyl-D-aspartate receptor antagonist

A specific inhibitor of calcium/calmodulin-dependent protein kinase-II provides neuroprotection against NMDA- and hypoxia/hypoglycemia-induced cell death

Synthesis and glutamate antagonist activity of 4-phosphonoalkylquinoline derivatives: A novel class of non-NMDA antagonist

Pharmacology of (2 R, 4 R, 5 S)-2-amino-4,5-(1,2-cyclohexyl)-7-phosphonoheptanoic acid (NPC 17742); a selective, systemically active, competitive NMDA antagonist

Phosphonoethylphenylalanine derivatives as novel antagonists of non-NMDA ionotropic glutamate receptors

Inhibition of secretion of rat calcitonin by calmodulin inhibitors

Synthesis of 1,4,7,8,9,10-hexahydro-9-methyl 6-nitropyrido[3,4-fl-quinoxaline-2,3-dione and related quinoxalinediones: Characterization of alpha -amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (and N-methyl-D-aspartate) receptor and anticonvulsant activity

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