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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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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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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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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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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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Sodium channel modulators prevent oxygen and glucose deprivation injury and glutamate release in rat neocortical cultures

Neuropharmacology, 1997-08, Vol.36 (8), p.1031-1038

1997

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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 12626, a novel, competitive N-methyl-D-aspartate receptor antagonist

The Journal of pharmacology and experimental therapeutics, 1989-07, Vol.250 (1), p.100

1989

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NPC 16377, a potent and selective sigma-ligand. I. Receptor binding, neurochemical and neuroendocrine profile

The Journal of pharmacology and experimental therapeutics, 1993-05, Vol.265 (2), p.866

1993

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NPC 16377, a potent and selective sigma-ligand. II. Behavioral and neuroprotective profile

The Journal of pharmacology and experimental therapeutics, 1993-05, Vol.265 (2), p.876

1993

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Bridged .gamma.-carbolines and derivatives possessing selective and combined affinity for 5-HT2 and D2 receptors

Journal of medicinal chemistry, 1993-05, Vol.36 (10), p.1488-1495

1993

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4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol) Inhibits Peroxynitrite-Mediated Phenol Nitration

Chemical research in toxicology, 2000-04, Vol.13 (4), p.294-300

2000

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Partitioning a PPI Network into Overlapping Modules Constrained by High-Density and Periphery Tracking

ISRN biomathematics, 2012-05, Vol.2012 (2012), p.1-11

2012

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Scale Alpha and Beta of Quantitative Convergence and Chemical Reactivity Analysis in Dual Cholinesterase/Monoamine Oxidase Inhibitors for the Alzheimer Disease Treatment Using Density Functional Theory (DFT)

Journal of theoretical chemistry, 2013-12, Vol.2013 (2013), p.1-13

2013

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Effects of the calcium channel activator BAY-K-8644 on in vitro secretion of calcitonin and parathyroid hormone

Endocrinology (Philadelphia), 1986-02, Vol.118 (2), p.545-549

1986

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A Computational Determination of the Lowest Energy Electronic and Geometric States of First Row Transition Metal Dioxygen Dications

Journal of theoretical chemistry, 2013-09, Vol.2013 (2013), p.1-4

2013

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Secretion of Calcitonin Gene-Related Peptide from Baby Rat Thyroid Glands in Vitro

Experimental biology and medicine (Maywood, N.J.), 1985-12, Vol.180 (3), p.562-566

1985

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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 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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Rho‐associated kinase (ROCK) inhibitor, Y27632, promotes neurite outgrowth in PC12 cells in the absence of NGF

Journal of neurochemistry, 2002-06, Vol.81 (s1), p.92-92

2002

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

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

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

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

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

Sodium channel modulators prevent oxygen and glucose deprivation injury and glutamate release in rat neocortical cultures

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 12626, a novel, competitive N-methyl-D-aspartate receptor antagonist

NPC 16377, a potent and selective sigma-ligand. I. Receptor binding, neurochemical and neuroendocrine profile

NPC 16377, a potent and selective sigma-ligand. II. Behavioral and neuroprotective profile

Bridged .gamma.-carbolines and derivatives possessing selective and combined affinity for 5-HT2 and D2 receptors

4-Hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl (Tempol) Inhibits Peroxynitrite-Mediated Phenol Nitration

Partitioning a PPI Network into Overlapping Modules Constrained by High-Density and Periphery Tracking

Scale Alpha and Beta of Quantitative Convergence and Chemical Reactivity Analysis in Dual Cholinesterase/Monoamine Oxidase Inhibitors for the Alzheimer Disease Treatment Using Density Functional Theory (DFT)

Effects of the calcium channel activator BAY-K-8644 on in vitro secretion of calcitonin and parathyroid hormone

A Computational Determination of the Lowest Energy Electronic and Geometric States of First Row Transition Metal Dioxygen Dications

Secretion of Calcitonin Gene-Related Peptide from Baby Rat Thyroid Glands in Vitro

Inhibition of secretion of rat calcitonin by calmodulin inhibitors

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

Rho‐associated kinase (ROCK) inhibitor, Y27632, promotes neurite outgrowth in PC12 cells in the absence of NGF

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

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

Bradykinin as a pain mediator: receptors are localized to sensory neurons, and antagonists have analgesic actions

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