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Comparative Effects of LY3020371, a Potent and Selective Metabotropic Glutamate (mGlu) 2/3 Receptor Antagonist, and Ketamine, a Noncompetitive N -Methyl-d-Aspartate Receptor Antagonist in Rodents: Evidence Supporting the Use of mGlu2/3 Antagonists, for the Treatment of Depression

The Journal of pharmacology and experimental therapeutics, 2017-04, Vol.361 (1), p.68-86

2017

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LY354740 is a potent and highly selective group II metabotropic glutamate receptor agonist in cells expressing human glutamate receptors

Neuropharmacology, 1997, Vol.36 (1), p.1-11

1997

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The bacterial quorum sensing molecule, 2-heptyl-3-hydroxy-4-quinolone (PQS), inhibits signal transduction mechanisms in brain tissue and is behaviorally active in mice

Pharmacological research, 2021-08, Vol.170, p.105691-105691, Article 105691

2021

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Selective inhibition of forskolin-stimulated cyclic AMP formation in rat hippocampus by a novel mGluR agonist, 2R,4R-4-aminopyrrolidine-2,4- dicarboxylate

Neuropharmacology, 1995-08, Vol.34 (8), p.843-850

1995

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Blockade of N-methyl-D-aspartate induced convulsions by 1-aminocyclopropanecarboxylates

Life sciences (1973), 1989, Vol.45 (18), p.1647-1655

1989

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LY354740: a metabotropic glutamate receptor agonist which ameliorates symptoms of nicotine withdrawal in rats

Neuropharmacology, 1997-11, Vol.36 (11), p.1511-1516

1997

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The Novel Metabotropic Glutamate Receptor Agonist 2 R ,4 R -APDC Potentiates Stimulation of Phosphoinositide Hydrolysis in the Rat Hippocampus by 3,5-dihydroxyphenylglycine: Evidence for a Synergistic Interaction Between Group 1 and Group 2 Receptors

Neuropharmacology, 1996-12, Vol.35 (12), p.1661-1672

1996

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Tolerance to the motor impairment, but not to the reversal of PCP-induced motor activities by oral administration of the mGlu2/3 receptor agonist, LY379268

Naunyn-Schmiedeberg's archives of pharmacology, 2000-01, Vol.361 (1), p.39-46

2000

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1-BCP, a memory-enhancing agent, selectively potentiates AMPA-induced [ 3H]norepinephrine release in rat hippocampal slices

Neuropharmacology, 1995-02, Vol.34 (2), p.141-147

1995

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Presynaptic modulation of excitatory amino acid release: An in vivo microdialysis study

Neuropharmacology, 1996-06, Vol.35 (6), p.A2-A2

1996

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Development of metabotropic glutamate receptor subtype selective drugs

European neuropsychopharmacology, 1999-09, Vol.9, p.204-205

1999

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Agonists and antagonists of metabotropic glutamate receptor subtypes as anticonvulsant agents

Neuropharmacology, 1996-06, Vol.35 (6), p.A31-A31

1996

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Selective inhibition of forskolin-stimulated cyclic AMP formation in rat hippocampus by a novel mGluR agonist, 2 R,4 R-4-aminopyrrolidine-2,4-dicarboxylate

Neuropharmacology, 1995, Vol.34 (8), p.843-850

1995

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A bridgehead α-amino carbanion: facile preparation of C5(bridgehead)-substituted analogues of (±)-5H-dibenzo[a,d]cyclohepten-5,10-imine including a stable α-iodo secondary amine

Tetrahedron letters, 1989, Vol.30 (8), p.911-914

1989

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Discovery of LY314582 and its (+) enantiomer, LY354740: Highly potent and selective group 2 metabotropic glutamate receptor agonists

Neuropharmacology, 1996-06, Vol.35 (6), p.A21-A21

1996

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Specificity of phencyclidine-like drugs and benzomorphan opiates for two high affinity phencyclidine binding sites in guinea pig brain

Neuropharmacology, 1990-09, Vol.29 (9), p.811-817

1990

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Pseudoallosteric modulation by (+)-MK801 of NMDA-coupled phencyclidine binding sites

Life sciences (1973), 1990, Vol.47 (16), p.PL77-PL82

1990

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Wash-resistant inhibition of phencyclidine- and haloperidol-sensitive sigma receptor sites in guinea pig brain by putative affinity ligands: Determination of selectivity

Neuropharmacology, 1990-11, Vol.29 (11), p.1047-1053

1990

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Comparative Effects of LY3020371, a Potent and Selective Metabotropic Glutamate (mGlu) 2/3 Receptor Antagonist, and Ketamine, a Noncompetitive N -Methyl-d-Aspartate Receptor Antagonist in Rodents: Evidence Supporting the Use of mGlu2/3 Antagonists, for the Treatment of Depression

LY354740 is a potent and highly selective group II metabotropic glutamate receptor agonist in cells expressing human glutamate receptors

The bacterial quorum sensing molecule, 2-heptyl-3-hydroxy-4-quinolone (PQS), inhibits signal transduction mechanisms in brain tissue and is behaviorally active in mice

Selective inhibition of forskolin-stimulated cyclic AMP formation in rat hippocampus by a novel mGluR agonist, 2R,4R-4-aminopyrrolidine-2,4- dicarboxylate

Blockade of N-methyl-D-aspartate induced convulsions by 1-aminocyclopropanecarboxylates

LY354740: a metabotropic glutamate receptor agonist which ameliorates symptoms of nicotine withdrawal in rats

The Novel Metabotropic Glutamate Receptor Agonist 2 R ,4 R -APDC Potentiates Stimulation of Phosphoinositide Hydrolysis in the Rat Hippocampus by 3,5-dihydroxyphenylglycine: Evidence for a Synergistic Interaction Between Group 1 and Group 2 Receptors

Tolerance to the motor impairment, but not to the reversal of PCP-induced motor activities by oral administration of the mGlu2/3 receptor agonist, LY379268

1-BCP, a memory-enhancing agent, selectively potentiates AMPA-induced [ 3H]norepinephrine release in rat hippocampal slices

Presynaptic modulation of excitatory amino acid release: An in vivo microdialysis study

Development of metabotropic glutamate receptor subtype selective drugs

Agonists and antagonists of metabotropic glutamate receptor subtypes as anticonvulsant agents

Selective inhibition of forskolin-stimulated cyclic AMP formation in rat hippocampus by a novel mGluR agonist, 2 R,4 R-4-aminopyrrolidine-2,4-dicarboxylate

A bridgehead α-amino carbanion: facile preparation of C5(bridgehead)-substituted analogues of (±)-5H-dibenzo[a,d]cyclohepten-5,10-imine including a stable α-iodo secondary amine

Discovery of LY314582 and its (+) enantiomer, LY354740: Highly potent and selective group 2 metabotropic glutamate receptor agonists

Specificity of phencyclidine-like drugs and benzomorphan opiates for two high affinity phencyclidine binding sites in guinea pig brain

Pseudoallosteric modulation by (+)-MK801 of NMDA-coupled phencyclidine binding sites

Wash-resistant inhibition of phencyclidine- and haloperidol-sensitive sigma receptor sites in guinea pig brain by putative affinity ligands: Determination of selectivity

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