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A Selective Metabotropic Glutamate Receptor 7 Agonist: Activation of Receptor Signaling via an Allosteric Site Modulates Stress Parameters In vivo

Proceedings of the National Academy of Sciences - PNAS, 2005-12, Vol.102 (51), p.18712-18717

2005

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The selective nicotinic acetylcholine receptor α7 agonist JN403 is active in animal models of cognition, sensory gating, epilepsy and pain

Neuropharmacology, 2009-01, Vol.56 (1), p.254-263

2009

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Gamma-lactams—A novel scaffold for highly potent and selective α7 nicotinic acetylcholine receptor agonists

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (5), p.1287-1291

2009

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The selective nicotinic acetylcholine receptor alpha 7 agonist JN403 is active in animal models of cognition, sensory gating, epilepsy and pain

Neuropharmacology, 2009-01, Vol.56 (1), p.254-263

2009

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NGD 94-1 as an agonist at human recombinant dopamine D4.4 receptors expressed in HEK293 cells

European journal of pharmacology, 1999-05, Vol.372 (3), p.R9-R10

1999

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JN403, in vitro characterization of a novel nicotinic acetylcholine receptor α7 selective agonist

Neuroscience letters, 2007-04, Vol.416 (1), p.61-65

2007

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Effects of antalarmin, a CRF type 1 receptor antagonist, on anxiety-like behavior and motor activation in the rat

Brain research, 2002-10, Vol.952 (2), p.188-199

2002

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6-Amino quinazolinedione sulfonamides as orally active competitive AMPA receptor antagonists

Bioorganic & medicinal chemistry letters, 2012-01, Vol.22 (2), p.996-999

2012

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Gamma-lactams--a novel scaffold for highly potent and selective alpha 7 nicotinic acetylcholine receptor agonists

Bioorganic & medicinal chemistry letters, 2009-03, Vol.19 (5), p.1287-1291

2009

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Exploring subtype selectivity and metabolic stability of a novel series of ligands for the benzodiazepine binding site of the GABA A receptor

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (5), p.1523-1526

2011

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Exploring subtype selectivity and metabolic stability of a novel series of ligands for the benzodiazepine binding site of the GABAA receptor

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (5), p.1523-1526

2011

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Coupling of human nicotinic acetylcholine receptors α7 to calcium channels in GH3 cells

Neuropharmacology, 2005, Vol.48 (2), p.215-227

2005

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Toward Selective ERβ Agonists for Central Nervous System Disorders: Synthesis and Characterization of Aryl Benzthiophenes

Journal of medicinal chemistry, 2002-03, Vol.45 (7), p.1399-1401

2002

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Coupling of human nicotinic acetylcholine receptors alpha 7 to calcium channels in GH3 cells

Neuropharmacology, 2005-02, Vol.48 (2), p.215-227

2005

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Exploring subtype selectivity and metabolic stability of a novel series of ligands for the benzodiazepine binding site of the GABA sub(A receptor)

Bioorganic & medicinal chemistry letters, 2011-03, Vol.21 (5), p.1523-1526

2011

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JN403, in vitro characterization of a novel nicotinic acetylcholine receptor alpha7 selective agonist

Neuroscience letters, 2007-04, Vol.416 (1), p.61-65

2007

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Study of the calcium dynamics of the human α4β2, α3β4 and α1β1γδ nicotinic acetylcholine receptors

Naunyn-Schmiedeberg's archives of pharmacology, 2002-09, Vol.366 (3), p.235-245

2002

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The selective nicotinic acetylcholine receptor alpha7 agonist JN403 is active in animal models of cognition, sensory gating, epilepsy and pain

Neuropharmacology, 2009-01, Vol.56 (1), p.254-263

2009

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NGD 94-1 as an agonist at human recombinant dopamine D 4.4 receptors expressed in HEK293 cells

European journal of pharmacology, 1999-05, Vol.372 (3), p.R9-R10

1999

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Labeling strategies of selected subtypes of the hexahydronaphth[2,3-b]-1,4-oxazine- and octahydrobenzo[g]quinoline-type

Journal of labelled compounds & radiopharmaceuticals, 2007-04, Vol.50 (5-6), p.616-619

2007

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Toward selective ERbeta agonists for central nervous system disorders: synthesis and characterization of aryl benzthiophenes

Journal of medicinal chemistry, 2002-03, Vol.45 (7), p.1399-1401

2002

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Study of the calcium dynamics of the human alpha4beta2, alpha3beta4 and alpha1beta1gammadelta nicotinic acetylcholine receptors

Naunyn-Schmiedeberg's archives of pharmacology, 2002-09, Vol.366 (3), p.235-245

2002

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Cataleptogenic effect of subtype selective 5-HT receptor antagonists in the rat

European journal of pharmacology, 1998-02, Vol.343 (2), p.201-207

1998

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Labeling strategies of selected subtypes of the hexahydro-naphth[2,3-b]-1,4-oxazine-and octahydrobenzo[g ]quinoline-type

Journal of labelled compounds & radiopharmaceuticals, 2007, Vol.50 (5-6), p.616-619

2007

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5-HT1D binding sites in various species: similar pharmacological profile in dog, monkey, calf, guinea-pig and human brain membranes

Naunyn-Schmiedeberg's archives of pharmacology, 1992-09, Vol.346 (3), p.243-248

1992

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A Selective Metabotropic Glutamate Receptor 7 Agonist: Activation of Receptor Signaling via an Allosteric Site Modulates Stress Parameters In vivo

The selective nicotinic acetylcholine receptor α7 agonist JN403 is active in animal models of cognition, sensory gating, epilepsy and pain

Gamma-lactams—A novel scaffold for highly potent and selective α7 nicotinic acetylcholine receptor agonists

The selective nicotinic acetylcholine receptor alpha 7 agonist JN403 is active in animal models of cognition, sensory gating, epilepsy and pain

NGD 94-1 as an agonist at human recombinant dopamine D4.4 receptors expressed in HEK293 cells

JN403, in vitro characterization of a novel nicotinic acetylcholine receptor α7 selective agonist

Effects of antalarmin, a CRF type 1 receptor antagonist, on anxiety-like behavior and motor activation in the rat

6-Amino quinazolinedione sulfonamides as orally active competitive AMPA receptor antagonists

Gamma-lactams--a novel scaffold for highly potent and selective alpha 7 nicotinic acetylcholine receptor agonists

Exploring subtype selectivity and metabolic stability of a novel series of ligands for the benzodiazepine binding site of the GABA A receptor

Exploring subtype selectivity and metabolic stability of a novel series of ligands for the benzodiazepine binding site of the GABAA receptor

Coupling of human nicotinic acetylcholine receptors α7 to calcium channels in GH3 cells

Toward Selective ERβ Agonists for Central Nervous System Disorders: Synthesis and Characterization of Aryl Benzthiophenes

Coupling of human nicotinic acetylcholine receptors alpha 7 to calcium channels in GH3 cells

Exploring subtype selectivity and metabolic stability of a novel series of ligands for the benzodiazepine binding site of the GABA sub(A receptor)

JN403, in vitro characterization of a novel nicotinic acetylcholine receptor alpha7 selective agonist

Study of the calcium dynamics of the human α4β2, α3β4 and α1β1γδ nicotinic acetylcholine receptors

The selective nicotinic acetylcholine receptor alpha7 agonist JN403 is active in animal models of cognition, sensory gating, epilepsy and pain

NGD 94-1 as an agonist at human recombinant dopamine D 4.4 receptors expressed in HEK293 cells

Labeling strategies of selected subtypes of the hexahydronaphth[2,3-b]-1,4-oxazine- and octahydrobenzo[g]quinoline-type

Toward selective ERbeta agonists for central nervous system disorders: synthesis and characterization of aryl benzthiophenes

Study of the calcium dynamics of the human alpha4beta2, alpha3beta4 and alpha1beta1gammadelta nicotinic acetylcholine receptors

Cataleptogenic effect of subtype selective 5-HT receptor antagonists in the rat

Labeling strategies of selected subtypes of the hexahydro-naphth[2,3-b]-1,4-oxazine-and octahydrobenzo[g ]quinoline-type

5-HT1D binding sites in various species: similar pharmacological profile in dog, monkey, calf, guinea-pig and human brain membranes

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