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Augmentation of cognitive function by NS9283, a stoichiometry‐dependent positive allosteric modulator of α2‐ and α4‐containing nicotinic acetylcholine receptors

British journal of pharmacology, 2012-09, Vol.167 (1), p.164-182

2012

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Comparison of the novel subtype-selective GABAA receptor-positive allosteric modulator NS11394 [3'-[5-(1-hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile] with diazepam, zolpidem, bretazenil, and gaboxadol in rat models of inflammatory and neuropathic pain

The Journal of pharmacology and experimental therapeutics, 2008-12, Vol.327 (3), p.969

2008

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NS11394 [3'-[5-(1-hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile], a unique subtype-selective GABAA receptor positive allosteric modulator: in vitro actions, pharmacokinetic properties and in vivo anxiolytic efficacy

The Journal of pharmacology and experimental therapeutics, 2008-12, Vol.327 (3), p.954

2008

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Anxiolytic effects of Maxipost (BMS-204352) and retigabine via activation of neuronal Kv7 channels

The Journal of pharmacology and experimental therapeutics, 2005-07, Vol.314 (1), p.282

2005

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Unravelling the mechanism of action of NS9283, a positive allosteric modulator of (α4)3(β2)2 nicotinic ACh receptors

British journal of pharmacology, 2013-04, Vol.168 (8), p.2000-2010

2013

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Augmentation of cognitive function by NS9283, a stoichiometry-dependent positive allosteric modulator of alpha 2- and alpha 4-containing nicotinic acetylcholine receptors

British journal of pharmacology, 2012-09, Vol.167 (1), p.164-182

2012

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A pharmacological characterization of GABA, THIP and DS2 at binary α4β3 and β3δ receptors: GABA activates β3δ receptors via the β3(+)δ(-) interface

Brain research, 2016-08, Vol.1644, p.222-230

2016

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GABAA α5 subunit-containing receptors do not contribute to reversal of inflammatory-induced spinal sensitization as indicated by the unique selectivity profile of the GABAA receptor allosteric modulator NS16085

Biochemical pharmacology, 2015-02, Vol.93 (3), p.370-379

2015

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pH Dependency and Desensitization Kinetics of Heterologously Expressed Combinations of Acid-sensing Ion Channel Subunits

The Journal of biological chemistry, 2004-03, Vol.279 (12), p.11006-11015

2004

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Unraveling the high- and low-sensitivity agonist responses of nicotinic acetylcholine receptors

The Journal of neuroscience, 2011-07, Vol.31 (30), p.10759-10766

2011

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Pharmacological characterization of small‐conductance Ca2+‐activated K+ channels stably expressed in HEK 293 cells

British journal of pharmacology, 2000-03, Vol.129 (5), p.991-999

2000

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Characterization of the cloned human intermediate-conductance Ca2+-activated K+ channel

American Journal of Physiology: Cell Physiology, 1998-09, Vol.275 (3), p.C848

1998

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Cloning, expression, and distribution of a Ca(2+)-activated K+ channel beta-subunit from human brain

Proceedings of the National Academy of Sciences - PNAS, 1996-08, Vol.93 (17), p.9200-9205

1996

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Comparison of the Novel Subtype-Selective GABA A Receptor-Positive Allosteric Modulator NS11394 [3′-[5-(1-Hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile] with Diazepam, Zolpidem, Bretazenil, and Gaboxadol in Rat Models of Inflammatory and Neuropathic Pain

The Journal of pharmacology and experimental therapeutics, 2008-12, Vol.327 (3), p.969-981

2008

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A pharmacological characterization of GABA, THIP and DS2 at binary alpha 4 beta 3 and beta 3 delta receptors: GABA activates beta 3 delta receptors via the beta 3(+) delta (-) interface

Brain research, 2016-08, Vol.1644, p.222-230

2016

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NS11394 [3′-[5-(1-Hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile], a Unique Subtype-Selective GABA A Receptor Positive Allosteric Modulator: In Vitro Actions, Pharmacokinetic Properties and in Vivo Anxiolytic Efficacy

The Journal of pharmacology and experimental therapeutics, 2008-12, Vol.327 (3), p.954-968

2008

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Distinct Structural Features of Cyclothiazide Are Responsible for Effects on Peak Current Amplitude and Desensitization Kinetics at iGluR2

Journal of molecular biology, 2009-09, Vol.391 (5), p.906-917

2009

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Stable expression of the human large‐conductance Ca2+‐activated K+ channel α‐ and β‐subunits in HEK293 cells

FEBS letters, 1997-09, Vol.415 (1), p.67-70

1997

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Identification of a novel voltage-gated Na+ channel rNa(v)1.5a in the rat hippocampal progenitor stem cell line HiB5

Pflügers Archiv, 2001-10, Vol.443 (1), p.18

2001

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Pharmacological characterization of small-conductance Ca(2+)-activated K(+) channels stably expressed in HEK 293 cells

British journal of pharmacology, 2000-03, Vol.129 (5), p.991-999

2000

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GABA sub(A) alpha 5 subunit-containing receptors do not contribute to reversal of inflammatory-induced spinal sensitization as indicated by the unique selectivity profile of the GABA sub(A) receptor allosteric modulator NS16085

Biochemical pharmacology, 2015-02, Vol.93 (3), p.370-379

2015

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Modulation of the Ca2+-dependent K+ channel, hslo, by the substituted diphenylurea NS 1608, paxilline and internal Ca2

Neuropharmacology, 1996, Vol.35 (7), p.903-914

1996

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Activation of human IK and SK Ca2+ -activated K+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime)

Biochimica et biophysica acta, 2004-10, Vol.1665 (1-2), p.1-5

2004

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A Mosaic of Functional Kainate Receptors in Hippocampal Interneurons

The Journal of neuroscience, 2004-10, Vol.24 (41), p.8986-8993

2004

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Screening for lead compounds for Alzheimer's disease with dual mode of action, mimicking galanthamine at the human nicotinic receptors

Planta medica, 2016, Vol.81 (S 01), p.S1-S381

2016

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Augmentation of cognitive function by NS9283, a stoichiometry‐dependent positive allosteric modulator of α2‐ and α4‐containing nicotinic acetylcholine receptors

Comparison of the novel subtype-selective GABAA receptor-positive allosteric modulator NS11394 [3'-[5-(1-hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile] with diazepam, zolpidem, bretazenil, and gaboxadol in rat models of inflammatory and neuropathic pain

NS11394 [3'-[5-(1-hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile], a unique subtype-selective GABAA receptor positive allosteric modulator: in vitro actions, pharmacokinetic properties and in vivo anxiolytic efficacy

Anxiolytic effects of Maxipost (BMS-204352) and retigabine via activation of neuronal Kv7 channels

Unravelling the mechanism of action of NS9283, a positive allosteric modulator of (α4)3(β2)2 nicotinic ACh receptors

Augmentation of cognitive function by NS9283, a stoichiometry-dependent positive allosteric modulator of alpha 2- and alpha 4-containing nicotinic acetylcholine receptors

A pharmacological characterization of GABA, THIP and DS2 at binary α4β3 and β3δ receptors: GABA activates β3δ receptors via the β3(+)δ(-) interface

GABAA α5 subunit-containing receptors do not contribute to reversal of inflammatory-induced spinal sensitization as indicated by the unique selectivity profile of the GABAA receptor allosteric modulator NS16085

pH Dependency and Desensitization Kinetics of Heterologously Expressed Combinations of Acid-sensing Ion Channel Subunits

Unraveling the high- and low-sensitivity agonist responses of nicotinic acetylcholine receptors

Pharmacological characterization of small‐conductance Ca2+‐activated K+ channels stably expressed in HEK 293 cells

Characterization of the cloned human intermediate-conductance Ca2+-activated K+ channel

Cloning, expression, and distribution of a Ca(2+)-activated K+ channel beta-subunit from human brain

Comparison of the Novel Subtype-Selective GABA A Receptor-Positive Allosteric Modulator NS11394 [3′-[5-(1-Hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile] with Diazepam, Zolpidem, Bretazenil, and Gaboxadol in Rat Models of Inflammatory and Neuropathic Pain

A pharmacological characterization of GABA, THIP and DS2 at binary alpha 4 beta 3 and beta 3 delta receptors: GABA activates beta 3 delta receptors via the beta 3(+) delta (-) interface

NS11394 [3′-[5-(1-Hydroxy-1-methyl-ethyl)-benzoimidazol-1-yl]-biphenyl-2-carbonitrile], a Unique Subtype-Selective GABA A Receptor Positive Allosteric Modulator: In Vitro Actions, Pharmacokinetic Properties and in Vivo Anxiolytic Efficacy

Distinct Structural Features of Cyclothiazide Are Responsible for Effects on Peak Current Amplitude and Desensitization Kinetics at iGluR2

Stable expression of the human large‐conductance Ca2+‐activated K+ channel α‐ and β‐subunits in HEK293 cells

Identification of a novel voltage-gated Na+ channel rNa(v)1.5a in the rat hippocampal progenitor stem cell line HiB5

Pharmacological characterization of small-conductance Ca(2+)-activated K(+) channels stably expressed in HEK 293 cells

GABA sub(A) alpha 5 subunit-containing receptors do not contribute to reversal of inflammatory-induced spinal sensitization as indicated by the unique selectivity profile of the GABA sub(A) receptor allosteric modulator NS16085

Modulation of the Ca2+-dependent K+ channel, hslo, by the substituted diphenylurea NS 1608, paxilline and internal Ca2

Activation of human IK and SK Ca2+ -activated K+ channels by NS309 (6,7-dichloro-1H-indole-2,3-dione 3-oxime)

A Mosaic of Functional Kainate Receptors in Hippocampal Interneurons

Screening for lead compounds for Alzheimer's disease with dual mode of action, mimicking galanthamine at the human nicotinic receptors

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