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A rat model of FOLFOX-induced neuropathy: effects of oral dimiracetam in comparison with duloxetine and pregabalin

Cancer chemotherapy and pharmacology, 2017-12, Vol.80 (6), p.1091-1103

2017

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Promotion of sleep by targeting the orexin system in rats, dogs and humans

Nature medicine, 2007-02, Vol.13 (2), p.150-155

2007

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Three different up-titration regimens of ponesimod, an S1P1 receptor modulator, in healthy subjects

Journal of clinical pharmacology, 2015-06, Vol.55 (6), p.688-697

2015

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Pharmacological Profile of MP-101, a Novel Non-racemic Mixture of R- and S-dimiracetam with Increased Potency in Rat Models of Cognition, Depression and Neuropathic Pain

Cells (Basel, Switzerland), 2022-12, Vol.11 (24), p.4027

2022

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A model of neuropathic pain induced by sorafenib in the rat: Effect of dimiracetam

Neurotoxicology (Park Forest South), 2015-09, Vol.50, p.101-107

2015

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Pharmacology of the urotensin-II receptor antagonist palosuran (ACT-058362; 1-[2-(4-benzyl-4-hydroxy-piperidin-1-yl)-ethyl]-3-(2-methyl-quinolin-4-yl)-urea sulfate salt): first demonstration of a pathophysiological role of the urotensin System

The Journal of pharmacology and experimental therapeutics, 2004-10, Vol.311 (1), p.204-212

2004

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UROTENSIN II MEDIATES ERK1 2 PHOSPHORYLATION AND PROLIFERATION IN GPR14-TRANSFECTED CELL LINES

Journal of receptors and signal transduction, 2002, Vol.22 (1-4), p.155-168

2002

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Day 2 Panel 1: Protecting the Child: Focus on Intimate Partner Violence and Custody Law

Columbia journal of gender and law, 2023-08, Vol.44 (1), p.176-209

2023

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Synthesis and Anti‐Hyperalgesic Efficacy of MP‐103, a Non‐Racemic Enantiomeric Mixture of a New 1,4‐Diazabicyclo[4.3.0]nonan‐9‐one

ChemistrySelect (Weinheim), 2024-08, Vol.9 (31), p.n/a

2024

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2-Imino-thiazolidin-4-one Derivatives as Potent, Orally Active S1P 1 Receptor Agonists

Journal of medicinal chemistry, 2010-05, Vol.53 (10), p.4198-4211

2010

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Effects of Dimiracetam on oxaliplatin-induced hyperalgesia and allodynia in the rat

Journal of clinical oncology, 2015-05, Vol.33 (15_suppl), p.e20650-e20650

2015

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Three different up-titration regimens of ponesimod, an S1P 1 receptor modulator, in healthy subjects: Journal of Clinical Pharmacology

Journal of clinical pharmacology, 2015-06, Vol.55 (6), p.688-697

2015

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New Cyclooxygenase-2/5-Lipoxygenase Inhibitors. 3. 7-tert-Butyl-2,3-dihydro-3,3-dimethylbenzofuran Derivatives as Gastrointestinal Safe Antiinflammatory and Analgesic Agents: Variations at the 5 Position

Journal of medicinal chemistry, 1998-08, Vol.41 (18), p.3515-3529

1998

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Novel S1P(1) receptor agonists--part 3: from thiophenes to pyridines

Journal of medicinal chemistry, 2014-01, Vol.57 (1), p.110-130

2014

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Novel S1P(1) receptor agonists--part 2: from bicyclo[3.1.0]hexane-fused thiophenes to isobutyl substituted thiophenes

Journal of medicinal chemistry, 2014-01, Vol.57 (1), p.78-97

2014

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Novel S1P1 Receptor Agonists - Part 2: From Bicyclo[3.1.0]hexane-Fused Thiophenes to Isobutyl Substituted Thiophenes

Journal of medicinal chemistry, 2014-01, Vol.57 (1), p.78-97

2014

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Novel S1P1 Receptor Agonists − Part 3: From Thiophenes to Pyridines

Journal of medicinal chemistry, 2014-01, Vol.57 (1), p.110-130

2014

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Novel S1P1 Receptor Agonists – Part 1: From Pyrazoles to Thiophenes

Journal of medicinal chemistry, 2013-12, Vol.56 (23), p.9737-9755

2013

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New Cyclooxygenase-2/5-Lipoxygenase Inhibitors. 2. 7-tert-Butyl-2,3-dihydro-3,3-dimethylbenzofuran Derivatives as Gastrointestinal Safe Antiinflammatory and Analgesic Agents: Variations of the Dihydrobenzofuran Ring

Journal of medicinal chemistry, 1998-03, Vol.41 (7), p.1124-1137

1998

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Novel S1P 1 Receptor Agonists - Part 2: From Bicyclo[3.1.0]hexane-Fused Thiophenes to Isobutyl Substituted Thiophenes

Journal of medicinal chemistry, 2014-01, Vol.57 (1), p.78-97

2014

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Novel S1P 1 Receptor Agonists – Part 1: From Pyrazoles to Thiophenes

Journal of medicinal chemistry, 2013-12, Vol.56 (23), p.9737-9755

2013

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Novel S1P 1 Receptor Agonists − Part 3: From Thiophenes to Pyridines

Journal of medicinal chemistry, 2014-01, Vol.57 (1), p.110-130

2014

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Synthesis and structure-activity relationships of N,N'-di-o-tolylguanidine analogs, high-affinity ligands for the haloperidol-sensitive .sigma. receptor

Journal of medicinal chemistry, 1990-09, Vol.33 (9), p.2421-2429

1990

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Reply to 'Promotion of sleep by targeting the orexin system in rats, dogs and humans'

Nature medicine, 2007-05, Vol.13 (5), p.526-526

2007

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A rat model of FOLFOX-induced neuropathy: effects of oral dimiracetam in comparison with duloxetine and pregabalin

Promotion of sleep by targeting the orexin system in rats, dogs and humans

Three different up-titration regimens of ponesimod, an S1P1 receptor modulator, in healthy subjects

Pharmacological Profile of MP-101, a Novel Non-racemic Mixture of R- and S-dimiracetam with Increased Potency in Rat Models of Cognition, Depression and Neuropathic Pain

A model of neuropathic pain induced by sorafenib in the rat: Effect of dimiracetam

Pharmacology of the urotensin-II receptor antagonist palosuran (ACT-058362; 1-[2-(4-benzyl-4-hydroxy-piperidin-1-yl)-ethyl]-3-(2-methyl-quinolin-4-yl)-urea sulfate salt): first demonstration of a pathophysiological role of the urotensin System

UROTENSIN II MEDIATES ERK1 2 PHOSPHORYLATION AND PROLIFERATION IN GPR14-TRANSFECTED CELL LINES

Day 2 Panel 1: Protecting the Child: Focus on Intimate Partner Violence and Custody Law

Synthesis and Anti‐Hyperalgesic Efficacy of MP‐103, a Non‐Racemic Enantiomeric Mixture of a New 1,4‐Diazabicyclo[4.3.0]nonan‐9‐one

2-Imino-thiazolidin-4-one Derivatives as Potent, Orally Active S1P 1 Receptor Agonists

Effects of Dimiracetam on oxaliplatin-induced hyperalgesia and allodynia in the rat

Three different up-titration regimens of ponesimod, an S1P 1 receptor modulator, in healthy subjects: Journal of Clinical Pharmacology

New Cyclooxygenase-2/5-Lipoxygenase Inhibitors. 3. 7-tert-Butyl-2,3-dihydro-3,3-dimethylbenzofuran Derivatives as Gastrointestinal Safe Antiinflammatory and Analgesic Agents: Variations at the 5 Position

Novel S1P(1) receptor agonists--part 3: from thiophenes to pyridines

New Cyclooxygenase-2/5-Lipoxygenase Inhibitors. 1. 7-tert-Butyl-2,3-dihydro-3,3-dimethylbenzofuran Derivatives as Gastrointestinal Safe Antiinflammatory and Analgesic Agents: Discovery and Variation of the 5-Keto Substituent

Novel S1P(1) receptor agonists--part 2: from bicyclo[3.1.0]hexane-fused thiophenes to isobutyl substituted thiophenes

Novel S1P1 Receptor Agonists - Part 2: From Bicyclo[3.1.0]hexane-Fused Thiophenes to Isobutyl Substituted Thiophenes

Novel S1P1 Receptor Agonists − Part 3: From Thiophenes to Pyridines

Novel S1P1 Receptor Agonists – Part 1: From Pyrazoles to Thiophenes

New Cyclooxygenase-2/5-Lipoxygenase Inhibitors. 2. 7-tert-Butyl-2,3-dihydro-3,3-dimethylbenzofuran Derivatives as Gastrointestinal Safe Antiinflammatory and Analgesic Agents: Variations of the Dihydrobenzofuran Ring

Novel S1P 1 Receptor Agonists - Part 2: From Bicyclo[3.1.0]hexane-Fused Thiophenes to Isobutyl Substituted Thiophenes

Novel S1P 1 Receptor Agonists – Part 1: From Pyrazoles to Thiophenes

Novel S1P 1 Receptor Agonists − Part 3: From Thiophenes to Pyridines

Synthesis and structure-activity relationships of N,N'-di-o-tolylguanidine analogs, high-affinity ligands for the haloperidol-sensitive .sigma. receptor

Reply to 'Promotion of sleep by targeting the orexin system in rats, dogs and humans'

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