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Citral inhibits the nociception in the rat formalin test: effect of metformin and blockers of opioid receptor and the NO-cGMP-K + channel pathway

Canadian journal of physiology and pharmacology, 2022-04, Vol.100 (4), p.306

2022

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Tuning Photochromic Ion Channel Blockers

ACS chemical neuroscience, 2011-09, Vol.2 (9), p.536-543

2011

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XE991 and Linopirdine Are State-Dependent Inhibitors for Kv7/KCNQ Channels that Favor Activated Single Subunits

The Journal of pharmacology and experimental therapeutics, 2017-07, Vol.362 (1), p.177

2017

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Engineering a Stable and Selective Peptide Blocker of the Kv1.3 Channel in T Lymphocytes

Molecular pharmacology, 2009-04, Vol.75 (4), p.762-773

2009

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Relaxation effect of narirutin on rat mesenteric arteries via nitric oxide release and activation of voltage-gated potassium channels

European journal of pharmacology, 2021-08, Vol.905, p.174190-174190, Article 174190

2021

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Role of Kv7.2/Kv7.3 and M 1 muscarinic receptors in the regulation of neuronal excitability in hiPSC-derived neurons

European journal of pharmacology, 2019-09, Vol.858, p.172474

2019

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Vm24, a natural immunosuppressive peptide, potently and selectively blocks Kv1.3 potassium channels of human T cells

Molecular pharmacology, 2012-09, Vol.82 (3), p.372-382

2012

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NS6180, a new K(Ca) 3.1 channel inhibitor prevents T-cell activation and inflammation in a rat model of inflammatory bowel disease

British journal of pharmacology, 2013-01, Vol.168 (2), p.432

2013

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Involvement of Potassium Channels and Calcium-Independent Mechanisms in Hydrogen Sulfide-Induced Relaxation of Rat Mesenteric Small Arteries

The Journal of pharmacology and experimental therapeutics, 2016-01, Vol.356 (1), p.53

2016

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High-Throughput Screening Reveals a Small-Molecule Inhibitor of the Renal Outer Medullary Potassium Channel and Kir7.1

Molecular pharmacology, 2009-11, Vol.76 (5), p.1094-1103

2009

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The cardioprotective effect of naringenin against ischemia-reperfusion injury through activation of ATP-sensitive potassium channel in rat

Canadian journal of physiology and pharmacology, 2016-09, Vol.94 (9), p.973

2016

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Role of the NO-cGMP-K + channels pathway in the peripheral antinociception induced by α-bisabolol

Canadian journal of physiology and pharmacology, 2021-10, Vol.99 (10), p.1048

2021

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Molecular basis involved in the blocking effect of antidepressant metergoline on C-type inactivation of Kv1.4 channel

Neuropharmacology, 2019-03, Vol.146, p.65-73

2019

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Kir Channel Blockages by Proflavine Derivatives via Multiple Modes of Interaction

Molecular pharmacology, 2018-06, Vol.93 (6), p.592-600

2018

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Inhibition of voltage-gated potassium channels mediates uncarboxylated osteocalcin-regulated insulin secretion in rat pancreatic β cells

European journal of pharmacology, 2016-04, Vol.777, p.41-48

2016

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Vascular KCNQ potassium channels as novel targets for the control of mesenteric artery constriction by vasopressin, based on studies in single cells, pressurized arteries, and in vivo measurements of mesenteric vascular resistance

The Journal of pharmacology and experimental therapeutics, 2008-05, Vol.325 (2), p.475

2008

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The Kv1.3 channel blocker Vm24 enhances muscle glucose transporter 4 mobilization but does not reduce body-weight gain in diet-induced obese male rats

Life sciences (1973), 2017-07, Vol.181, p.23-30

2017

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Roles of K+ and cation channels in ORL-1 receptor-mediated depression of neuronal excitability and epileptic activities in the medial entorhinal cortex

Neuropharmacology, 2019-06, Vol.151, p.144-158

2019

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Synthesis and pharmacological evaluation of piperidine (piperazine)-substituted benzoxazole derivatives as multi-target antipsychotics

Bioorganic & medicinal chemistry letters, 2015-11, Vol.25 (22), p.5299-5305

2015

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Design of PAP-1, a Selective Small Molecule Kv1.3 Blocker, for the Suppression of Effector Memory T Cells in Autoimmune Diseases

Molecular pharmacology, 2005-11, Vol.68 (5), p.1254-1270

2005

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Hesperidin inhibits glutamate release and exerts neuroprotection against excitotoxicity induced by kainic acid in the hippocampus of rats

Neurotoxicology (Park Forest South), 2015-09, Vol.50, p.157-169

2015

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In vitro evidence that endothelium-dependent vasodilatation induced by clozapine is mediated by an ATP-sensitive potassium channel

Pharmacological reports, 2019-06, Vol.71 (3), p.522-527

2019

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Novel Inhibitors of Staphyloxanthin Virulence Factor in Comparison with Linezolid and Vancomycin versus Methicillin-Resistant, Linezolid-Resistant, and Vancomycin-Intermediate Staphylococcus aureus Infections in Vivo

Journal of medicinal chemistry, 2017-10, Vol.60 (19), p.8145-8159

2017

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Antiarrhythmic Mechanisms of SK Channel Inhibition in the Rat Atrium

Journal of cardiovascular pharmacology, 2015-08, Vol.66 (2), p.165-176

2015

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Dihydropyrazolopyrimidines containing benzimidazoles as K(V)1.5 potassium channel antagonists

Bioorganic & medicinal chemistry letters, 2009-09, Vol.19 (18), p.5469-5473

2009

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1 – 25 von 2.093

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Citral inhibits the nociception in the rat formalin test: effect of metformin and blockers of opioid receptor and the NO-cGMP-K + channel pathway

Tuning Photochromic Ion Channel Blockers

XE991 and Linopirdine Are State-Dependent Inhibitors for Kv7/KCNQ Channels that Favor Activated Single Subunits

Engineering a Stable and Selective Peptide Blocker of the Kv1.3 Channel in T Lymphocytes

Relaxation effect of narirutin on rat mesenteric arteries via nitric oxide release and activation of voltage-gated potassium channels

Role of Kv7.2/Kv7.3 and M 1 muscarinic receptors in the regulation of neuronal excitability in hiPSC-derived neurons

Vm24, a natural immunosuppressive peptide, potently and selectively blocks Kv1.3 potassium channels of human T cells

NS6180, a new K(Ca) 3.1 channel inhibitor prevents T-cell activation and inflammation in a rat model of inflammatory bowel disease

Involvement of Potassium Channels and Calcium-Independent Mechanisms in Hydrogen Sulfide-Induced Relaxation of Rat Mesenteric Small Arteries

High-Throughput Screening Reveals a Small-Molecule Inhibitor of the Renal Outer Medullary Potassium Channel and Kir7.1

The cardioprotective effect of naringenin against ischemia-reperfusion injury through activation of ATP-sensitive potassium channel in rat

Role of the NO-cGMP-K + channels pathway in the peripheral antinociception induced by α-bisabolol

Molecular basis involved in the blocking effect of antidepressant metergoline on C-type inactivation of Kv1.4 channel

Kir Channel Blockages by Proflavine Derivatives via Multiple Modes of Interaction

Inhibition of voltage-gated potassium channels mediates uncarboxylated osteocalcin-regulated insulin secretion in rat pancreatic β cells

Vascular KCNQ potassium channels as novel targets for the control of mesenteric artery constriction by vasopressin, based on studies in single cells, pressurized arteries, and in vivo measurements of mesenteric vascular resistance

The Kv1.3 channel blocker Vm24 enhances muscle glucose transporter 4 mobilization but does not reduce body-weight gain in diet-induced obese male rats

Roles of K+ and cation channels in ORL-1 receptor-mediated depression of neuronal excitability and epileptic activities in the medial entorhinal cortex

Synthesis and pharmacological evaluation of piperidine (piperazine)-substituted benzoxazole derivatives as multi-target antipsychotics

Design of PAP-1, a Selective Small Molecule Kv1.3 Blocker, for the Suppression of Effector Memory T Cells in Autoimmune Diseases

Hesperidin inhibits glutamate release and exerts neuroprotection against excitotoxicity induced by kainic acid in the hippocampus of rats

In vitro evidence that endothelium-dependent vasodilatation induced by clozapine is mediated by an ATP-sensitive potassium channel

Novel Inhibitors of Staphyloxanthin Virulence Factor in Comparison with Linezolid and Vancomycin versus Methicillin-Resistant, Linezolid-Resistant, and Vancomycin-Intermediate Staphylococcus aureus Infections in Vivo

Antiarrhythmic Mechanisms of SK Channel Inhibition in the Rat Atrium

Dihydropyrazolopyrimidines containing benzimidazoles as K(V)1.5 potassium channel antagonists

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