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Functional role of Kv1.1 and Kv1.3 channels in the neoplastic progression steps of three cancer cell lines, elucidated by scorpion peptides

International journal of biological macromolecules, 2018-05, Vol.111, p.1146-1155

2018

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Discovery, Characterization, and Effects on Renal Fluid and Electrolyte Excretion of the Kir4.1 Potassium Channel Pore Blocker, VU0134992

Molecular pharmacology, 2018-08, Vol.94 (2), p.926-937

2018

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Identification of WP1066, an inhibitor of JAK2 and STAT3, as a KV1.3 potassium channel blocker

British journal of pharmacology, 2021-07, Vol.178 (13), p.2617-2631

2021

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Pharmacology of a cloned potassium channel from mouse brain (MK-1) expressed in CHO cells : effects of blockers and an inactivation peptide

British journal of pharmacology, 1993-07, Vol.109 (3), p.725-735

1993

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Identification of WP1066, an inhibitor of JAK2 and STAT3, as a KV 1.3 potassium channel blocker

British journal of pharmacology, 2021-07, Vol.178 (13), p.2617-2631

2021

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Early increases in renal kallikrein secretion on administration of potassium or ATP‐sensitive potassium channel blockers in rats

British journal of pharmacology, 1999-11, Vol.128 (6), p.1275-1283

1999

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Variability of Potassium Channel Blockers in Mesobuthus eupeus Scorpion Venom with Focus on Kv1.1: AN INTEGRATED TRANSCRIPTOMIC AND PROTEOMIC STUDY

The Journal of biological chemistry, 2015-05, Vol.290 (19), p.12195-12209

2015

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Pharmacology of a cloned potassium channel from mouse brain (MK‐1) expressed in CHO cells: effects of blockers and an ‘nactivation peptide’

British journal of pharmacology, 1993-07, Vol.109 (3), p.725-735

1993

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Differential atrial versus ventricular activities of class III potassium channel blockers

The Journal of pharmacology and experimental therapeutics, 1998-04, Vol.285 (1), p.135

1998

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Effects of Aranidipine, a Novel Calcium Channel Blocker, on Mechanical Responses of the Isolated Rat Portal Vein: Comparison with Typical Calcium Channel Blockers and Potassium Channel Openers

Journal of cardiovascular pharmacology, 1997-02, Vol.29 (2), p.209-215

1997

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Variability of Potassium Channel Blockers in Mesobuthus eupeus Scorpion Venom with Focus on Kv1.1

The Journal of biological chemistry, 2015-05, Vol.290 (19), p.12195-12209

2015

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Anti-ischemic effects of the potassium channel activators pinacidil and cromakalim and the reversal of these effects with the potassium channel blocker glyburide

The Journal of pharmacology and experimental therapeutics, 1989-10, Vol.251 (1), p.98

1989

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Dispersion of ventricular repolarization and ventricular fibrillation in left ventricular hypertrophy: influence of selective potassium channel blockers

The Journal of pharmacology and experimental therapeutics, 2000-01, Vol.292 (1), p.381

2000

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An ATP-dependent potassium channel blocker antagonizes morphine analgesia

European journal of pharmacology, 1990-09, Vol.186 (2-3), p.377-378

1990

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Diuretic action of potassium channel blockers

European journal of clinical pharmacology, 1993-01, Vol.44 Suppl 1 (S1), p.S3-S5

Giebisch, G

1993

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Effects of inhibition of calcium and potassium currents in guinea‐pig cardiac contraction: comparison of β‐caryophyllene oxide, eugenol, and nifedipine

British journal of pharmacology, 2000-11, Vol.131 (6), p.1089-1096

2000

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Potassium channel blockers in multiple sclerosis: Neuronal K sub(v) channels and effects of symptomatic treatment

Pharmacology & therapeutics (Oxford), 2006-07, Vol.111 (1), p.224-259

2006

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ATP-Sensitive Potassium Channel Openers and Blockers in the Cardiovascular System: Physiology, Pharmacology, and Clinical Effects

Seminars in cardiothoracic and vascular anesthesia, 1998-09, Vol.2 (3), p.243-255

1998

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Effects of potassium channel blockers on CO2-induced slowly adapting pulmonary stretch receptor inhibition

The Journal of pharmacology and experimental therapeutics, 1999-09, Vol.290 (3), p.974

1999

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Pharmacological characterization of the discriminative stimulus effects of the potassium channel blocker 4-aminopyridine in rats

The Journal of pharmacology and experimental therapeutics, 2000-10, Vol.295 (1), p.382

2000

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Different mechanisms of relaxation of pig coronary artery to bradykinin and cromakalim are distinguished by potassium channel blockers

The Journal of pharmacology and experimental therapeutics, 1992-01, Vol.260 (1), p.248

1992

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Analysis of the vasorelaxant action of jatrophone in the isolated aorta of the rat: influence of potassium channel blockers

European journal of pharmacology, 1992-04, Vol.215 (1), p.75-81

1992

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Use of Cultured Human Neuroblastoma Cells in Rapid Discovery of the Voltage-gated Potassium-channel Blockers

Journal of pharmacy and pharmacology, 1994-09, Vol.46 (9), p.731-734

1994

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Sign Inversion in Photopharmacology: Incorporation of Cyclic Azobenzenes in Photoswitchable Potassium Channel Blockers and Openers

Angewandte Chemie (International ed.), 2019-10, Vol.58 (43), p.15421-15428

International ed. in English, 2019

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9‐Amino‐1,2,3,4‐tetrahydroacridine (THA) is a potent blocker of cardiac potassium channels

British journal of pharmacology, 1987-11, Vol.92 (3), p.521-525

Osterrieder, Wolfgang

1987

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Functional role of Kv1.1 and Kv1.3 channels in the neoplastic progression steps of three cancer cell lines, elucidated by scorpion peptides

Discovery, Characterization, and Effects on Renal Fluid and Electrolyte Excretion of the Kir4.1 Potassium Channel Pore Blocker, VU0134992

Identification of WP1066, an inhibitor of JAK2 and STAT3, as a KV1.3 potassium channel blocker

Pharmacology of a cloned potassium channel from mouse brain (MK-1) expressed in CHO cells : effects of blockers and an inactivation peptide

Identification of WP1066, an inhibitor of JAK2 and STAT3, as a KV 1.3 potassium channel blocker

Early increases in renal kallikrein secretion on administration of potassium or ATP‐sensitive potassium channel blockers in rats

Variability of Potassium Channel Blockers in Mesobuthus eupeus Scorpion Venom with Focus on Kv1.1: AN INTEGRATED TRANSCRIPTOMIC AND PROTEOMIC STUDY

Pharmacology of a cloned potassium channel from mouse brain (MK‐1) expressed in CHO cells: effects of blockers and an ‘nactivation peptide’

Differential atrial versus ventricular activities of class III potassium channel blockers

Effects of Aranidipine, a Novel Calcium Channel Blocker, on Mechanical Responses of the Isolated Rat Portal Vein: Comparison with Typical Calcium Channel Blockers and Potassium Channel Openers

Variability of Potassium Channel Blockers in Mesobuthus eupeus Scorpion Venom with Focus on Kv1.1

Anti-ischemic effects of the potassium channel activators pinacidil and cromakalim and the reversal of these effects with the potassium channel blocker glyburide

Dispersion of ventricular repolarization and ventricular fibrillation in left ventricular hypertrophy: influence of selective potassium channel blockers

An ATP-dependent potassium channel blocker antagonizes morphine analgesia

Diuretic action of potassium channel blockers

Effects of inhibition of calcium and potassium currents in guinea‐pig cardiac contraction: comparison of β‐caryophyllene oxide, eugenol, and nifedipine

Potassium channel blockers in multiple sclerosis: Neuronal K sub(v) channels and effects of symptomatic treatment

ATP-Sensitive Potassium Channel Openers and Blockers in the Cardiovascular System: Physiology, Pharmacology, and Clinical Effects

Effects of potassium channel blockers on CO2-induced slowly adapting pulmonary stretch receptor inhibition

Pharmacological characterization of the discriminative stimulus effects of the potassium channel blocker 4-aminopyridine in rats

Different mechanisms of relaxation of pig coronary artery to bradykinin and cromakalim are distinguished by potassium channel blockers

Analysis of the vasorelaxant action of jatrophone in the isolated aorta of the rat: influence of potassium channel blockers

Use of Cultured Human Neuroblastoma Cells in Rapid Discovery of the Voltage-gated Potassium-channel Blockers

Sign Inversion in Photopharmacology: Incorporation of Cyclic Azobenzenes in Photoswitchable Potassium Channel Blockers and Openers

9‐Amino‐1,2,3,4‐tetrahydroacridine (THA) is a potent blocker of cardiac potassium channels

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