Dofetilide
Chemical Name: 1-(4-Methanesulphonamidophenoxy)-2-[N-(4-methanesulphonamidophenethyl)-N-methylamino]ethane
Purity: ≥99%
Biological Activity
Dofetilide is a selective potassium channel blocker. Blocks KV11.1 (hERG) channels; inhibits the rapid delayed-rectifier K+ current (IKr). Displays class III antiarrhythmic properties.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Additional Information
Background References
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UK-68,798: a novel, potent and highly selective class III antiarrhythmic agent which blocks potassium channels in cardiac cells.
Gwilt et al.
J.Pharmacol.Exp.Ther., 1991;256:318 -
[3H]Dofetilide binding in SHSY5Y and HEK293 cells expressing a HERG-like K+ channel.
Finlayson et al.
Eur.J.Pharmacol., 2001;412:203 -
Voltage- and time-dependent block of delayed K+ current in cardiac myocytes by dofet.
Carmeliet
J.Pharmacol.Exp.Ther., 1992;262:809 -
Antiarrhythmic Effects of Combining Dofetilide and Ranolazine in a Model of Acutely Induced Atrial Fibrillation in Horses.
Helena Carstensen, Line Kjær, Maria Mathilde Haugaard, Mette Flethøj, Eva Zander Hesselkil, Jørgen K Kanters, Steen Pehrson, Rikke Buhl, Thomas Jespersen
Journal of Cardiovascular Pharmacology, 2018;0(0):1533-4023.
Product Datasheets
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Citations for Dofetilide
The citations listed below are publications that use Tocris products. Selected citations for Dofetilide include:
5 Citations: Showing 1 - 5
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Reengineering an Antiarrhythmic Drug Using Patient hiPSC Cardiomyocytes to Improve Therapeutic Potential and Reduce Toxicity.
Authors: Mark Et al.
Cell Stem Cell 2020;27:813-821.e6
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Effects of UK 68798 and RS 43285 on atrial fibrillatory rate in a horse model of acutely induced atrial fibrillation.
Authors: Carstensen Et al.
J Cardiovasc Electrophysiol 2019;30:596
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An Automated Platform for Assessment of Congenital and Drug-Induced Arrhythmia with hiPSC-Derived Cardiomyocytes.
Authors: McKeithan Et al.
Front Physiol 2017;8:766
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Drug delivery to the human and mouse uterus using immunoliposomes targeted to the oxytocin receptor.
Authors: Roger Et al.
Am J Obstet Gynecol 2017;216:283.e1-283.e14
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Development of a selective small-molecule inhibitor of Kir1.1, the renal outer medullary potassium channel.
Authors: Bhave Et al.
Mol Pharmacol 2011;79:42
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