Targeting the Kv11.1 (hERG) channel with allosteric modulators. Synthesis and biological evaluation of three novel series of LUF7346 derivatives
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Title
Targeting the Kv11.1 (hERG) channel with allosteric modulators. Synthesis and biological evaluation of three novel series of LUF7346 derivatives
Authors
Keywords
K, v, 11.1 (hERG) channel, Allosteric modulation, LUF7346, Cardiotoxicity, Dofetilide, Human induced pluripotent stem cells (hiPSCs), hiPSC-derived cardiomyocytes
Journal
EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
Volume 212, Issue -, Pages 113033
Publisher
Elsevier BV
Online
2020-11-21
DOI
10.1016/j.ejmech.2020.113033
References
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Related references
Note: Only part of the references are listed.- An Update on the Structure of hERG
- (2020) Andrew Butler et al. Frontiers in Pharmacology
- LUF7244 plus Dofetilide Rescues Aberrant Kv11.1 Trafficking and Produces Functional IKv11.1
- (2020) Muge Qile et al. MOLECULAR PHARMACOLOGY
- LUF7244, an allosteric modulator/activator of K v 11.1 channels, counteracts dofetilide‐induced TdP arrhythmia in the chronic atrioventricular block dog model
- (2019) Muge Qile et al. BRITISH JOURNAL OF PHARMACOLOGY
- Trigger vs. Substrate: Multi-Dimensional Modulation of QT-Prolongation Associated Arrhythmic Dynamics by a hERG Channel Activator
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- Dissociative States: hERG Channel (Kv11.1) Modulators That Enhance Dissociation of Drugs From Their Blocking Receptor
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- Allosteric Modulation of Kv11.1 (hERG) Channels Protects Against Drug-Induced Ventricular Arrhythmias
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- Identification and Characterization of a Compound That Protects Cardiac Tissue from Human Ether-à-go-go-related Gene (hERG)-related Drug-induced Arrhythmias
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- Enhanced Repolarization Capacity: New Potential Antiarrhythmic Strategy Based on hERG Channel Activation
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