Relationship Between Structure and Sodium Channel Blockade by Lidocaine and Its Amino-Alkyl Derivatives
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Cardiology and Cardiovascular Medicine,Pharmacology
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Comparison of Gating Properties and Use-Dependent Block of Nav1.5 and Nav1.7 Channels by Anti-Arrhythmics Mexiletine and Lidocaine;PLOS ONE;2015-06-11
2. Investigation of the effects of the novel anticonvulsant compound carisbamate (RWJ-333369) on rat piriform cortical neurones in vitro;British Journal of Pharmacology;2009-02-18
3. Inhibition of skeletal muscle sodium currents by mexiletine analogues: specific hydrophobic interactions rather than lipophilia per se account for drug therapeutic profile;Naunyn-Schmiedeberg's Archives of Pharmacology;2003-03
4. Block of Wild-Type and Inactivation-Deficient Cardiac Sodium Channels IFM/QQQ Stably Expressed in Mammalian Cells;Biophysical Journal;2000-12
5. Sodium Channel Blockers and Activators;Pharmacology of Ionic Channel Function: Activators and Inhibitors;2000
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