Distinct local anesthetic affinities in Na+ channel subtypes
Author:
Publisher
Elsevier BV
Subject
Biophysics
Cited by 55 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. The citrus flavanone hesperetin preferentially inhibits slow‐inactivating currents of a long QT syndrome type 3 syndrome Na + channel mutation;British Journal of Pharmacology;2019-03-27
2. Fast-onset lidocaine block of rat Na V1.4 channels suggests involvement of a second high-affinity open state;Biochimica et Biophysica Acta (BBA) - Biomembranes;2016-06
3. 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
4. N-Aryl-2,6-dimethylbenzamides, a New Generation of Tocainide Analogues as Blockers of Skeletal Muscle Voltage-Gated Sodium Channels;Journal of Medicinal Chemistry;2014-03-07
5. Searching for novel anti-myotonic agents: Pharmacophore requirement for use-dependent block of skeletal muscle sodium channels by N-benzylated cyclic derivatives of tocainide;Neuromuscular Disorders;2012-01
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