(Biphenyl-4-yl)methylammonium Chlorides: Potent Anticonvulsants That Modulate Na+ Currents

Authors
Lee, HyosungPark, Ki DukYang, Xiao-FangDustrude, Erik T.Wilson, Sarah M.Khanna, RajeshKohn, Harold
Issue Date
2013-07-25
Publisher
AMER CHEMICAL SOC
Citation
JOURNAL OF MEDICINAL CHEMISTRY, v.56, no.14, pp.5931 - 5939
Abstract
We have reported that compounds containing a biaryl linked unit (Ar-X-Ar') modulated Na+ currents by promoting slow inactivation and fast inactivation processes and by inducing frequency (use)-dependent inhibition of Na+ currents. These electrophysiological properties have been drugs. In this study, we demonstrate that the readily accessible associated with the mode of action of several antiepileptic (biphenyl-4-yl)methylammonium chlorides (compound class B) exhibited a broad range of anticonvulsant activities in animal models, and in the maximal electroshock seizure test the activity of (3'-trifluoromethoxybiphenyl-4-yl)methylammonium chloride (8) exceeded that of phenobarbital and phenytoin upon oral administration to rats. Electrophysiological studies of 8 using mouse catecholamine A-differentiated cells and rat embryonic cortical neurons confirmed that 8 promoted slow and fast inactivation in both cell types but did not affect the frequency (use)-dependent block of Na+ currents.
Keywords
GATED SODIUM-CHANNELS; SLOW INACTIVATION; IDENTIFICATION; GATED SODIUM-CHANNELS; SLOW INACTIVATION; IDENTIFICATION; anticonvulsant; epilepsy; lacosamide; sodium channel; slow inactivation
ISSN
0022-2623
URI
https://pubs.kist.re.kr/handle/201004/127859
DOI
10.1021/jm4007092
Appears in Collections:
KIST Article > 2013
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