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dc.contributor.authorLee, Hyosung-
dc.contributor.authorPark, Ki Duk-
dc.contributor.authorYang, Xiao-Fang-
dc.contributor.authorDustrude, Erik T.-
dc.contributor.authorWilson, Sarah M.-
dc.contributor.authorKhanna, Rajesh-
dc.contributor.authorKohn, Harold-
dc.date.accessioned2024-01-20T12:01:44Z-
dc.date.available2024-01-20T12:01:44Z-
dc.date.created2021-08-31-
dc.date.issued2013-07-25-
dc.identifier.issn0022-2623-
dc.identifier.urihttps://pubs.kist.re.kr/handle/201004/127859-
dc.description.abstractWe 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.-
dc.languageEnglish-
dc.publisherAMER CHEMICAL SOC-
dc.subjectGATED SODIUM-CHANNELS-
dc.subjectSLOW INACTIVATION-
dc.subjectIDENTIFICATION-
dc.title(Biphenyl-4-yl)methylammonium Chlorides: Potent Anticonvulsants That Modulate Na+ Currents-
dc.typeArticle-
dc.identifier.doi10.1021/jm4007092-
dc.description.journalClass1-
dc.identifier.bibliographicCitationJOURNAL OF MEDICINAL CHEMISTRY, v.56, no.14, pp.5931 - 5939-
dc.citation.titleJOURNAL OF MEDICINAL CHEMISTRY-
dc.citation.volume56-
dc.citation.number14-
dc.citation.startPage5931-
dc.citation.endPage5939-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.identifier.wosid000322503000023-
dc.identifier.scopusid2-s2.0-84880890072-
dc.relation.journalWebOfScienceCategoryChemistry, Medicinal-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.type.docTypeArticle-
dc.subject.keywordPlusGATED SODIUM-CHANNELS-
dc.subject.keywordPlusSLOW INACTIVATION-
dc.subject.keywordPlusIDENTIFICATION-
dc.subject.keywordAuthoranticonvulsant-
dc.subject.keywordAuthorepilepsy-
dc.subject.keywordAuthorlacosamide-
dc.subject.keywordAuthorsodium channel-
dc.subject.keywordAuthorslow inactivation-
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