Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lee, Hyosung | - |
dc.contributor.author | Park, Ki Duk | - |
dc.contributor.author | Yang, Xiao-Fang | - |
dc.contributor.author | Dustrude, Erik T. | - |
dc.contributor.author | Wilson, Sarah M. | - |
dc.contributor.author | Khanna, Rajesh | - |
dc.contributor.author | Kohn, Harold | - |
dc.date.accessioned | 2024-01-20T12:01:44Z | - |
dc.date.available | 2024-01-20T12:01:44Z | - |
dc.date.created | 2021-08-31 | - |
dc.date.issued | 2013-07-25 | - |
dc.identifier.issn | 0022-2623 | - |
dc.identifier.uri | https://pubs.kist.re.kr/handle/201004/127859 | - |
dc.description.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. | - |
dc.language | English | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | GATED SODIUM-CHANNELS | - |
dc.subject | SLOW INACTIVATION | - |
dc.subject | IDENTIFICATION | - |
dc.title | (Biphenyl-4-yl)methylammonium Chlorides: Potent Anticonvulsants That Modulate Na+ Currents | - |
dc.type | Article | - |
dc.identifier.doi | 10.1021/jm4007092 | - |
dc.description.journalClass | 1 | - |
dc.identifier.bibliographicCitation | JOURNAL OF MEDICINAL CHEMISTRY, v.56, no.14, pp.5931 - 5939 | - |
dc.citation.title | JOURNAL OF MEDICINAL CHEMISTRY | - |
dc.citation.volume | 56 | - |
dc.citation.number | 14 | - |
dc.citation.startPage | 5931 | - |
dc.citation.endPage | 5939 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.identifier.wosid | 000322503000023 | - |
dc.identifier.scopusid | 2-s2.0-84880890072 | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Medicinal | - |
dc.relation.journalResearchArea | Pharmacology & Pharmacy | - |
dc.type.docType | Article | - |
dc.subject.keywordPlus | GATED SODIUM-CHANNELS | - |
dc.subject.keywordPlus | SLOW INACTIVATION | - |
dc.subject.keywordPlus | IDENTIFICATION | - |
dc.subject.keywordAuthor | anticonvulsant | - |
dc.subject.keywordAuthor | epilepsy | - |
dc.subject.keywordAuthor | lacosamide | - |
dc.subject.keywordAuthor | sodium channel | - |
dc.subject.keywordAuthor | slow inactivation | - |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.