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The external pore loop interacts with S6 and S3-S4 linker in domain 4 to assume an essential role in gating control and anticonvulsant action in the Na(+) channel

Carbamazepine, phenytoin, and lamotrigine are widely prescribed anticonvulsants in neurological clinics. These drugs bind to the same receptor site, probably with the diphenyl motif in their structure, to inhibit the Na(+) channel. However, the location of the drug receptor remains controversial. In...

詳細記述

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書誌詳細
主要な著者: Yang, Ya-Chin, Hsieh, Jui-Yi, Kuo, Chung-Chin
フォーマット: Artigo
言語:Inglês
出版事項: The Rockefeller University Press 2009
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC2717694/
https://ncbi.nlm.nih.gov/pubmed/19635852
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1085/jgp.200810158
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