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Hydrophobic Drug/Toxin Binding Sites in Voltage-Dependent K(+) and Na(+) Channels

In the Na(v) channel family the lipophilic drugs/toxins binding sites and the presence of fenestrations in the channel pore wall are well defined and categorized. No such classification exists in the much larger K(v) channel family, although certain lipophilic compounds seem to deviate from binding...

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Detalles Bibliográficos
Autores principales: Van Theemsche, Kenny M., Van de Sande, Dieter V., Snyders, Dirk J., Labro, Alain J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243439/
https://www.ncbi.nlm.nih.gov/pubmed/32499709
http://dx.doi.org/10.3389/fphar.2020.00735

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