Cargando…
Physical basis of specificity and delayed binding of a subtype selective sodium channel inhibitor
Nerve and muscle signalling is controlled by voltage-gated sodium (Nav) channels which are the targets of local anesthetics, anti-epileptics and anti-arrythmics. Current medications do not selectively target specific types of Nav found in the body, but compounds that do so have the potential to be b...
Autor principal: | Corry, Ben |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778059/ https://www.ncbi.nlm.nih.gov/pubmed/29358762 http://dx.doi.org/10.1038/s41598-018-19850-9 |
Ejemplares similares
-
Na(+)/Ca(2+) selectivity in the bacterial voltage-gated sodium channel NavAb
por: Corry, Ben
Publicado: (2013) -
Locating the Route of Entry and Binding Sites of Benzocaine and Phenytoin in a Bacterial Voltage Gated Sodium Channel
por: Martin, Lewis J., et al.
Publicado: (2014) -
Discovery and molecular basis of subtype-selective cyclophilin inhibitors
por: Peterson, Alexander A., et al.
Publicado: (2022) -
Investigating the size and dynamics of voltage-gated sodium channel fenestrations: A molecular dynamics study
por: Kaczmarski, Joe A, et al.
Publicado: (2014) -
Basis of substrate binding and conservation of selectivity in the CLC family of channels and transporters
por: Picollo, Alessandra, et al.
Publicado: (2009)