| Literature DB >> 26114759 |
François Crestey1, Kristen Frederiksen1, Henrik S Jensen1, Kim Dekermendjian1, Peter H Larsen1, Jesper F Bastlund1, Dunguo Lu2, Henry Liu2, Charles R Yang2, Morten Grunnet1, Niels Svenstrup1.
Abstract
Voltage-gated sodium channels (Nav) are crucial to the initiation and propagation of action potentials (APs) in electrically excitable cells, and during the past decades they have received considerable attention due to their therapeutic potential. Here, we report for the first time the synthesis and the electrophysiological evaluation of 16 ligands based on a 2-methylbenzamide scaffold that have been identified as Nav1.1 modulators. Among these compounds, N,N'-(1,3-phenylene)bis(2-methylbenzamide) (3a) has been selected and evaluated in ex-vivo experiments in order to estimate the activation impact of such a compound profile. It appears that 3a increases the Nav1.1 channel activity although its overall impact remains moderate. Altogether, our preliminary results provide new insights into the development of small molecule activators targeting specifically Nav1.1 channels to design potential drugs for treating CNS diseases.Entities:
Keywords: 2-Methylbenzamide derivatives; Nav1.1 modulator; brain slices; fast-spiking interneurons; voltage-gated sodium channels
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Year: 2015 PMID: 26114759 DOI: 10.1021/acschemneuro.5b00147
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418