A series of imidazol-1-ylethylindazole sodium channel ligands were developed and optimized for sodium channel inhibition and in vitro neuroprotective activity. The molecules exhibited displacement of a radiolabeled sodium channel ligand and selectivity for blockade of the inactivated state of cloned neuronal Nav channels. Metabolically stable analogue 6 was able to protect retinal ganglion cells during optic neuritis in a mouse model of multiple sclerosis.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010550 | PMC |
http://dx.doi.org/10.1021/jm401881q | DOI Listing |
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