1151513-01-7Relevant articles and documents
Imidazol-1-ylethylindazole voltage-gated sodium channel ligands are neuroprotective during optic neuritis in a mouse model of multiple sclerosis
Browne, Lorcan,Lidster, Katie,Al-Izki, Sarah,Clutterbuck, Lisa,Posada, Cristina,Chan, A. W. Edith,Riddall, Dieter,Garthwaite, John,Baker, David,Selwood, David L.
, p. 2942 - 2952 (2014)
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.
Oxadiazolylindazole sodium channel modulators are neuroprotective toward hippocampal neurones
Clutterbuck, Lisa A.,Posada, Cristina Garcia,Visintin, Cristina,Riddall, Dieter R.,Lancaster, Barrie,Gane, Paul J.,Garthwaite, John,Selwood, David L.
experimental part, p. 2694 - 2707 (2010/03/03)
We report the discovery of a new class of neuroprotective voltage-dependent sodium channel modulators exemplified by (5-(1-benzyl-1H-indazol-3-yl)-1,2,4- oxadiazol-3-yl)methanamine 11 (CFM1178). The compounds were inhibitors of [ 14C]guanidiniu