Published in J Neurophysiol on June 05, 2013
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A pharmacophore derived phenytoin analogue with increased affinity for slow inactivated sodium channels exhibits a desired anticonvulsant profile. Neuropharmacology (2006) 0.92
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Discovery of diphenyl amine based sodium channel blockers, effective against hNav1.2. Bioorg Med Chem (2006) 0.84
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Comparative molecular field analysis and synthetic validation of a hydroxyamide-propofol binding and functional block of neuronal voltage-dependent sodium channels. Bioorg Med Chem (2008) 0.79
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A highly efficient microfluidic nano biochip based on nanostructured nickel oxide. Nanoscale (2013) 0.79
In situ-produced 7-chlorokynurenate has different effects on evoked responses in rats with limbic epilepsy in comparison to naive controls. Epilepsia (2005) 0.78
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Synthesis and biological evaluation of a fluorescent analog of phenytoin as a potential inhibitor of neuropathic pain and imaging agent. Bioorg Med Chem (2012) 0.78
Reversal of neuropathic pain by alpha-hydroxyphenylamide: a novel sodium channel antagonist. Neuropharmacology (2006) 0.78
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