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- W2050649679 abstract "The synthesis and pharmacological characterization of a novel furan-based class of voltage-gated sodium channel blockers is reported. Compounds were evaluated for their ability to block the tetrodotoxin-resistant sodium channel Nav1.8 (PN3) as well as the Nav1.2 and Nav1.5 subtypes. Benchmark compounds from this series possessed enhanced potency, oral bioavailability, and robust efficacy in a rodent model of neuropathic pain, together with improved CNS and cardiovascular safety profiles compared to the clinically used sodium channel blockers mexiletine and lamotrigine." @default.
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- W2050649679 date "2008-06-01" @default.
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- W2050649679 title "Discovery of potent furan piperazine sodium channel blockers for treatment of neuropathic pain" @default.
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- W2050649679 doi "https://doi.org/10.1016/j.bmc.2008.05.003" @default.
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