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    Discovery and Optimization of Selective Na<sub>v</sub>1.8 Modulator Series That Demonstrate Efficacy in Preclinical Models of Pain

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    Voltage-gated sodium channels, in particular Na<sub>v</sub>1.8, can be targeted for the treatment of neuropathic and inflammatory pain. Herein, we described the optimization of Na<sub>v</sub>1.8 modulator series to deliver subtype selective, state, and use-dependent chemical matter that is efficacious in preclinical models of neuropathic and inflammatory pain
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