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Sulfonamides as Selective NaV1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity | Journal of Medicinal Chemistry
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Sulfonamides as Selective NaV1.7 Inhibitors: Optimizing Potency, Pharmacokinetics, and Metabolic Properties to Obtain Atropisomeric Quinolinone (AM-0466) that Affords Robust in Vivo Activity | Journal of Medicinal Chemistry
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Chemical and Biological Tools for the Study of Voltage‐Gated Sodium Channels in Electrogenesis and Nociception - Elleman - 2022 - ChemBioChem - Wiley Online Library
Toxins | Free Full-Text | Tetrodotoxin: A New Strategy to Treat Visceral Pain?
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Challenges and Opportunities for Therapeutics Targeting the Voltage-Gated Sodium Channel Isoform NaV1.7 | Journal of Medicinal Chemistry
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