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Heterocyclic derivatives used as Nav1.7 and Nav1.8 blockers

机译:用作NAV1.7和NAV1.8阻拦者的杂环衍生物

摘要

The present invention relates to a heterocyclic derivative having blocking activity of translocation-opening sodium channels such as Nav1.7 and Nav1.8 channels, and useful for the treatment or prevention of translocation-opening sodium channel-related diseases and disorders. The present invention also relates to a pharmaceutical composition comprising the compound, and the use of the compound and composition for the prevention or treatment of a dislocation-apparent sodium channel-related disease.
机译:本发明涉及杂环衍生物,其具有阻断易于分配的钠通道的活性,例如NAV1.7和NAV1.8通道,可用于治疗或预防易位开口钠通道相关疾病和病症。 本发明还涉及包含该化合物的药物组合物,以及用于预防或治疗脱位表观钠通道相关疾病的化合物和组合物的使用。

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