Potent and selective inhibitors of NaV1.3 and NaV1.7
    2.
    发明授权
    Potent and selective inhibitors of NaV1.3 and NaV1.7 有权
    NaV1.3和NaV1.7的有效和选择性抑制剂

    公开(公告)号:US09340590B2

    公开(公告)日:2016-05-17

    申请号:US14005135

    申请日:2012-03-16

    摘要: Disclosed is a composition of matter comprising an isolated polypeptide, which is a peripherally-restricted Nav1.7 inhibitor. In some disclosed embodiments, the isolated polypeptide is an inhibitor of Nav1.7 and/or Nav1.3. Other embodiments are conjugated embodiments of the inventive composition of matter and pharmaceutical compositions containing the inventive composition of matter. Isolated nucleic acids encoding some embodiments of inventive polypeptides and expression vectors, and recombinant host cells containing them are disclosed. A method of treating or preventing pain is also disclosed.

    摘要翻译: 公开了包含分离的多肽的物质组合物,其是外周限制的Nav1.7抑制剂。 在一些公开的实施方案中,分离的多肽是Nav1.7和/或Nav1.3的抑制剂。 其它实施方案是本发明组合物和包含本发明组合物的药物组合物的共轭实施方案。 公开了编码本发明多肽和表达载体的一些实施方案的分离的核酸,以及含有它们的重组宿主细胞。 还公开了治疗或预防疼痛的方法。

    POTENT AND SELECTIVE INHIBITORS OF NAV1.3 AND NAV1.7
    3.
    发明申请
    POTENT AND SELECTIVE INHIBITORS OF NAV1.3 AND NAV1.7 有权
    NAV1.3和NAV1.7的POTENT和选择性抑制剂

    公开(公告)号:US20140073577A1

    公开(公告)日:2014-03-13

    申请号:US14005135

    申请日:2012-03-16

    IPC分类号: C07K14/435 A61K47/48

    摘要: Disclosed is a composition of matter comprising an isolated polypeptide, which is a peripherally-restricted Nav1.7 inhibitor. In some disclosed embodiments, the isolated polypeptide is an inhibitor of Nav1.7 and/or Nav1.3. Other embodiments are conjugated embodiments of the inventive composition of matter and pharmaceutical compositions containing the inventive composition of matter. Isolated nucleic acids encoding some embodiments of inventive polypeptides and expression vectors, and recombinant host cells containing them are disclosed. A method of treating or preventing pain is also disclosed.

    摘要翻译: 公开了包含分离的多肽的物质组合物,其是外周限制的Nav1.7抑制剂。 在一些公开的实施方案中,分离的多肽是Nav1.7和/或Nav1.3的抑制剂。 其它实施方案是本发明组合物和包含本发明组合物的药物组合物的共轭实施方案。 公开了编码本发明多肽和表达载体的一些实施方案的分离的核酸,以及含有它们的重组宿主细胞。 还公开了治疗或预防疼痛的方法。