Methods and compounds for the treatment of mucus hypersecretion
    22.
    发明申请
    Methods and compounds for the treatment of mucus hypersecretion 失效
    用于治疗粘液分泌过多的方法和化合物

    公开(公告)号:US20070010447A1

    公开(公告)日:2007-01-11

    申请号:US11518213

    申请日:2006-09-11

    CPC classification number: A61K38/4886 A61K47/62 C07K14/33 C07K2319/33

    Abstract: A method of treating mucus hypersecretion, the causative factor in chronic obstructive pulmonary disease (COPD), asthma and other clinical conditions involving COPD, comprises administering a compound that inhibits exocytosis in mucus secreting cells or neurones that control or direct mucus secretion. Also described is a compound, for use in the treatment of hypersecretion of mucus, which inhibits mucus secretion by inhibiting mucus secretion by mucus secreting cells, and/or inhibiting neurotransmitter release from neuronal cells controlling or directing mucus secretion.

    Abstract translation: 一种治疗粘液分泌过多症的方法,慢性阻塞性肺疾病(COPD),哮喘和其它涉及COPD的临床病症的因素包括给予抑制或分泌粘液分泌细胞或神经元中的胞吐作用的化合物。 还描述了一种用于治疗粘液分泌过高的化合物,其通过抑制由分泌分泌细菌的粘液分泌而抑制粘液分泌,和/或抑制神经递质从控制或引导粘液分泌的神经元细胞释放。

    Fusion proteins
    23.
    发明授权
    Fusion proteins 有权
    融合蛋白

    公开(公告)号:US08399401B2

    公开(公告)日:2013-03-19

    申请号:US13239573

    申请日:2011-09-22

    Abstract: A single chain, polypeptide fusion protein, comprising: a non-cytotoxic protease, or a fragment thereof, which protease or protease fragment is capable of cleaving a protein of the exocytic fusion apparatus of a nociceptive sensory afferent; a Targeting Moiety that is capable of binding to a Binding Site on the nociceptive sensory afferent, which Binding Site is capable of undergoing endocytosis to be incorporated into an endosome within the nociceptive sensory afferent; a protease cleavage site at which site the fusion protein is cleavable by a protease, wherein the protease cleavage site is located between the non-cytotoxic protease or fragment thereof and the Targeting Moiety; a translocation domain that is capable of translocating the protease or protease fragment from within an endosome, across the endosomal membrane and into the cytosol of the nociceptive sensory afferent. Nucleic acids encoding the fusion proteins, methods of preparing same and uses thereof are also described.

    Abstract translation: 一种单链多肽融合蛋白,其包含:非细胞毒性蛋白酶或其片段,所述蛋白酶或蛋白酶片段能够切割伤害性感觉传入的胞外融合装置的蛋白质; 能够结合伤害性感觉传入的结合位点的靶向部位,该结合位点能够经历内吞作用以掺入伤害性感觉传入内的内体; 蛋白酶切割位点,其中融合蛋白可被蛋白酶切割,其中蛋白酶切割位点位于非细胞毒性蛋白酶或其片段与靶向部位之间; 能够将位于内体内的蛋白酶或蛋白酶片段穿过内体膜并转移到伤害性感觉传入物的胞质溶胶中的易位结构域。 还描述了编码融合蛋白的核酸,其制备方法及其用途。

    FUSION PROTEINS
    24.
    发明申请
    FUSION PROTEINS 有权
    融合蛋白

    公开(公告)号:US20120230975A1

    公开(公告)日:2012-09-13

    申请号:US13419381

    申请日:2012-03-13

    Abstract: A single chain, polypeptide fusion protein, comprising: a non-cytotoxic protease, or a fragment thereof, which protease or protease fragment can cleave a protein of the exocytic fusion apparatus of a nociceptive sensory afferent; a Targeting Moiety that can bind to a Binding Site on the nociceptive sensory afferent, which Binding Site can undergo endocytosis to be incorporated into an endosome within the nociceptive sensory afferent; a protease cleavage site at which site the fusion protein is cleavable by a protease, which is located between the non-cytotoxic protease and the Targeting Moiety; and a translocation domain that can translocate the protease or protease fragment from within an endosome, across the endosomal membrane and into the cytosol of the nociceptive sensory afferent; wherein the Targeting Moiety is BAM, β-endorphin, bradykinin, substance P, dynorphin and/or nociceptin. Nucleic acid sequences encoding the fusion proteins, methods of preparing same and uses thereof are also described.

    Abstract translation: 一种单链多肽融合蛋白,其包含:非细胞毒性蛋白酶或其片段,所述蛋白酶或蛋白酶片段可以切割伤害性感觉传入的胞外融合装置的蛋白质; 可以结合伤害性感觉传入物上的结合位点的靶向物质,该结合位点可以进行内吞作用以掺入伤害性感觉传入体内的内体; 蛋白酶切割位点,位于融合蛋白可被位于非细胞毒性蛋白酶和靶向部位之间的蛋白酶切割; 以及易位区域,其可以将位于内体内的蛋白酶或蛋白酶片段穿过内体膜并转移到伤害性感觉传入物的胞质溶胶中; 其中靶向部分是BAM,β-内啡肽,缓激肽,物质P,强啡肽和/或伤害感受肽。 还描述了编码融合蛋白的核酸序列,其制备方法及其用途。

    Fusion proteins
    25.
    发明授权
    Fusion proteins 有权
    融合蛋白

    公开(公告)号:US08067200B2

    公开(公告)日:2011-11-29

    申请号:US11792210

    申请日:2005-12-01

    Abstract: A single chain, polypeptide fusion protein, comprising: a non-cytotoxic protease, or a fragment thereof, which protease or protease fragment is capable of cleaving a protein of the exocytic fusion apparatus of a nociceptive sensory afferent; a Targeting Moiety that is capable of binding to a Binding Site on the nociceptive sensory afferent, which Binding Site is capable of undergoing endocytosis to be incorporated into an endosome within the nociceptive sensory afferent; a protease cleavage site at which site the fusion protein is cleavable by a protease, wherein the protease cleavage site is located between the non-cytotoxic protease or fragment thereof and the Targeting Moiety; and a translocation domain that is capable of translocating the protease or protease fragment from within an endosome, across the endosomal membrane and into the cytosol of the nociceptive sensory afferent. Nucleic acid sequences encoding the polypeptide fusion proteins, methods of preparing same and uses thereof are also described.

    Abstract translation: 一种单链多肽融合蛋白,其包含:非细胞毒性蛋白酶或其片段,所述蛋白酶或蛋白酶片段能够切割伤害性感觉传入的胞外融合装置的蛋白质; 能够结合伤害性感觉传入的结合位点的靶向部位,该结合位点能够经历内吞作用以掺入伤害性感觉传入内的内体; 蛋白酶切割位点,其中融合蛋白可被蛋白酶切割,其中蛋白酶切割位点位于非细胞毒性蛋白酶或其片段与靶向部位之间; 以及易位区域,其能够将位于内体内的蛋白酶或蛋白酶片段穿过内体膜并转移到伤害性感觉传入物的胞质溶胶中。 还描述了编码多肽融合蛋白的核酸序列,其制备方法及其用途。

    Clostridial toxin derivatives able to modify peripheral sensory afferent functions

    公开(公告)号:US20060051356A1

    公开(公告)日:2006-03-09

    申请号:US11234250

    申请日:2005-09-26

    Abstract: This invention describes a novel agent for the targeted control of a mammalian cell activity, in particular the agent is used to control the interaction of particular cell types with their external environment. The agent has applications as a pharmaceutical for the treatment of a variety of disorders. An agent according to the invention comprises three Domains B, T and E linked together in the following manner: Domain B-Domain T-Domain E where Domain B is the Binding Domain which binds the agent to a Binding Site on the cell which undergoes endocytosis to produce an endosome, Domain T is the Translocation Domain which translocates the agent (with or without the Binding Site) from within the endosome across the endosomal membrane into the cytosol of the cell, Domain E is the Effector Domain which inhibits the ability of the Recyclable Membrane Vesicles to transport the Integral Membrane Proteins to the surface of the cell.

    Door closer
    29.
    发明申请
    Door closer 有权
    闭门器

    公开(公告)号:US20050273975A1

    公开(公告)日:2005-12-15

    申请号:US11137681

    申请日:2005-05-25

    Applicant: Keith Foster

    Inventor: Keith Foster

    Abstract: A door closer includes an anchor assembly for mounting on a door frame, an actuator assembly for mounting within the thickness of a door which is hinged for movement between open and closed positions, an operating member coupled by a linkage to the anchor assembly and mounted for a range of movements between a retracted position and an extended position, a resilient driving apparatus arranged to exert a driving force on the operating member, a damper mechanism operatively connected to the operating member so as to damp movement of the operating member at least in a direction towards the retracted position, and a resilient thrust device arranged to exert an increased driving force on the operating member over a defined part of its range of movement as the operating member approaches the retracted position.

    Abstract translation: 门关闭器包括用于安装在门框上的锚固组件,用于安装在门的厚度内的致动器组件,门的厚度被铰接以在打开和关闭位置之间运动;操作构件通过联动装置联接到锚固组件, 在缩回位置和延伸位置之间的一系列运动;弹性驱动装置,其布置成在所述操作构件上施加驱动力;阻尼机构,其可操作地连接到所述操作构件,以便阻止所述操作构件的运动至少在 朝向缩回位置的方向,以及弹性推力装置,其布置成当操作构件接近缩回位置时,在其移动范围的限定部分上对操作构件施加增加的驱动力。

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