Modified proteases that inhibit complement activation
    3.
    发明申请
    Modified proteases that inhibit complement activation 审中-公开
    抑制补体激活的修饰蛋白酶

    公开(公告)号:US20070093443A1

    公开(公告)日:2007-04-26

    申请号:US11584776

    申请日:2006-10-20

    Abstract: Provided are methods for and compounds for modulating the complement system. In particular, compounds are provided that inhibit complement activation and compounds are provided that promote complement activation. The compounds are therapeutics by virtue of their effects on the complement system. Hence, the compounds that inhibit complement activation can be used for treatment of ischemic and reperfusion disorders, including myocardial infarction and stroke, sepsis, autoimmune diseases, inflammatory diseases and diseases with an inflammatory component, including Alzheimer's Disease and other neurodegenerative disorder.

    Abstract translation: 提供了用于调节补体系统的方法和化合物。 特别地,提供抑制补体活化的化合物,并提供促进补体活化的化合物。 这些化合物由于其对补体系统的作用而成为治疗剂。 因此,抑制补体活化的化合物可用于治疗缺血和再灌注障碍,包括心肌梗死和中风,败血症,自身免疫性疾病,炎性疾病和具有炎性成分的疾病,包括阿尔茨海默氏病和其他神经变性疾病。

    Endotheliase-1 ligands
    4.
    发明申请
    Endotheliase-1 ligands 审中-公开
    内皮酶-1配体

    公开(公告)号:US20050164945A1

    公开(公告)日:2005-07-28

    申请号:US10969719

    申请日:2004-10-20

    CPC classification number: C07K14/001 A61K38/00

    Abstract: The disclosure describes compounds that can include a peptide or Kunitz domain that binds endotheliase 1 (ET1). The compounds can be used, e.g., to reduce angiogenesis in a subject having or at risk for a neoplastic disorder, modulate the activity of an ET1-expressing cell, modulate proteolysis of a biological structure, detect endotheliase activity or protein in a sample, and detect ET1 protein in a subjects.

    Abstract translation: 本公开描述了可以包括结合内皮酶1(ET1)的肽或Kunitz结构域的化合物。 所述化合物可用于减少患有或具有肿瘤性疾病风险的受试者的血管生成,调节表达ET1的细胞的活性,调节生物结构的蛋白水解,检测样品中的内皮酶活性或蛋白质,以及 检测受试者中的ET1蛋白。

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