Methods and compositions useful for modulation of angiogenesis using protein kinase Raf and Ras
    1.
    发明申请
    Methods and compositions useful for modulation of angiogenesis using protein kinase Raf and Ras 审中-公开
    使用蛋白激酶Raf和Ras调节血管发生的方法和组合物

    公开(公告)号:US20060040853A1

    公开(公告)日:2006-02-23

    申请号:US11219264

    申请日:2005-09-02

    IPC分类号: A61K38/48 A61K9/127

    CPC分类号: A61K38/45 A61K48/00

    摘要: The present invention describes methods for modulating angiogenesis in tissues using Raf and/or Ras protein, modified Raf or Ras protein, and nucleic acids encoding for such. Particularly the invention describes methods for inhibiting angiogenesis using an inactive Raf and/or Ras protein, or nucleic acids encoding therefor, or for potentiating angiogenesis using an active Raf and/or Ras protein, or nucleic acids encoding therefor. The invention also describes the use of gene delivery systems for providing nucleic acids encoding for the Raf or Ras protein, or modified forms thereof.

    摘要翻译: 本发明描述了使用Raf和/或Ras蛋白,修饰的Raf或Ras蛋白调节组织中血管生成的方法,以及编码这种方法的核酸。 特别地,本发明描述了使用非活性Raf和/或Ras蛋白质或其编码的核酸抑制血管生成或使用活性Raf和/或Ras蛋白质或其编码的核酸来增强血管生成的方法。 本发明还描述了基因递送系统用于提供编码Raf或Ras蛋白质的核酸或其修饰形式的用途。

    Method of treatment of myocardial infarction
    2.
    发明申请
    Method of treatment of myocardial infarction 审中-公开
    心肌梗死的治疗方法

    公开(公告)号:US20060258686A1

    公开(公告)日:2006-11-16

    申请号:US10535325

    申请日:2003-11-18

    IPC分类号: A61K31/519

    摘要: Myocardial infarction in a mammal is treated by administering to the mammal a therapeutically effective amount of a chemical Src family tyrosine kinase protein inhibitor and the use of such inhibitor compounds for the preparation of a medicament for treating myocardial infarction. Myocardial infarction can be prevented by administering to the mammal a prophylactic amount of the inhibitor. The inhibitor preferably is an inhibitor of Src protein selected from the group consisting of a pyrazolopyrimidine class Src family tyrosine kinase inhibitor, a macrocyclic dienone class Src family tyrosine kinase inhibitor, a pyrido[2,3-d]pyrimidine class Src family tyrosine kinase inhibitor, a 4-anilino-3-quinolinecarbonitrile class Src family tyrosine kinase inhibitor, and a mixture thereof. The Src family tyrosine kinase inhibitors can be used to prepare medicaments for the treatment of myocardial infarction. Also disclosed are articles of manufacture containing a chemical Src family tyrosine kinase inhibitor.

    摘要翻译: 通过向哺乳动物施用治疗有效量的化学品Src家族酪氨酸激酶蛋白抑制剂和这种抑制剂化合物用于制备用于治疗心肌梗塞的药物的用途来治疗哺乳动物的心肌梗死。 可以通过向哺乳动物施用预防量的抑制剂来防止心肌梗死。 抑制剂优选是Src蛋白的抑制剂,其选自吡唑并嘧啶类Src家族酪氨酸激酶抑制剂,大环二烯酮类Src家族酪氨酸激酶抑制剂,吡啶并[2,3-d]嘧啶类Src家族酪氨酸激酶抑制剂 ,4-苯胺基-3-喹啉甲腈类Src家族酪氨酸激酶抑制剂及其混合物。 Src家族酪氨酸激酶抑制剂可用于制备用于治疗心肌梗死的药物。 还公开了含有化学Src家族酪氨酸激酶抑制剂的制品。

    Methods and compositions useful for inhibition of alpha v beta 5 mediated angiogenesis
    7.
    发明申请
    Methods and compositions useful for inhibition of alpha v beta 5 mediated angiogenesis 审中-公开
    用于抑制αvβ5介导的血管生成的方法和组合物

    公开(公告)号:US20060165703A1

    公开(公告)日:2006-07-27

    申请号:US11290896

    申请日:2005-11-29

    摘要: The present invention describes methods for inhibiting angiogenesis in tissues using vitronectin αvβ5 antagonists. The αvβ5-mediated angiogenesis is correlated with exposure to cytokines including vascular endothelial growth factor, transforming growth factor-α and epidermal growth factor. Inhibition of αvβ5-mediated angiogenesis is particularly preferred in vascular endothelial ocular neovascular diseases, in tumor growth and in inflammatory conditions, using therapeutic compositions containing αvβ5 antagonists.

    摘要翻译: 本发明描述了使用玻连蛋白α5β5拮抗剂抑制组织中血管生成的方法。 α-β5介导的血管发生与包括血管内皮生长因子,转化生长因子-α和表皮生长因子在内的细胞因子的暴露相关。 使用含有αV的治疗组合物,在血管内皮细胞新生血管疾病,肿瘤生长和炎性病症中,对α5β5介导的血管生成的抑制是特别优选的 5β拮抗剂。

    METHODS FOR BLOCKING CELL PROLIFERATION AND TREATING DISEASES AND CONDITIONS RESPONSIVE TO CELL GROWTH INHIBITION
    8.
    发明申请
    METHODS FOR BLOCKING CELL PROLIFERATION AND TREATING DISEASES AND CONDITIONS RESPONSIVE TO CELL GROWTH INHIBITION 审中-公开
    阻断细胞增殖和治疗细胞生长抑制的疾病和病症的方法

    公开(公告)号:US20130266636A1

    公开(公告)日:2013-10-10

    申请号:US13816218

    申请日:2011-08-12

    IPC分类号: A61K31/506

    摘要: In alternative embodiments, the invention provides methods for regulating or modulating RAF kinases. In alternative embodiments, the invention provides methods for ameliorating, preventing and/or treating diseases, infections and/or conditions having unwanted, pathological or aberrant cell proliferation, or that are responsive to inhibition or arrest of cell growth, by administration of an allosteric RAF inhibitor and/or any agent which prevents localization of RAF to mitotic spindles or mid-bodies.

    摘要翻译: 在替代实施方案中,本发明提供了调节或调节RAF激酶的方法。 在替代实施方案中,本发明提供了通过施用变构的RAF来改善,预防和/或治疗具有不想要的,病理学或异常细胞增殖或对抑制或阻止细胞生长有反应的疾病,感染和/或病症的方法 抑制剂和/或阻止RAF定位于有丝分裂心轴或中间体的任何药剂。