Antagonistic analogs of gh rh (2003)
    3.
    发明申请
    Antagonistic analogs of gh rh (2003) 失效
    gh rh的拮抗类似物(2003)

    公开(公告)号:US20070042950A1

    公开(公告)日:2007-02-22

    申请号:US10566776

    申请日:2004-07-26

    IPC分类号: A61K38/16 C07K14/47

    CPC分类号: C07K14/60 A61K38/00

    摘要: There is provided a novel series of synthetic antagonistic analogs of hGH-RH(1-29)NH2. These analogs inhibit the activity of endogenous hGH-RH on the pituitary GH-RH receptors, and therefore prevent the release of growth hormone. The analogs also inhibit the proliferation of human cancers through a direct effect on the cancer cells. The higher inhibitory potencies of the new analogs, as compared to previously described ones, results from replacement of various amino acids.

    摘要翻译: 提供了一系列hGH-RH(1-29)NH 2的合成拮抗类似物。 这些类似物抑制内源性hGH-RH对垂体GH-RH受体的活性,因此防止生长激素的释放。 类似物还通过对癌细胞的直接作用来抑制人类癌症的增殖。 与之前描述的相比,新类似物的更高的抑制效力来自各种氨基酸的替换。

    Fluorinated GHRH antagonists
    5.
    发明授权
    Fluorinated GHRH antagonists 有权
    氟化GHRH拮抗剂

    公开(公告)号:US08227405B2

    公开(公告)日:2012-07-24

    申请号:US12562096

    申请日:2009-09-17

    IPC分类号: A61K38/16

    CPC分类号: C07K14/60 A61K38/00

    摘要: Novel fluorinated synthetic analogs of hGH-RH(1-30)NH2 that inhibit the release of growth hormone from the pituitary in mammals as well as inhibit the proliferation of human cancers through a direct effect on the cancer cells, and to therapeutic compositions containing these novel peptides and their use.

    摘要翻译: hGH-RH(1-30)NH2的新型氟化合成类似物,其抑制哺乳动物垂体中生长激素的释放,并且通过对癌细胞的直接作用抑制人类癌症的增殖,以及含有这些的治疗组合物 新型肽及其用途。