Modified kisspeptin peptides and uses thereof
    1.
    发明授权
    Modified kisspeptin peptides and uses thereof 有权
    改良的kisspeptin肽及其用途

    公开(公告)号:US09382293B2

    公开(公告)日:2016-07-05

    申请号:US14384685

    申请日:2013-03-14

    CPC classification number: C07K7/06 A61K9/0053 A61K38/00 C07K7/64

    Abstract: The present application provides synthetic modified peptides of five to seven natural or non-natural amino acids as well as pharmaceutical compositions comprising them, for use in the treatment a disease or disorder presenting behavioral abnormalities associated with impairment of sensory gating function, depression or cognitive impairment, particularly schizophrenia and Alzheimer's disease.

    Abstract translation: 本申请提供五至七个天然或非天然氨基酸的合成修饰肽以及包含它们的药物组合物,用于治疗与感觉门控功能障​​碍,抑郁症或认知障碍相关的行为异常的疾病或病症 ,特别是精神分裂症和阿尔茨海默病。

    REVERSIBLE PEGYLATED DRUGS
    2.
    发明申请
    REVERSIBLE PEGYLATED DRUGS 有权
    可逆的PEGY药物

    公开(公告)号:US20150057219A1

    公开(公告)日:2015-02-26

    申请号:US14468672

    申请日:2014-08-26

    Abstract: Reversible pegylated drugs are provided by derivatization of free functional groups of the drug selected from amino, hydroxyl, mercapto, phosphate and/or carboxyl with groups sensitive to mild basic conditions such as 9-fluorenylmethoxycarbonyl (Fmoc) or 2-sulfo-9-fluorenylmethoxycarbonyl (FMS), to which group a PEG moiety is attached. In these pegylated drugs, the PEG moiety and the drug residue are not linked directly to each other, but rather both residues are linked to different positions of the scaffold Fmoc or FMS structure that is highly sensitive to bases and is removable under physiological conditions. The drugs are preferably drugs containing an amino group, most preferably peptides and proteins of low or medium molecular weight. Similar molecules are provided wherein a protein carrier or another polymer carrier replaces the PEG moiety.

    Abstract translation: 可逆的聚乙二醇化药物通过衍生自选自氨基,羟基,巯基,磷酸酯和/或羧基的药物的游离官能团与对温和碱性条件敏感的基团如9-芴基甲氧基羰基(Fmoc)或2-磺基-9-芴基甲氧基羰基 (FMS),连接有PEG部分的基团。 在这些聚乙二醇化药物中,PEG部分和药物残留物不直接相互连接,而是两个残基都连接到对碱基高度敏感并在生理条件下可去除的支架Fmoc或FMS结构的不同位置。 药物优选是含有氨基的药物,最优选低分子量或中等分子量的肽和蛋白质。 提供了类似的分子,其中蛋白质载体或另一种聚合物载体取代了PEG部分。

    Short beta-defensin-derived peptides
    6.
    发明授权
    Short beta-defensin-derived peptides 有权
    短的β-防御素衍生肽

    公开(公告)号:US09567371B2

    公开(公告)日:2017-02-14

    申请号:US14880238

    申请日:2015-10-11

    Abstract: The invention is directed to β-defensin-derived peptides and their use in modulating the activity of hematopoietic cells, particularly hematopoietic stem cells and progenitor cells. Specifically, the invention provides compositions and methods useful for promoting mobilization and transplantation of hematopoietic stem cells and progenitor cells. The invention further provides compositions and methods useful in the treatment of cancer.

    Abstract translation: 本发明涉及β-防御素衍生的肽及其在调节造血细胞,特别是造血干细胞和祖细胞活性中的用途。 具体地,本发明提供了有助于促进造血干细胞和祖细胞的移动和移植的组合物和方法。 本发明还提供了可用于治疗癌症的组合物和方法。

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