Use of inhibitors of the EGFR-mediated signal transduction for the treatment of benign prostatic hyperplasia (BPH) / prostatic hypertrophy
    15.
    发明申请
    Use of inhibitors of the EGFR-mediated signal transduction for the treatment of benign prostatic hyperplasia (BPH) / prostatic hypertrophy 审中-公开
    使用EGFR介导的信号转导抑制剂治疗良性前列腺增生(BPH)/前列腺肥大

    公开(公告)号:US20070099918A1

    公开(公告)日:2007-05-03

    申请号:US11609407

    申请日:2006-12-12

    IPC分类号: A61K31/5377 A61K31/517

    摘要: The present invention relates to the use of specific EGF-receptor antagonists for preparing a pharmaceutical composition for the prevention and/or treatment of benign prostatic hyperplasia and/or prostatic hypertrophy, a method for the treatment or prevention of benign prostatic hyperplasia/prostatic hypertrophy comprising administering an EGF-receptor antagonist of groups (A), (B) or (C), described herein optionally in combination with known compounds for the treatment of benign prostatic hyperplasia/prostatic hypertrophy, as well as associated pharmaceutical compositions.

    摘要翻译: 本发明涉及特异性EGF受体拮抗剂用于制备预防和/或治疗良性前列腺增生和/或前列腺肥大的药物组合物的用途,治疗或预防良性前列腺增生/前列腺肥大的方法,其包括 施用本文所述的组(A),(B)或(C)组的EGF受体拮抗剂,任选与已知化合物组合用于治疗良性前列腺增生/前列腺肥大,以及相关药物组合物。

    Prodrugs of 1-methyl-2-(4-amidinophenylaminomethyl)-benzimidazol-5-yl-carboxylic acid-(N-2-pyridyl-N-2-hydroxycarbonylethyl)-amide
    16.
    发明授权
    Prodrugs of 1-methyl-2-(4-amidinophenylaminomethyl)-benzimidazol-5-yl-carboxylic acid-(N-2-pyridyl-N-2-hydroxycarbonylethyl)-amide 有权
    1-甲基-2-(4-脒基苯基氨基甲基) - 苯并咪唑-5-基 - 羧酸 - (N-2-吡啶基-N-2-羟基羰基乙基) - 酰胺的前药

    公开(公告)号:US07189743B2

    公开(公告)日:2007-03-13

    申请号:US11056029

    申请日:2005-02-11

    IPC分类号: A61K31/44

    CPC分类号: C07D401/12

    摘要: The present invention relates to new compounds of general formula having thrombin-inhibiting activity. Exemplary are: 1-Methyl-2-[4-(N-hydroxyamidino)-phenylaminomethyl]-benzimidazol-5-yl-carboxylic acid-(N-2-pyridyl-N-2-ethoxycarbonylethyl)-amide, and 1-Methyl-2-[4-(N-methoxycarbonylamidino)-phenylaminomethyl]-benzimidazol-5-yl-carboxylic acid-(N-2-pyridyl-N-2-hydroxycarbonylethyl)-amide.

    摘要翻译: 本发明涉及具有凝血酶抑制活性的新型通式化合物。 示例性的是:1-甲基-2- [4-(N-羟基脒基) - 苯基氨基甲基] - 苯并咪唑-5-基 - 羧酸 - (N-2-吡啶基-N-2-乙氧基羰基乙基) - 酰胺和1-甲基 -2- [4-(N-甲氧基羰基脒基) - 苯基氨基甲基] - 苯并咪唑-5-基 - 羧酸 - (N-2-吡啶基-N-2-羟基羰基乙基) - 酰胺。