Imidazo pyridine derivatives which inhibit gastric acid secretion
    3.
    发明授权
    Imidazo pyridine derivatives which inhibit gastric acid secretion 失效
    抑制胃酸分泌的咪唑吡啶衍生物

    公开(公告)号:US06313136B1

    公开(公告)日:2001-11-06

    申请号:US09319890

    申请日:1999-06-14

    IPC分类号: A61K31435

    CPC分类号: C07D471/04

    摘要: The present invention relates to imidazo pyridine derivatives of the formula (I), in which the phenyl moiety is substituted, and in which the imidazo pyridine moiety is substituted with a carboxamide group in 6-position, which inhibit exogenously or endogenously stimulated gastric acid secretion and thus can be used in the prevention and treatment of gastrointestinal inflammatory diseases.

    摘要翻译: 本发明涉及式(I)的咪唑并吡啶衍生物,其中苯基部分被取代,其中咪唑并吡啶部分被6位的羧酰胺基团取代,其抑制外源或内源性刺激的胃酸分泌 因此可用于预防和治疗胃肠道炎性疾病。

    Imidazo[1,2-a]pyridine compounds
    4.
    发明授权
    Imidazo[1,2-a]pyridine compounds 有权
    咪唑并[1,2-a]吡啶化合物

    公开(公告)号:US06613775B1

    公开(公告)日:2003-09-02

    申请号:US09403510

    申请日:1999-10-22

    IPC分类号: A61K31437

    CPC分类号: C07D471/04

    摘要: The present invention relates to novel compounds, and therapeutically acceptable salts thereof of the formula (I), which inhibit exogenously or endogenously stimulated gastric acid secretion and thus can be used in the prevention and treatment of gastrointestinal inflammatory diseases.

    摘要翻译: 本发明涉及抑制外源性或内源性刺激的胃酸分泌的式(I)的新化合物及其治疗上可接受的盐,因此可用于预防和治疗胃肠炎性疾病。

    Compounds for inhibition of gastric acid secretion
    5.
    发明授权
    Compounds for inhibition of gastric acid secretion 失效
    用于抑制胃酸分泌的化合物

    公开(公告)号:US06265415B1

    公开(公告)日:2001-07-24

    申请号:US09043040

    申请日:1998-03-10

    IPC分类号: A61K31437

    CPC分类号: C07D471/04

    摘要: The present invention relates to imidazo pyridine derivatives of the formula (I), in which the phenyl moiety is substituted with lower alkyl in 2- and 6-position, which inhibit exogenously or endogenously stimulated gastric acid secretion and thus can be used in the prevention and treatment of gastrointestinal inflammatory diseases.

    摘要翻译: 本发明涉及式(I)的咪唑并吡啶衍生物,其中苯基部分被2-和6-位的低级烷基取代,其抑制外源或内源性刺激的胃酸分泌,因此可用于预防 并治疗胃肠道炎症性疾病。

    Benzyl-substituted benzimidazoles
    7.
    发明授权
    Benzyl-substituted benzimidazoles 失效
    苄基取代的苯并咪唑

    公开(公告)号:US06465505B1

    公开(公告)日:2002-10-15

    申请号:US08875132

    申请日:1997-07-17

    IPC分类号: A61K314184

    CPC分类号: A61K31/4184 C07D235/08

    摘要: The present invention relates to benzimidazole derivatives of the formula (I), in which the phenyl moiety is substituted with lower alkyl in 2- and 6-position, which inhibit exogenously or endogenously stimulated gastric acid secretion and thus can be used in the prevention and treatment of gastrointestinal inflammatory diseases.

    摘要翻译: 本发明涉及式(I)的苯并咪唑衍生物,其中苯基部分被2-和6-位的低级烷基取代,其抑制外源或内源性刺激的胃酸分泌,因此可用于预防和 治疗胃肠道炎症性疾病。