Imidazol derivatives having affinity for alpha 2 receptors activity
    2.
    发明申请
    Imidazol derivatives having affinity for alpha 2 receptors activity 有权
    具有对α2受体活性的亲和力的咪唑衍生物

    公开(公告)号:US20060178417A1

    公开(公告)日:2006-08-10

    申请号:US10537622

    申请日:2003-12-05

    IPC分类号: A61K31/4164 C07D233/62

    CPC分类号: C07D233/64

    摘要: Novel prodrugs of MPV-2426, methods for preparing said prodrug forms, pharmaceutical compositions containing such prodrug forms, and methods for using the prodrug forms. A compound of general formula (I), or pharmaceutically acceptable salts or hydrates thereof, wherein R represents unsubstituted or substituted lower alkyl, unsubstituted or substituted aryl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted heteroaryl, unsubstituted or substituted lower alkylamino or a saturated five or six membered heterocyclic group containing one or two nitrogen atoms.

    摘要翻译: MPV-2426的新型前药,制备所述前体药物形式的方法,含有该前药形式的药物组合物,以及使用前药形式的方法。 通式(I)的化合物或其药学上可接受的盐或水合物,其中R表示未取代或取代的低级烷基,未取代或取代的芳基,未取代或取代的环烷基,未取代或取代的杂芳基,未取代或取代的低级烷基氨基或饱和五 或含有一个或两个氮原子的六元杂环基。

    Imidazole derivatives having affinity for alpha 2 receptors activity
    4.
    发明授权
    Imidazole derivatives having affinity for alpha 2 receptors activity 有权
    对α2受体活性具有亲和力的咪唑衍生物

    公开(公告)号:US07759496B2

    公开(公告)日:2010-07-20

    申请号:US10537622

    申请日:2003-12-05

    IPC分类号: A61K31/4164 C07D233/64

    CPC分类号: C07D233/64

    摘要: Novel prodrugs of MPV-2426, methods for preparing said prodrug forms, pharmaceutical compositions containing such prodrug forms, and methods for using the prodrug forms. A compound of general formula (I), or pharmaceutically acceptable salts or hydrates thereof, wherein R represents unsubstituted or substituted lower alkyl, unsubstituted or substituted aryl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted heteroaryl, unsubstituted or substituted lower alkylamino or a saturated five or six membered heterocyclic group containing one or two nitrogen atoms.

    摘要翻译: MPV-2426的新型前药,制备所述前体药物形式的方法,含有该前药形式的药物组合物,以及使用前药形式的方法。 通式(I)的化合物或其药学上可接受的盐或水合物,其中R表示未取代或取代的低级烷基,未取代或取代的芳基,未取代或取代的环烷基,未取代或取代的杂芳基,未取代或取代的低级烷基氨基或饱和五 或含有一个或两个氮原子的六元杂环基。