Heteroaromatic sulphonamide prodrugs
    6.
    发明申请
    Heteroaromatic sulphonamide prodrugs 审中-公开
    杂芳香磺酰胺前药

    公开(公告)号:US20070135399A1

    公开(公告)日:2007-06-14

    申请号:US11605482

    申请日:2006-11-29

    申请人: Ralf Wyrwa

    发明人: Ralf Wyrwa

    CPC分类号: C07J43/00

    摘要: The invention relates to sulphonamide prodrugs of the general formula I, having a heteroaromatic linker, to a process for their preparation, to pharmaceutical compositions comprising these compounds and to their use for the production of orally available medicaments. The compounds according to the invention bind to carboanhydrases and inhibit these enzymes.

    摘要翻译: 本发明涉及具有杂芳族连接体的通式I的磺酰胺前药,其制备方法,包含这些化合物的药物组合物及其用于生产口服可用药物的用途。 根据本发明的化合物与碳水解酶结合并抑制这些酶。

    Prodrugs of ERbeta-selective substances, processes for their preparation and pharmaceutical compositions comprising these compounds
    8.
    发明申请
    Prodrugs of ERbeta-selective substances, processes for their preparation and pharmaceutical compositions comprising these compounds 审中-公开
    ERbeta选择性物质的前体药物,其制备方法和包含这些化合物的药物组合物

    公开(公告)号:US20070123500A1

    公开(公告)日:2007-05-31

    申请号:US11604891

    申请日:2006-11-28

    IPC分类号: A61K31/56 C07J1/00

    CPC分类号: C07J1/00

    摘要: The present invention makes available prodrugs of 9α-substituted oestratrienes of the general formula (I) in which the group Z is bonded to the steroid, processes for their preparation, pharmaceutical compositions which comprise these compounds and use thereof. The compounds of the general formula I according to the invention do not bind to the oestrogen receptor a and/or β. They bind to carboanhydrases and inhibit these enzymes.

    摘要翻译: 本发明提供了通式(I)的9α-取代的邻三烯的前药,其中基团Z与类固醇结合,其制备方法,包含这些化合物的药物组合物及其用途。 根据本发明的通式I的化合物不结合雌激素受体a和/或β。 它们与碳水解酶结合并抑制这些酶。