Sulfonamide and sulfamide substituted imidazoquinolines
    97.
    发明授权
    Sulfonamide and sulfamide substituted imidazoquinolines 有权
    磺酰胺和磺酰胺取代的咪唑并喹啉

    公开(公告)号:US06924293B2

    公开(公告)日:2005-08-02

    申请号:US10669051

    申请日:2003-09-23

    CPC classification number: A61K31/4745 C07D471/04 Y02A50/409

    Abstract: Imidazoquinoline and tetrahydroimidazoquinoline compounds that contain sulfonamide or sulfonamide functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of various cytokines and are useful in the treatment of a variety of conditions including viral diseases and neoplastic diseases.

    Abstract translation: 在1位含有磺酰胺或磺酰胺官能团的咪唑并喹啉和四氢咪唑并喹啉化合物可用作免疫反应调节剂。 本发明的化合物和组合物可以诱导各种细胞因子的生物合成,并且可用于治疗各种病症,包括病毒性疾病和肿瘤性疾病。

    Imidazonaphthyridines
    98.
    发明授权
    Imidazonaphthyridines 失效
    咪唑并萘啶

    公开(公告)号:US06747040B2

    公开(公告)日:2004-06-08

    申请号:US10405321

    申请日:2003-04-02

    Abstract: Imidazonaphthyridine compounds that are unsubstituted at the 2-position induce the biosynthesis of cytokines such as interferon and tumor necrosis factor. The compounds exhibit antiviral and antitumor properties. Methods of preparing the compounds and intermediates useful in the preparation of the compounds are also disclosed.

    Abstract translation: 在2-位未被取代的咪唑并萘啶化合物诱导细胞因子如干扰素和肿瘤坏死因子的生物合成。 该化合物显示抗病毒和抗肿瘤性质。 还公开了制备可用于制备化合物的化合物和中间体的方法。

    Process for imidazo[4,5-c]pyridin-4-amines
    99.
    发明授权
    Process for imidazo[4,5-c]pyridin-4-amines 失效
    咪唑并[4,5-c]吡啶-4-胺的方法

    公开(公告)号:US06743920B2

    公开(公告)日:2004-06-01

    申请号:US10436488

    申请日:2003-05-12

    CPC classification number: C07D471/04

    Abstract: A process and intermediates for preparing 1H-imidazo[4,5-c]pyridin-4-amines are disclosed. The process includes providing a 4-phenoxy-1H-imidazo[4,5-c]pyridine and aminating the 4-phenoxy-1H-imidazo[4,5-c]pyridine to provide a 1H-imidazo[4,5-c]pyridin-4-amine.

    Abstract translation: 公开了制备1H-咪唑并[4,5-c]吡啶-4-胺的方法和中间体。 该方法包括提供4-苯氧基-1H-咪唑并[4,5-c]吡啶并胺化4-苯氧基-1H-咪唑并[4,5-c]吡啶,得到1H-咪唑并[4,5-c ]吡啶-4-胺。

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