Oxadiazolyl-phenoxyalkylisoxazoles, compositions thereof and methods for their use as anti-picornaviral agents
    4.
    发明申请
    Oxadiazolyl-phenoxyalkylisoxazoles, compositions thereof and methods for their use as anti-picornaviral agents 失效
    恶二唑基 - 苯氧基烷基异恶唑,其组合物及其用作抗小刀毒病毒剂的方法

    公开(公告)号:US20050043542A1

    公开(公告)日:2005-02-24

    申请号:US10487852

    申请日:2002-08-29

    CPC分类号: C07D413/12

    摘要: Oxadiazolyl-phenoxyalkylisoxazoles and pharmaceutically acceptable salts thereof, compositions comprising oxadiazolyl-phenoxyalkylisoxazole compounds or pharmaceutically acceptable salts thereof and methods for using oxadiazolyl-phenoxyalkylisoxazole compounds or pharmaceutically acceptable salts thereof as anti-picornaviral agents are described herein. The methods include using pleconaril as a prodrug for conversion to anti-picornaviral compounds in vivo.

    摘要翻译: 本文描述了恶二唑基 - 苯氧基烷基异恶唑及其药学上可接受的盐,其包含恶二唑基 - 苯氧基烷基异恶唑化合物或其药学上可接受的盐和使用恶二唑基 - 苯氧基烷基异恶唑化合物或其药学上可接受的盐作为抗小RNA病毒剂的方法。 所述方法包括使用pleconaril作为在体内转化成抗小刀毒蛋白病毒化合物的前药。

    Preparation of pharmaceutical salts of 3-O-(3',3'-dimethylsuccinyl)betulinic acid
    8.
    发明申请
    Preparation of pharmaceutical salts of 3-O-(3',3'-dimethylsuccinyl)betulinic acid 审中-公开
    3-O-(3',3'-二甲基琥珀酰基)桦木酸的药物盐的制备

    公开(公告)号:US20070203103A1

    公开(公告)日:2007-08-30

    申请号:US11640488

    申请日:2006-12-18

    IPC分类号: A61K31/56 C07J53/00

    CPC分类号: C07J63/008 C07J53/00

    摘要: This invention relates to a novel process for making 3-O-(3′,3′-dimethylsuccinyl)betulinic acid (“DSB”). This invention also relates to methods of treating HIV and related diseases using pharmaceutical compositions comprising salt forms of DSB prepared according to the process of the present invention. The invention further relates to dosage forms of pharmaceutical compositions comprising salts of DSB made using the process of this invention.

    摘要翻译: 本发明涉及一种制备3-O-(3',3'-二甲基琥珀酰基)桦木酸(“DSB”)的新方法。 本发明还涉及使用包含根据本发明方法制备的DSB盐形式的药物组合物来治疗HIV和相关疾病的方法。 本发明还涉及包含使用本发明方法制备的DSB盐的药物组合物的剂型。

    Oxadiazolyl-phenoxyalkylisoxazoles compositions thereof and methods for their use as anti-picornaviral agents
    9.
    发明申请
    Oxadiazolyl-phenoxyalkylisoxazoles compositions thereof and methods for their use as anti-picornaviral agents 审中-公开
    恶二唑基 - 苯氧基烷基异恶唑组合物及其作为抗小刀毒病毒剂的方法

    公开(公告)号:US20050027127A1

    公开(公告)日:2005-02-03

    申请号:US10487851

    申请日:2002-08-29

    IPC分类号: C07D413/12 C07D413/02

    CPC分类号: C07D413/12

    摘要: Oxadiazolyl-phenoxyalkylisoxazoles and pharmaceutically acceptable salts thereof, compositions comprising oxadiazolyl-phenoxyalkylisoxazole compounds or pharmaceutically acceptable salts thereof and methods for using oxadiazolyl-phenoxyalkylisoxazole compounds or pharmaceutically acceptable salts thereof as anti-picornaviral agents are described herein.

    摘要翻译: 本文描述了恶二唑基 - 苯氧基烷基异恶唑及其药学上可接受的盐,其包含恶二唑基 - 苯氧基烷基异恶唑化合物或其药学上可接受的盐和使用恶二唑基 - 苯氧基烷基异恶唑化合物或其药学上可接受的盐作为抗小RNA病毒剂的方法。