METHOD, SYSTEM, AND APPARATUS FOR SCANNING AND IMPORTING DOCUMENTS
    1.
    发明申请
    METHOD, SYSTEM, AND APPARATUS FOR SCANNING AND IMPORTING DOCUMENTS 审中-公开
    用于扫描和导入文件的方法,系统和装置

    公开(公告)号:WO2010030678A1

    公开(公告)日:2010-03-18

    申请号:PCT/US2009/056375

    申请日:2009-09-09

    CPC classification number: G06F17/30011 G06Q10/10

    Abstract: A system, method, and apparatus for scanning and importing documents is disclosed. Specifically, the disclosed system provides a device for scanning documents and importing and forwarding scanned documents based on document identifiers. Documents are received and reviewed for entry into the document management system. An identifier is associated with each document based on the level of available information about the document. An identifier is assigned to each document. Each document with its assigned identifier is scanned. Documents are then imported into the document management system or forwarded to a recipient for additional review. Separator identifiers may be used to increase efficiency. Further, the system may allow certain users to use reporting functions to access information about the document management system and the recipients of documents.

    Abstract translation: 公开了一种扫描和导入文件的系统,方法和装置。 具体地,所公开的系统提供了用于扫描文档并基于文档标识符导入和转发扫描的文档的设备。 收到并审查文件以进入文件管理系统。 基于关于文档的可用信息的级别,标识符与每个文档相关联。 标识符被分配给每个文档。 扫描具有其分配标识符的每个文档。 然后将文档导入到文档管理系统中,或转发给收件人以进行其他审查。 分隔符标识符可用于提高效率。 此外,系统可以允许某些用户使用报告功能来访问关于文档管理系统和文档的接收者的信息。

    2-MORPHOLINYLPURINES AS INHIBITORS OF PI3K
    2.
    发明申请
    2-MORPHOLINYLPURINES AS INHIBITORS OF PI3K 审中-公开
    作为PI3K的抑制剂的2-吗啉基

    公开(公告)号:WO2009045174A1

    公开(公告)日:2009-04-09

    申请号:PCT/SG2008/000378

    申请日:2008-10-03

    CPC classification number: C07D473/32

    Abstract: The present invention relates to purine compounds that are useful as kinase inhibitors. More particularly, the present invention relates to purine compounds, methods for their preparation, pharmaceutical compositions containing these compounds and uses of these compounds in the treatment of proliferative disorders. These compounds may be useful as medicaments for the treatment of a number of proliferative disorders including tumours and cancers as well as other disorders or conditions related to or associated with mTOR kinases.

    Abstract translation: 本发明涉及可用作激酶抑制剂的嘌呤化合物。 更具体地,本发明涉及嘌呤化合物,其制备方法,含有这些化合物的药物组合物和这些化合物在增殖性疾病的治疗中的用途。 这些化合物可用作治疗许多增殖性疾病的药物,包括肿瘤和癌症以及与mTOR激酶相关或与之相关的其它病症或病症。

    8-SUBSTITUTED-2-MORPHOLINO PURINES FOR USE AS PI3K AND/OR MTOR INHIBITORS IN THE TREATMENT OF PROLIFERATIVE DISORDERS
    6.
    发明申请
    8-SUBSTITUTED-2-MORPHOLINO PURINES FOR USE AS PI3K AND/OR MTOR INHIBITORS IN THE TREATMENT OF PROLIFERATIVE DISORDERS 审中-公开
    用作PI3K和/或MTOR抑制剂治疗增殖性疾病的8-替代2-吗啡肽

    公开(公告)号:WO2010114494A1

    公开(公告)日:2010-10-07

    申请号:PCT/SG2010/000133

    申请日:2010-04-01

    CPC classification number: C07D473/32

    Abstract: The present invention relates to purine compounds of formula (I): that are useful as kinase inhibitors. More particularly, the present invention relates to purine compounds, methods for their preparation, pharmaceutical compositions containing these compounds and uses of these compounds in the treatment of proliferative disorders. These compounds may be useful as medicaments for the treatment of a number of proliferative disorders including tumours and cancers as well as other disorders or conditions related to or associated with mTOR kinases.

    Abstract translation: 本发明涉及式(I)的嘌呤化合物:其可用作激酶抑制剂。 更具体地,本发明涉及嘌呤化合物,其制备方法,含有这些化合物的药物组合物和这些化合物在增殖性疾病的治疗中的用途。 这些化合物可用作治疗许多增殖性疾病的药物,包括肿瘤和癌症以及与mTOR激酶相关或与之相关的其它病症或病症。

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