Pharmaceutical compounds
    12.
    发明申请
    Pharmaceutical compounds 有权
    药物化合物

    公开(公告)号:US20080076768A1

    公开(公告)日:2008-03-27

    申请号:US11789423

    申请日:2007-04-24

    CPC分类号: A61K31/5355 C07D495/04

    摘要: A thienopyrimidine of formula (I): and the pharmaceutically acceptable salts thereof have activity as inhibitors of PI3K with selectivity for the P110α subtype, and may be used to treat diseases and disorders arising from abnormal cell growth, function or behaviour, particularly those associated with PI3 kinase such as cancer, immune disorders, cardiovascular disease, viral infection, inflammation, metabolism/endocrine disorders and neurological disorders. Processes for synthesizing the compounds are also described.

    摘要翻译: 式(I)的噻吩并嘧啶及其药学上可接受的盐具有作为P110α亚型选择性的PI3K抑制剂的活性,并且可用于治疗由异常细胞生长,功能或行为引起的疾病和障碍,特别是与 PI3激酶如癌症,免疫疾病,心血管疾病,病毒感染,炎症,代谢/内分泌障碍和神经障碍。 还描述了合成化合物的方法。

    Materials and device incorporating phoshors
    15.
    发明授权
    Materials and device incorporating phoshors 失效
    材料和装置掺入磷光

    公开(公告)号:US5707548A

    公开(公告)日:1998-01-13

    申请号:US507331

    申请日:1995-10-06

    摘要: A storage phosphor material comprising a storage phosphor of the kind in which electrons excited by incident ionizing radiation may be trapped in stable trap sites and subsequently released by stimulation such as photostimulation, wherein the phosphor is contained within a host matrix which comprises a sol-gel glass in which the storage phosphor is incorporated as a dopant.

    摘要翻译: PCT No.PCT / GB94 / 02833 Sec。 371日期1995年10月6日 102(e)日期1995年10月6日PCT 1994年12月21日PCT PCT。 WO95 / 18176 PCT出版物 日期1995年7月6日一种存储磷光体材料,其包括这样的存储磷光体,其中由入射电离辐射激发的电子可以被捕获在稳定的捕获位点中,并随后通过诸如光刺激的刺激释放,其中磷光体包含在主体基质内 包括其中掺入存储磷光体作为掺杂剂的溶胶 - 凝胶玻璃。

    Pharmaceutical compounds
    16.
    发明授权
    Pharmaceutical compounds 有权
    药物化合物

    公开(公告)号:US08324206B2

    公开(公告)日:2012-12-04

    申请号:US12840070

    申请日:2010-07-20

    IPC分类号: A61K31/535

    CPC分类号: A61K31/5355 C07D495/04

    摘要: A thienopyrimidine of formula (I): and the pharmaceutically acceptable salts thereof have activity as inhibitors of PI3K with selectivity for the P110α subtype, and may be used to treat diseases and disorders arising from abnormal cell growth, function or behaviour, particularly those associated with PI3 kinase such as cancer, immune disorders, cardiovascular disease, viral infection, inflammation, metabolism/endocrine disorders and neurological disorders. Processes for synthesizing the compounds are also described.

    摘要翻译: 式(I)的噻吩并嘧啶及其药学上可接受的盐具有作为P110α亚型选择性的PI3K抑制剂的活性,并且可用于治疗由异常细胞生长,功能或行为引起的疾病和障碍,特别是与 PI3激酶如癌症,免疫疾病,心血管疾病,病毒感染,炎症,代谢/内分泌障碍和神经障碍。 还描述了合成化合物的方法。

    Pharmaceutical compounds
    17.
    发明授权
    Pharmaceutical compounds 有权
    药物化合物

    公开(公告)号:US07781433B2

    公开(公告)日:2010-08-24

    申请号:US11789423

    申请日:2007-04-24

    IPC分类号: A61K31/535 C07D413/14

    CPC分类号: A61K31/5355 C07D495/04

    摘要: A thienopyrimidine of formula (I): and the pharmaceutically acceptable salts thereof have activity as inhibitors of PI3K with selectivity for the P110α subtype, and may be used to treat diseases and disorders arising from abnormal cell growth, function or behaviour, particularly those associated with PI3 kinase such as cancer, immune disorders, cardiovascular disease, viral infection, inflammation, metabolism/endocrine disorders and neurological disorders. Processes for synthesizing the compounds are also described.

    摘要翻译: 式(I)的噻吩并嘧啶及其药学上可接受的盐具有作为P110α亚型选择性的PI3K抑制剂的活性,并且可用于治疗由异常细胞生长,功能或行为引起的疾病和障碍,特别是与 PI3激酶如癌症,免疫疾病,心血管疾病,病毒感染,炎症,代谢/内分泌障碍和神经障碍。 还描述了合成化合物的方法。