Multi-cyclic compounds and methods of use
    21.
    发明授权
    Multi-cyclic compounds and methods of use 失效
    多环化合物和使用方法

    公开(公告)号:US08236823B2

    公开(公告)日:2012-08-07

    申请号:US11977970

    申请日:2007-10-25

    IPC分类号: A61K31/4439 C07D401/04

    摘要: The present invention relates to compounds of Formulas I and II, wherein B1, B2, B3, B4, C1, C2, ring D, L1, L2 and R1-4 are defined herein, synthetic intermediates, and pharmaceutical compositions, comprising such compounds. The compounds and compositions are capable of modulating various protein kinase receptors such as Tie-2 and Aurora and, therefore, influencing kinase related disease states and conditions. The compounds, for example, are capable of treating cancer caused by unregulated angiogenesis, and inflammation as well as other proliferative disorders.

    摘要翻译: 本发明涉及式I和II的化合物,其中B1,B2,B3,B4,C1,C2,环D,L1,L2和R1-4在本文中定义,合成中间体和包含这些化合物的药物组合物。 化合物和组合物能够调节各种蛋白激酶受体如Tie-2和Aurora,因此影响激酶相关的疾病状态和状况。 该化合物例如能够治疗由不受调节的血管发生,炎症以及其它增殖性疾病引起的癌症。

    Substituted spirocyclic chromanamine compounds as Beta-Secretase modulators and methods of use
    24.
    发明授权
    Substituted spirocyclic chromanamine compounds as Beta-Secretase modulators and methods of use 有权
    取代的螺环色胺化合物作为β-分泌酶调节剂和使用方法

    公开(公告)号:US07951838B2

    公开(公告)日:2011-05-31

    申请号:US12860595

    申请日:2010-08-20

    IPC分类号: A61K31/35

    摘要: The present invention comprises a new class of compounds useful for the modulation of Beta-secretase enzyme activity and for the treatment of Beta-secretase mediated diseases, including Alzheimer's disease (AD) and related conditions. In one embodiment, the compounds have a general Formula I wherein R1, R2, R3, R4, R5, A1, A2, A3, A4, X and Z are defined herein. The invention also includes use of these compounds in pharmaceutical compositions for treatment, prophylactic or therapeutic, of disorders and conditions related to the activity of beta-secretase protein. Such disorders include, for example, Alzheimer's Disease (AD), cognitive deficits and impairment, schizophrenia and other similar central nervous system conditions. The invention also comprises further embodiments of Formula II, intermediates and processes useful for the preparation of compounds of Formulas I and II.

    摘要翻译: 本发明包括可用于调节β-分泌酶酶活性和用于治疗β-分泌酶介导的疾病(包括阿尔茨海默病(AD))和相关病症的新一类化合物。 在一个实施方案中,化合物具有通式I,其中R 1,R 2,R 3,R 4,R 5,A 1,A 2,A 3,A 4,X和Z在本文中定义。 本发明还包括在药物组合物中用于治疗,预防或治疗与β-分泌酶蛋白活性相关的病症和病症的用途。 这些疾病包括例如阿尔茨海默病(AD),认知缺陷和损伤,精神分裂症和其他类似的中枢神经系统疾病。 本发明还包括式II的其它实施方案,可用于制备式I和II化合物的中间体和方法。

    5-amino-oxazepine and 5-amino-thiazepane compounds as beta secretase antagonists and methods of use
    25.
    发明授权
    5-amino-oxazepine and 5-amino-thiazepane compounds as beta secretase antagonists and methods of use 有权
    5-氨基 - 氧氮杂和5-氨基 - 噻嗯烷化合物作为β-分泌酶拮抗剂和使用方法

    公开(公告)号:US09346827B2

    公开(公告)日:2016-05-24

    申请号:US13982222

    申请日:2012-02-06

    摘要: The present invention provides a new class of compounds useful for the modulation of beta-secretase enzyme (BACE) activity. The compounds have a general Formula (I); wherein variables A1, A3, A4, A5, A6, A8, R2, R7, X and Y of Formula (I) are defined herein. The invention also provides pharmaceutical compositions comprising the compounds, and corresponding uses of the compounds and compositions for treatment of disorders and/or conditions related to A-beta plaque formation and deposition, resulting from the biological activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits, cognitive impairments, schizophrenia and other central nervous system conditions. The invention further provides compounds of Formulas (II) and sub-formula embodiments of Formula (I) and (II), intermediates and processes and methods useful for the preparation of compounds of Formulas (I)-(II).

    摘要翻译: 本发明提供了一类可用于调节β-分泌酶(BACE)活性的化合物。 该化合物具有通式(I); 其中式(I)的变量A1,A3,A4,A5,A6,A8,R2,R7,X和Y在本文中定义。 本发明还提供包含该化合物的药物组合物,以及用于治疗由BACE的生物学活性产生的A-β斑块形成和沉积相关的病症和/或病症的化合物和组合物的相应用途。 这种BACE介导的疾病包括例如阿尔茨海默病,认知缺陷,认知障碍,精神分裂症和其他中枢神经系统疾病。 本发明进一步提供式(I)和(II)的式(II)和亚式实施方案的化合物,可用于制备式(I) - (II)化合物的中间体和方法和方法。