Spiro-amino-imidazolone and spiro-amino-dihydro-pyrimidinone compounds as beta-secretase modulators and methods of use
    3.
    发明授权
    Spiro-amino-imidazolone and spiro-amino-dihydro-pyrimidinone compounds as beta-secretase modulators and methods of use 有权
    螺 - 氨基 - 咪唑啉酮和螺 - 氨基 - 二氢 - 嘧啶酮化合物作为β-分泌酶调节剂和使用方法

    公开(公告)号:US08957083B2

    公开(公告)日:2015-02-17

    申请号:US13988745

    申请日:2011-11-18

    IPC分类号: C07D491/107 C07D491/20

    CPC分类号: C07D491/107 C07D491/20

    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, L, R2, R7, R9, W 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 plaque formation and deposition, resulting from the 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 III, sub-Formula embodiments of Formulas I, II and III, intermediates and processes and methods useful for the preparation of compounds of Formulae I-III.

    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。 化合物具有通式I:其中式I的变量A1,A3,A4,A5,A6,A8,L,R2,R7,R9,W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,以及用于治疗由于BACE的活性而导致的斑块形成和沉积相关疾病和/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。 本发明还提供式II和III的化合物,式I,II和III的次级实施方案,可用于制备式I-III化合物的中间体和方法和方法。

    Spiro-Amino-Imidazo-Fused Heterocyclic Compounds as Beta-secretase Modulators and Methods of Use
    4.
    发明申请
    Spiro-Amino-Imidazo-Fused Heterocyclic Compounds as Beta-secretase Modulators and Methods of Use 有权
    螺氨基 - 咪唑并 - 杂环化合物作为β-分泌酶调节剂和使用方法

    公开(公告)号:US20140038954A1

    公开(公告)日:2014-02-06

    申请号:US13982096

    申请日:2012-02-13

    IPC分类号: C07D491/20

    CPC分类号: C07D491/20 A61K31/353

    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, Y and Z 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 plaque formation and deposition, resulting from the activity of BACE. Such BACE mediated disorders include, for example, Alzheimer's Disease, cognitive deficits and impairments, schizophrenia and other central nervous system conditions and disorders. The invention further provides compounds of Formulas II and III, and of sub-formulas of Formulas I, II and III, intermediates and processes and methods useful for the preparation of compounds of Formulas I-III.

    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。 化合物具有通式I,其中式I的变量A1,A3,A4,A5,A6,A8,R2,R7,X,Y和Z如本文所定义。 本发明还提供包含该化合物的药物组合物,以及用于治疗由于BACE的活性而导致的斑块形成和沉积相关疾病和/或病症的化合物和组合物的相应用途。 这种BACE介导的病症包括例如阿尔茨海默病,认知缺陷和损伤,精神分裂症和其他中枢神经系统病症和障碍。 本发明还提供了式II和III的化合物和式I,II和III的分子式,可用于制备式I-III化合物的中间体和方法和方法。

    Spiro-Amino-Imidazolone and Spiro-Amino-Dihydro-Pyrimidinone Compounds as Beta-Secretase Modulators and Methods of Use
    5.
    发明申请
    Spiro-Amino-Imidazolone and Spiro-Amino-Dihydro-Pyrimidinone Compounds as Beta-Secretase Modulators and Methods of Use 有权
    螺氨基 - 咪唑啉酮和螺 - 氨基 - 二氢 - 嘧啶酮化合物作为β-分泌酶调节剂和使用方法

    公开(公告)号:US20130338177A1

    公开(公告)日:2013-12-19

    申请号:US13988745

    申请日:2011-11-18

    IPC分类号: C07D491/107 C07D491/20

    CPC分类号: C07D491/107 C07D491/20

    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, L, R2, R7, R9, W 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 plaque formation and deposition, resulting from the 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 (III), sub-Formula embodiments of Formulas (I), (II) and (III), intermediates and processes and methods useful for the preparation of compounds of Formulae (I-III).

    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。 化合物具有通式(I),其中式(I)的变量A1,A3,A4,A5,A6,A8,L,R2,R7,R9,W和Y如本文所定义。 本发明还提供包含该化合物的药物组合物,以及用于治疗由于BACE的活性而导致的斑块形成和沉积相关疾病和/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。 本发明还提供式(II)和(III)的化合物,式(I),(II)和(III)的分式实施方案,可用于制备式(I-III)化合物的中间体和方法和方法 )。

    Alkyne-substituted pyridone compounds and methods of use
    7.
    发明授权
    Alkyne-substituted pyridone compounds and methods of use 有权
    炔基取代的吡啶酮化合物和使用方法

    公开(公告)号:US07893061B2

    公开(公告)日:2011-02-22

    申请号:US11827910

    申请日:2007-07-13

    申请人: Ryan White

    发明人: Ryan White

    IPC分类号: C07D401/14 A61K31/506

    摘要: The present invention comprises a new class of compounds capable of modulating the c-kit receptor and, accordingly, useful for treatment of c-kit mediated diseases, including various inflammatory, fibrotic and/or mast cell mediated diseases such as mastocytosis. The compounds have a general Formula I wherein A1-3, R1 and R3-6 are defined herein. The invention further comprises pharmaceutical compositions, methods for treatment of c-kit mediated diseases, and intermediates and processes useful for the preparation of compounds of the invention.

    摘要翻译: 本发明包括能够调节c-kit受体的新一类化合物,因此可用于治疗c-kit介导的疾病,包括各种炎性,纤维化和/或肥大细胞介导的疾病如肥大细胞增多症。 该化合物具有通式I,其中A1-3,R1和R3-6在本文中定义。 本发明还包括药物组合物,用于治疗c-kit介导的疾病的方法,以及可用于制备本发明化合物的中间体和方法。

    Substituted pyridone compounds and methods of use
    8.
    发明授权
    Substituted pyridone compounds and methods of use 失效
    取代的吡啶酮化合物和使用方法

    公开(公告)号:US07700607B2

    公开(公告)日:2010-04-20

    申请号:US11879830

    申请日:2007-07-18

    IPC分类号: A61K31/517

    CPC分类号: C07D471/04 C07D401/04

    摘要: The present invention comprises a new class of compounds capable of modulating the c-kit receptor and, accordingly, useful for treatment of c-kit mediated diseases, including various inflammatory, fibrotic and/or mast cell mediated diseases such as mastocytosis. The compounds have a general Formula I wherein R1-6 are defined herein. The invention further comprises pharmaceutical compositions, methods for treatment of c-kit mediated diseases, and intermediates and processes useful for the preparation of compounds of the invention.

    摘要翻译: 本发明包括能够调节c-kit受体的新一类化合物,因此可用于治疗c-kit介导的疾病,包括各种炎性,纤维化和/或肥大细胞介导的疾病如肥大细胞增多症。 化合物具有通式I,其中R1-6在本文中定义。 本发明还包括药物组合物,用于治疗c-kit介导的疾病的方法,以及可用于制备本发明化合物的中间体和方法。

    SECURITY APPARATUS WITH RESET MECHANISM
    9.
    发明申请
    SECURITY APPARATUS WITH RESET MECHANISM 有权
    具有复位机制的安全装置

    公开(公告)号:US20090095034A1

    公开(公告)日:2009-04-16

    申请号:US11872394

    申请日:2007-10-15

    申请人: Ryan White John Hung

    发明人: Ryan White John Hung

    IPC分类号: E05B65/00 E05B37/02

    摘要: A security apparatus, a security system that uses the security apparatus, and a method of using the securing apparatus to secure a portable electronic device to an immovable object. The security apparatus comprises a combination locking mechanism with dials and tumblers, a body coupled to the dials, a reset device coupled to the tumblers, and a reset key configured to interact with the reset device to allow the user to reset the combination associated with the combination locking mechanism.

    摘要翻译: 一种安全装置,使用该安全装置的安全系统以及使用该固定装置将便携式电子装置固定在不可移动物体上的方法。 安全装置包括具有拨盘和翻转开关的组合锁定机构,耦合到拨盘的主体,耦合到翻转开关的复位装置以及配置成与复位装置相互作用的复位键,以允许用户重置与 组合锁定机构。