Cyclohexane-1,2'-Indene-1',2
    3.
    发明申请
    Cyclohexane-1,2'-Indene-1',2"-Imidazol Compounds and Their Use as Bace Inhibitors 有权
    环己烷-1,2'-茚-1',2“ - 咪唑化合物及其作为阻止剂的用途

    公开(公告)号:US20130345247A1

    公开(公告)日:2013-12-26

    申请号:US13916701

    申请日:2013-06-13

    摘要: Cyclohexane-1,2′-indene-1′,2″-imidazole compounds, therapeutically acceptable salts thereof, processes for preparation thereof, therapeutic uses of such compounds for treating Aβ-related pathologies such as Down's syndrome, β-amyloid angiopathy, Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration, methods of therapy using such compounds, and pharmaceutical compositions containing such compounds.

    摘要翻译: 环己烷-1,2'-茚-1',2“ - 咪唑化合物,其治疗上可接受的盐,其制备方法,这些化合物治疗Abeta相关病症如唐氏综合征,β-淀粉样血管病, 阿尔茨海默病,记忆丧失,与阿尔茨海默病相关的注意力缺陷症状,与诸如阿尔茨海默病或痴呆的疾病相关的神经变性,包括混合血管和退行性起源的痴呆,老年痴呆,老年痴呆和与帕金森病相关的痴呆,进行性核上性麻痹 或皮层基底变性,使用这些化合物的治疗方法,以及含有这些化合物的药物组合物。

    Cycloalkyl Ether Compounds and Their Use as Bace Inhibitors
    4.
    发明申请
    Cycloalkyl Ether Compounds and Their Use as Bace Inhibitors 有权
    环烷基醚化合物及其作为抑制剂的用途

    公开(公告)号:US20130345272A1

    公开(公告)日:2013-12-26

    申请号:US13916740

    申请日:2013-06-13

    摘要: Cycloalkyl ether compounds, therapeutically acceptable salts thereof, processes for preparation thereof, therapeutic uses of such compounds for treating Aβ-related pathologies such as Down's syndrome, β-amyloid angiopathy, Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration and pharmaceutical compositions containing such compounds.

    摘要翻译: 环烷基醚化合物,其治疗上可接受的盐,其制备方法,这些化合物治疗Abeta相关病症如唐氏综合征,β-淀粉样血管病,阿尔茨海默病,记忆丧失,与阿尔茨海默病相关的注意力缺陷症状,神经变性 与诸如阿尔茨海默病或痴呆的疾病相关,包括混合血管和退行性疾病的痴呆,老年痴呆,老年性痴呆和与帕金森病相关的老年痴呆,进行性核上性麻痹或皮层基底变性以及含有这些化合物的药物组合物。

    Cyclohexane-1,2'-Naphthalene-1',2
    5.
    发明申请
    Cyclohexane-1,2'-Naphthalene-1',2"-Imidazol Compounds and Their Use as Bace 有权
    环己烷-1,2'-萘-1',2“ - 咪唑化合物及其作为Bace的用途

    公开(公告)号:US20130345248A1

    公开(公告)日:2013-12-26

    申请号:US13916731

    申请日:2013-06-13

    摘要: Cyclohexane-1,2′-naphthalene-1′,2″-imidazole compounds, therapeutically acceptable salts thereof, processes for preparation thereof, therapeutic uses of such compounds for treating Aβ-related pathologies such as Down's syndrome, β-amyloid angiopathy, Alzheimer's disease, memory loss, attention deficit symptoms associated with Alzheimer's disease, neurodegeneration associated with diseases such as Alzheimer's disease or dementia including dementia of mixed vascular and degenerative origin, pre-senile dementia, senile dementia and dementia associated with Parkinson's disease, progressive supranuclear palsy or cortical basal degeneration, methods of therapy using such compounds, and pharmaceutical compositions containing such compounds.

    摘要翻译: 环己烷-1,2'-萘-1',2“ - 咪唑化合物,其治疗上可接受的盐,其制备方法,这些化合物治疗Abeta相关病症如唐氏综合征,β-淀粉样血管病, 阿尔茨海默病,记忆丧失,与阿尔茨海默病相关的注意力缺陷症状,与诸如阿尔茨海默病或痴呆的疾病相关的神经变性,包括混合血管和退行性起源的痴呆,老年痴呆,老年痴呆和与帕金森病相关的痴呆,进行性核上性麻痹 或皮层基底变性,使用这些化合物的治疗方法,以及含有这些化合物的药物组合物。

    Nobel compounds having selective inhibiting effect at gsk3
    8.
    发明申请
    Nobel compounds having selective inhibiting effect at gsk3 失效
    诺贝尔化合物在gsk3具有选择性抑制作用

    公开(公告)号:US20060116362A1

    公开(公告)日:2006-06-01

    申请号:US10539543

    申请日:2003-12-15

    CPC分类号: C07D401/12

    摘要: The present invention relates to new compounds of formula (I) wherein: Z is N and X is CH or N; Y is CONR5; P is phenyl or a 5 or 6 membered heteroaromatic ring containing one or more heteroatoms selected from N, O or S; Q is phenyl or a 5 or 6 membered aromatic heterocyclicc ring containing one or more nitrogen atoms; R is C1-6alkylNR10R11 or C1-6alkylazetidine; R10 is hydrogen, C1-6alkyl, C2-6alkenyl, C2-6alkynyl, C0-6alkylC3-6cycloalkyl, C0-6alkylaryl, C0-61alkylheteroaryl or C1-6alkylNR8R9; R11 is C1-6alkylNR8R9, C0-6alkylC3-6cycloalkyl or C0-6alkylheterocycloalkyl; as a free base or a pharmaceutically acceptable salt, solvate or solvate of salt thereof, a process for their preparation and new intermediates used therein, pharmaceutical formulations containing said therapeutically active compounds and to the use of said active compounds in therapy.

    摘要翻译: 本发明涉及新的式(I)化合物,其中:Z是N,X是CH或N; Y为CONR 5; P是苯基或含有一个或多个选自N,O或S的杂原子的5或6元杂芳环; Q是苯基或含有一个或多个氮原子的5或6元芳族杂环环; R是C 1-6烷基,R 10,或C 1-6烷基氮杂环丁烷; R 10是氢,C 1-6烷基,C 2-6 - 烯基,C 2-6 - 炔基 ,C 0-6-6烷基C 3-6环烷基,C 0-6烷基芳基,C 0-6-烷基杂芳基 或C 1-6烷基N R 8 R 9; R 11是C 1-6烷基,R 8,R 9,C 0-6, 烷基C 3-6环烷基或C 0-6-6烷基杂环烷基; 作为其盐的游离碱或其药学上可接受的盐,溶剂化物或溶剂化物,其制备方法和其中使用的新中间体,含有所述治疗活性化合物的药物制剂和所述活性化合物在治疗中的用途。