Piperazinyl-propyl-pyrazole derivatives as dopamine D4 receptor antagonists, and pharmaceutical compositions containing the same
    1.
    发明授权
    Piperazinyl-propyl-pyrazole derivatives as dopamine D4 receptor antagonists, and pharmaceutical compositions containing the same 有权
    哌嗪基 - 丙基 - 吡唑衍生物作为多巴胺D4受体拮抗剂,以及含有它们的药物组合物

    公开(公告)号:US08236806B2

    公开(公告)日:2012-08-07

    申请号:US12530312

    申请日:2007-07-13

    CPC分类号: C07D403/06

    摘要: The present invention relates to a novel piperazinyl-propyl-pyrazole derivative, a method of its preparation and a pharmaceutically acceptable composition comprising the same. The novel piperazinyl-propyl-pyrazole derivative of the present invention has superior selective affinity for dopamine D4 receptor, can effectively inhibit psychotic behavior (cage climbing) induced by apomorphine, and has relatively low adverse effects in mouse rotarod test. Therefore, it can be developed as a therapeutic agent for the treatment and prevention of central nervous system (CNS) disorders, in particular, schizophrenia, attention deficit hyperactivity disorder, depression, stress diseases, panic disorder, phobia, obsessive-compulsive disorder, posttraumatic stress disorder, cognitive disorder, Alzheimer's disease, Parkinson's disease, anxiety, paraphrenia, mania, seizure disorder, personality disorder, migraine, drug addiction, alcohol addiction, obesity, eating disorder, and sleeping disorder.

    摘要翻译: 本发明涉及一种新的哌嗪基 - 丙基 - 吡唑衍生物,其制备方法和包含其的药学上可接受的组合物。 本发明的新型哌嗪基 - 丙基 - 吡唑衍生物对多巴胺D4受体具有优异的选择性亲和力,可有效抑制阿扑吗啡诱导的精神病性行为(笼养),并在小鼠旋转试验中具有较低的不良反应。 因此,它可以被开发为用于治疗和预防中枢神经系统(CNS)障碍,特别是精神分裂症,注意缺陷多动障碍,抑郁症,压力疾病,恐慌症,恐惧症,强迫症,创伤后疼痛的治疗剂 压力障碍,认知障碍,阿尔茨海默病,帕金森病,焦虑症,过敏性反应,躁狂症,癫痫发作,人格障碍,偏头痛,药物成瘾,酒精成瘾,肥胖,进食障碍和睡眠障碍。

    Tetrahydropyridine derivatives acting on muscarinic acetylcholine receptors
    4.
    发明授权
    Tetrahydropyridine derivatives acting on muscarinic acetylcholine receptors 失效
    作用于毒蕈碱乙酰胆碱受体的四氢吡啶衍生物

    公开(公告)号:US06716857B2

    公开(公告)日:2004-04-06

    申请号:US10273630

    申请日:2002-10-18

    IPC分类号: A61K3144

    CPC分类号: C07D401/06

    摘要: The present invention relates to novel tetrahydropyridine derivatives of formula 1 having an appropriately substituted pyrrolidinone and oxime, wherein m is 0 or 1, n is 1 or 2, R1 is hydrogen, C1-4alkyl, C2-4 alkynyl or aryl, R3 is C1-4 alkyl, which show high efficacy, low cholinergic adverse effects and high affinity for muscarinic acetylcholine receptor; and pharmaceutically acceptable salts thereof; processes for the preparation thereof; and pharmaceutical compositions comprising these compounds or salts.

    摘要翻译: 本发明涉及具有适当取代的吡咯烷酮和肟的式1的新的四氢吡啶衍生物,其中m为0或1,n为1或2,R 1为氢,C 1-4烷基,C 2-4炔基或芳基, R 3是C 1-4烷基,其显示出高效力,低胆碱能不良反应和对毒蕈碱性乙酰胆碱受体的高亲和力; 及其药学上可接受的盐; 制备方法; 和包含这些化合物或盐的药物组合物。

    Piperazinyl-propyl-pyrazole derivatives as dopamine D4 receptor antagonists, and pharmaceutical compositions containing the same
    5.
    发明授权
    Piperazinyl-propyl-pyrazole derivatives as dopamine D4 receptor antagonists, and pharmaceutical compositions containing the same 有权
    哌嗪基 - 丙基 - 吡唑衍生物作为多巴胺D4受体拮抗剂,以及含有它们的药物组合物

    公开(公告)号:US08372844B2

    公开(公告)日:2013-02-12

    申请号:US13454817

    申请日:2012-04-24

    CPC分类号: C07D403/06

    摘要: The present invention relates to a novel piperazinyl-propyl-pyrazole derivative, a method of its preparation and a pharmaceutically acceptable composition comprising the same. The novel piperazinyl-propyl-pyrazole derivative of the present invention has superior selective affinity for dopamine D4 receptor, can effectively inhibit psychotic behavior (cage climbing) induced by apomorphine, and has relatively low adverse effects in mouse rotarod test. Therefore, it can be developed as a therapeutic agent for the treatment and prevention of central nervous system (CNS) disorders, in particular, schizophrenia, attention deficit hyperactivity disorder, depression, stress diseases, panic disorder, phobia, obsessive-compulsive disorder, posttraumatic stress disorder, cognitive disorder, Alzheimer's disease, Parkinson's disease, anxiety, paraphrenia, mania, seizure disorder, personality disorder, migraine, drug addiction, alcohol addiction, obesity, eating disorder, and sleeping disorder.

    摘要翻译: 本发明涉及一种新的哌嗪基 - 丙基 - 吡唑衍生物,其制备方法和包含其的药学上可接受的组合物。 本发明的新型哌嗪基 - 丙基 - 吡唑衍生物对多巴胺D4受体具有优异的选择性亲和力,可有效抑制阿扑吗啡诱导的精神病性行为(笼养),并在小鼠旋转试验中具有较低的不良反应。 因此,它可以被开发为用于治疗和预防中枢神经系统(CNS)障碍,特别是精神分裂症,注意缺陷多动障碍,抑郁症,压力疾病,恐慌症,恐惧症,强迫症,创伤后疼痛的治疗剂 压力障碍,认知障碍,阿尔茨海默病,帕金森病,焦虑症,过敏性反应,躁狂症,癫痫发作,人格障碍,偏头痛,药物成瘾,酒精成瘾,肥胖,进食障碍和睡眠障碍。

    Pyrrolidinone derivatives, their preparation and pharmaceutical composition comprising the same
    7.
    发明授权
    Pyrrolidinone derivatives, their preparation and pharmaceutical composition comprising the same 失效
    吡咯烷酮衍生物,其制备方法和包含它们的药物组合物

    公开(公告)号:US06759419B2

    公开(公告)日:2004-07-06

    申请号:US10273643

    申请日:2002-10-18

    IPC分类号: A61K31445

    CPC分类号: C07D413/14

    摘要: The present invention relates to substituted pyrrolidinone compounds of formula 1, wherein n is 0 or 1; Aza is a heterocycle optionally substituted with C1-4 alkyl, or C1-4 alkyl substituted with a heterocycle, which represents a saturated or unsaturated five- or six-membered ring having nitrogen(s) as a heteroatom, which are muscarinic acetylcholine receptor agonists and useful as nootropics and therapeutic agents for cerebral neural diseases such as Alzheimer's disease; and pharmaceutically acceptable salts thereof; processes for the preparation thereof; and pharmaceutical compositions comprising these compounds or salts.

    摘要翻译: 本发明涉及式1的取代吡咯烷酮化合物,其中n为0或1; 氮杂是任选被C 1-4烷基取代的杂环,或被杂环取代的C 1-4烷基,其表示饱和或不饱和的具有氮(S)杂原子的五元或六元环,它们是毒蕈碱性乙酰胆碱受体激动剂 并且可用作脑神经疾病如阿尔茨海默病的神经调节剂和治疗剂; 及其药学上可接受的盐; 制备方法; 和包含这些化合物或盐的药物组合物。