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3-cyclohexyl-6-[5-fluoro-2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one | 553669-51-5

中文名称
——
中文别名
——
英文名称
3-cyclohexyl-6-[5-fluoro-2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one
英文别名
3-cyclohexyl-6-[5-fluoro-2-methoxy-4-(4-methylpiperazin-1-yl)phenyl]-1-methyl-5H-pyrazolo[3,4-d]pyrimidin-4-one
3-cyclohexyl-6-[5-fluoro-2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one化学式
CAS
553669-51-5
化学式
C24H31FN6O2
mdl
——
分子量
454.548
InChiKey
GBDISAUBVPINOJ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.2
  • 重原子数:
    33
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    75
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    3-Cycloheptyl-6-[5-fluoro-2-methoxy-4-(1-piperazinyl)phenyl]-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one 、 聚合甲醛甲酸碳酸氢钠 作用下, 以 乙醇 为溶剂, 反应 4.0h, 以55%的产率得到3-cyclohexyl-6-[5-fluoro-2-methoxy-4-(4-methyl-1-piperazinyl)phenyl]-1-methyl-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one
    参考文献:
    名称:
    PYRAZOLOPYRIMIDINONE DERIVATIVES HAVING PDE7-INHIBITORY ACTIVITY
    摘要:
    公开号:
    EP1454897B1
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文献信息

  • Pyrazolopyrimidinone derivatives having PDE7 inhibiting action
    申请人:Inoue Hidekazu
    公开号:US20050148604A1
    公开(公告)日:2005-07-07
    Pyrazolopyrimidinone derivatives expressed by the following general formula (IA) or (IB): and the following general formula (IA′) or (IB′): where the symbols are as disclosed in the specification, are provided as desired compounds. These compounds have the action of selectively inhibiting PDE7, thereby increasing the intracellular cAMP level and inhibiting the activation of T cells. Thus, they are useful for prevention and treatment of various allergic diseases and inflammatory or immunological diseases.
    本发明提供了以下通式(IA)或(IB)所表达的吡唑嘧啶酮衍生物,以及以下通式(IA′)或(IB′)所表达的吡唑嘧啶酮衍生物:其中所述符号如本说明书所披露的那样,作为所需的化合物提供。这些化合物具有选择性地抑制PDE7的作用,从而增加细胞内cAMP平并抑制T细胞的活化。因此,它们对于预防和治疗各种过敏性疾病和炎症或免疫性疾病是有用的。
  • Treatment of Addiction and Impulse-Control Disorders Using PDE7 Inhibitors
    申请人:OMEROS CORPORATION
    公开号:US20130267502A1
    公开(公告)日:2013-10-10
    This disclosure is directed to treatment of addictions and primary impulse-control disorders using phosphodiesterase 7 (PDE7) inhibitors, alone or in combination with other therapeutic agents.
    本公开涉及使用磷酸二酯酶7(PDE7)抑制剂,单独或与其他治疗药物联合治疗成瘾和原发性冲动控制障碍。
  • USE OF PDE7 INHIBITORS FOR THE TREATMENT OF MOVEMENT DISORDERS
    申请人:Omeros Corporation
    公开号:US20160015715A1
    公开(公告)日:2016-01-21
    A method of treating a movement abnormality associated with the pathology of a neurological movement disorder, such as Parkinson's disease or Restless Leg(s) Syndrome by administering a therapeutically effective amount of a PDE7 inhibitory agent. An aspect of the invention provides for the administration of a PDE& inhibitory agent in conjunction with a dopamine agonist or precursor, such as levodopa. In another aspect of the invention, the PDE7 inhibitory agent may be selective for PDE7 relative to other molecular targets (i) known to be involved with the pathology of Parkinson's disease or (ii) at which other drug(s) that are therapeutically effective to treat Parkinson's disease act.
    本发明涉及一种治疗神经运动障碍病理学相关的运动异常的方法,例如帕森病或不宁腿综合症,通过给予治疗有效量的PDE7抑制剂。本发明的一个方面提供了与多巴胺激动剂或前体(例如左旋多巴)一起给予PDE7抑制剂的治疗方法。在本发明的另一个方面,PDE7抑制剂可以选择性地作用于PDE7,而相对于其他分子靶点(i)已知与帕森病的病理学有关或(ii)其他治疗帕森病的药物作用的靶点。
  • PYRAZOLOPYRIMIDINONE DERIVATIVES HAVING PDE7−INHIBITORY ACTIVITY
    申请人:Daiichi Suntory Pharma Co., Ltd.
    公开号:EP1454897A1
    公开(公告)日:2004-09-08
    Pyrazolopyrimidinone derivatives expressed by the following general formula (IA) or (IB): and the following general formula (IA') or (IB'): where the symbols are as disclosed in the specification, are provided as desired compounds. These compounds have the action of selectively inhibiting PDE7, thereby increasing the intracellular cAMP level and inhibiting the activation of T cells. Thus, they are useful for prevention and treatment of various allergic diseases and inflammatory or immunological diseases.
    由以下通式(IA)或(IB)表示的吡唑嘧啶酮衍生物: 和以下通式(IA')或(IB')表示的吡唑嘧啶酮衍生物: 其中的符号如说明书中所披露的,作为所需的化合物提供。 这些化合物具有选择性抑制 PDE7 的作用,从而提高细胞内 cAMP 平并抑制 T 细胞的活化。因此,它们可用于预防和治疗各种过敏性疾病和炎症性或免疫性疾病。
  • Treatment of addiction and impulse-control disorders using PDE7 inhibitors
    申请人:Omeros Corporation
    公开号:US11207275B2
    公开(公告)日:2021-12-28
    This disclosure is directed to treatment of addictions and primary impulse-control disorders using phosphodiesterase 7 (PDE7) inhibitors, alone or in combination with other therapeutic agents.
    本公开内容涉及使用磷酸二酯酶 7 (PDE7) 抑制剂单独或与其他治疗剂联合治疗成瘾症和原发性冲动控制障碍。
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