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3-(1-cyclohexyl-3-methyl-4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-N-phenylazetidine-1-carboxamide | 1025709-66-3

中文名称
——
中文别名
——
英文名称
3-(1-cyclohexyl-3-methyl-4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-N-phenylazetidine-1-carboxamide
英文别名
3-(1-cyclohexyl-3-methyl-4-oxo-5H-pyrazolo[3,4-d]pyrimidin-6-yl)-N-phenylazetidine-1-carboxamide
3-(1-cyclohexyl-3-methyl-4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-N-phenylazetidine-1-carboxamide化学式
CAS
1025709-66-3
化学式
C22H26N6O2
mdl
——
分子量
406.487
InChiKey
FOARBFAHVLXTHA-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):
    2.1
  • 重原子数:
    30
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    91.6
  • 氢给体数:
    2
  • 氢受体数:
    4

文献信息

  • Novel compounds useful for the treatment of degenerative & inflamatory diseases
    申请人:Edward Paul John
    公开号:US20090137549A1
    公开(公告)日:2009-05-28
    The present invention relates to compounds that are inhibitors of PDE1A, a phosphodiesterase that is involved in the modulation of the degradation of cartilage, joint degeneration and diseases involving such degradation and/or inflammation.
    本发明涉及抑制PDE1A的化合物,PDE1A是一种磷酸二酯酶,参与调节软骨降解、关节退化以及涉及这种降解和/或炎症的疾病。
  • Combinations of PDE1 inhibitors and NEP inhibitors and associated methods
    申请人:Intra-Cellular Therapies, Inc.
    公开号:US10285992B2
    公开(公告)日:2019-05-14
    The invention relates to the combination of inhibitors of phosphodiesterase 1 (PDE1) and inhibitors of Neprilysin (NEP) useful for the treatment of certain cardiovascular diseases or related disorders, e.g., hypertension, congestive heart disease, and post-myocardial infarction. In another embodiment, the invention relates to the combination of inhibitors of PDE1 and inhibitors of NEP for the treatment of diseases or disorders characterized by disruption of or damage to various cGMP/PKG mediated pathways in the cardiovascular system (e.g., in cardiac tissue or in arterial smooth muscle).
    本发明涉及磷酸二酯酶1(PDE1)抑制剂NEPrilysin(NEP抑制剂的组合,用于治疗某些心血管疾病或相关疾病,如高血压、充血性心脏病和心肌梗塞后。在另一个实施方案中,本发明涉及 PDE1 抑制剂NEP 抑制剂的组合,用于治疗以心血管系统(如心脏组织或动脉平滑肌)中各种 cGMP/PKG 介导的通路被破坏或损害为特征的疾病或紊乱。
  • Combinations of PDE1 inhibitors and NEP inhibitors
    申请人:INTRA-CELLULAR THERAPIES, INC.
    公开号:US11166956B2
    公开(公告)日:2021-11-09
    The invention relates to the combination of inhibitors of phosphodiesterase 1 (PDE1) and inhibitors of Neprilysin (NEP) useful for the treatment of certain cardiovascular diseases or related disorders, e.g., hypertension, congestive heart disease, and post-myocardial infarction. In another embodiment, the invention relates to the combination of inhibitors of PDE1 and inhibitors of NEP for the treatment of diseases or disorders characterized by disruption of or damage to various cGMP/PKG mediated pathways in the cardiovascular system (e.g., in cardiac tissue or in arterial smooth muscle).
    本发明涉及磷酸二酯酶1(PDE1)抑制剂NEPrilysin(NEP抑制剂的组合,用于治疗某些心血管疾病或相关疾病,如高血压、充血性心脏病和心肌梗塞后。在另一个实施方案中,本发明涉及 PDE1 抑制剂NEP 抑制剂的组合,用于治疗以心血管系统(如心脏组织或动脉平滑肌)中各种 cGMP/PKG 介导的通路被破坏或损害为特征的疾病或紊乱。
  • NOVEL COMBINATION
    申请人:Intra-Cellular Therapies, Inc.
    公开号:US20160038494A1
    公开(公告)日:2016-02-11
    The invention relates to the combination of inhibitors of phosphodiesterase 1 (PDE1) and inhibitors of Neprilysin (NEP) useful for the treatment of certain cardiovascular diseases or related disorders, e.g., hypertension, congestive heart disease, and post-myocardial infarction. In another embodiment, the invention relates to the combination of inhibitors of PDE1 and inhibitors of NEP for the treatment of diseases or disorders characterized by disruption of or damage to various cGMP/PKG mediated pathways in the cardiovascular system (e.g., in cardiac tissue or in arterial smooth muscle).
  • [EN] NOVEL COMPOUNDS USEFUL FOR THE TREATMENT OF DEGENERATIVE & INFLAMMATORY DISEASES<br/>[FR] NOUVEAUX COMPOSÉS UTILISÉS DANS LE TRAITEMENT DE MALADIES DÉGÉNÉRATIVES ET INFLAMMATOIRES
    申请人:GALAPAGOS NV
    公开号:WO2008055959A1
    公开(公告)日:2008-05-15
    [EN] The present invention relates to compounds of formula (I) that are inhibitors of PDElA, a phosphodiesterase that is involved in the modulation of the degradation of cartilage, joint degeneration and diseases involving such degradation and/or inflammation.
    [FR] La présente invention concerne des composés représentés par la formule (I), qui sont des inhibiteurs de PDElA, une phosphodiestérase associée à la modulation de la dégradation du cartilage, la dégénération des articulations et les maladies associées à une telle dégradation et/ou inflammation.
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