3-[(3-Chloro-4-methoxyphenyl)methyl]-5-ethyl-2-(oxan-4-ylamino)-7,8-dihydroimidazo[2,1-b]purin-4-one

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并嘧啶类
• 英文名称: 3-[(3-Chloro-4-methoxyphenyl)methyl]-5-ethyl-2-(oxan-4-ylamino)-7,8-dihydroimidazo[2,1-b]purin-4-one
• 化学式: C₂₂H₂₇ClN₆O₃
• 分子量: 458.9
• InChiKey: SNOYPMXIWFKCFE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  32
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  84.2
• 氢给体数：
  1
• 氢受体数：
  6

文献信息

• [EN] POLYCYCLIC GUANINE PHOSPHODIESTERASE V INHIBITORS<br/>[FR] INHIBITEURS POLYCYCLIQUES DE LA PHOSPHODIESTERASE V DE LA GUANINE
  申请人：SCHERING CORP

  公开号：WO2003020724A1

  公开（公告）日：2003-03-13

  A polycyclic guanine phosphodiesterase V inhibitor having the formula (I.1) or (II.1), with the variables defined herein, which is useful for treating sexual dysfunction and other physiological disorders (I), (II), A representative example is: (III)

  一种具有公式（I.1）或（II.1）的多环鸟嘌呤磷酸二酯酶V抑制剂，其中变量在此定义，可用于治疗性功能障碍和其他生理障碍（I），（II），代表性示例为：（III）
• Organic compounds
  申请人：Fienberg Allen A.

  公开号：US10010553B2

  公开（公告）日：2018-07-03

  The present invention relates to a new use of phosphodiesterase 1 (PDE1) inhibitors for the treatment of psychosis, schizophrenia, schizoaffective disorder, schizophreniform disorder, psychotic disorder, delusional disorder, mania, or bipolar disorder.

  本发明涉及一种磷酸二酯酶1（PDE1）抑制剂的新用途，用于治疗精神病、精神分裂症、情感分裂症、精神分裂症、精神病性障碍、妄想性障碍、躁狂症或双相情感障碍。
• 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）抑制剂和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 抑制剂和 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）抑制剂和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 抑制剂和 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。
• PDE1 inhibitors for ophthalmic disorders
  申请人：Davis Robert

  公开号：US11464781B2

  公开（公告）日：2022-10-11

  Compounds that inhibit phosphodiesterase 1 (PDE1) are useful to treat glaucoma or elevated intraocular pressure. The PDE1 inhibitors may be administered as monotherapy or in combination with additional intraocular-pressure lowering agents. In addition, the invention provides ophthalmic compositions comprising PDE 1 inhibitors and optionally one or more additional intraocular pressure-lowering agents. Topical and systemic therapy may be used.

  抑制磷酸二酯酶 1 (PDE1) 的化合物可用于治疗青光眼或眼压升高。PDE1 抑制剂可作为单药或与其他降低眼压的药物联合使用。此外，本发明还提供了包含 PDE 1 抑制剂和一种或多种额外的眼压降低剂的眼科组合物。可采用局部和全身疗法。