1-Propan-2-yl-6-oxa-1-azaspiro[3.3]heptane

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氧杂环丁烷
• 英文名称: 1-Propan-2-yl-6-oxa-1-azaspiro[3.3]heptane
• 英文别名: 1-propan-2-yl-6-oxa-1-azaspiro[3.3]heptane
• 化学式: C₈H₁₅NO
• 分子量: 141.21
• InChiKey: IQLBDAJAQRLCSD-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  12.5
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• FUSED HETEROCYCLIC COMPOUNDS AS CAM KINASE INHIBITORS
  申请人：Gilead Sciences, Inc.

  公开号：US20180148457A1

  公开（公告）日：2018-05-31

  The present disclosure relates to compounds that are CaM Kinase inhibitors and to their use in the treatment of various disease states, including atrial fibrillation and myocardial infarction. In particular embodiments, the general structure of the compounds is given by Formula I: wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 9 and R 10 are as described herein, to methods for the preparation and use of the compounds and to pharmaceutical compositions containing the same.

  本公开涉及的化合物是CaM激酶抑制剂，用于治疗各种疾病状态，包括心房颤动和心肌梗死。在特定实施例中，化合物的一般结构由公式I给出：其中R1、R2、R3、R4、R5、R6、R9和R10如本文所述，涉及化合物的制备和使用方法以及含有相同化合物的药物组合物。
• THERAPEUTIC COMPOUNDS AND USES THEREOF
  申请人：Kala Pharmaceuticals, Inc.

  公开号：US20140235657A1

  公开（公告）日：2014-08-21

  Described herein are compounds of Formula (I)-(III), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Also provided are particles (e.g., nanoparticles) comprising compounds of Formula (I)-(III) and pharmaceutical compositions thereof that are mucus penetrating. Methods of using the compounds or pharmaceutical compositions thereof for treating and/or preventing diseases are also provided.

  本文描述了公式(I)-(III)的化合物，其药学上可接受的盐以及其制药组合物。还提供了包含公式(I)-(III)化合物和制药组合物的颗粒（例如，纳米颗粒），这些颗粒具有穿透黏液的特性。还提供了使用这些化合物或制药组合物治疗和/或预防疾病的方法。
• PYRAZOLE COMPOUNDS AS MODULATORS OF FSHR AND USES THEREOF
  申请人：YU Henry

  公开号：US20160152626A1

  公开（公告）日：2016-06-02

  The present invention relates to pyrazole compounds, and pharmaceutically acceptable compositions thereof, useful as positive allosteric modulators of follicle stimulating hormone receptor (FSHR).

  本发明涉及吡唑化合物及其药学上可接受的组合物，作为卵泡刺激素受体（FSHR）的正向变构调节剂。
• Pyridazinone compounds and uses thereof
  申请人：Edgewise Therapeutics, Inc.

  公开号：US11236065B2

  公开（公告）日：2022-02-01

  Substituted pyridazinone compounds, conjugates, and pharmaceutical compositions for use in the treatment of neuromuscular diseases, such as Duchenne Muscular Dystrophy (DMD), are disclosed herein. The disclosed compounds are useful, among other things, in the treating of DMD and modulating inflammatory inhibitors IL-1, IL-6 or TNF-α.

  本文公开了用于治疗神经肌肉疾病（如杜氏肌肉萎缩症（DMD））的取代哒嗪酮化合物、共轭物和药物组合物。所公开的化合物除其他外，可用于治疗 DMD 和调节炎症抑制剂 IL-1、IL-6 或 TNF-α。
• PYRIDAZINONE COMPOUNDS AND USES THEREOF
  申请人：Edgewise Therapeutics, Inc.

  公开号：US20210179579A1

  公开（公告）日：2021-06-17

  Substituted pyridazinone compounds, conjugates, and pharmaceutical compositions for use in the treatment of neuromuscular diseases, such as Duchenne Muscular Dystrophy (DMD), are disclosed herein. The disclosed compounds are useful, among other things, in the treating of DMD and modulating inflammatory inhibitors IL-1, IL-6 or TNF-α.