螺[呋喃并[3,4-B]吡啶-5(7H),3’-吡咯烷]-7-酮 | 869969-57-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 中文名称: 螺[呋喃并[3,4-B]吡啶-5(7H),3’-吡咯烷]-7-酮
• 英文名称: 7H-spiro[furo[3,4-b]pyridine-5,3'-pyrrolidin]-7-one
• 英文别名: spiro[furo[3,4-b]pyridine-5,3'-pyrrolidine]-7-one
• CAS: 869969-57-3
• 化学式: C₁₀H₁₀N₂O₂
• mdl: MFCD11045518
• 分子量: 190.202
• InChiKey: OLZQAJJGHIMZCZ-UHFFFAOYSA-N

物化性质

• 沸点：
  434.5±45.0 °C(Predicted)
• 密度：
  1.37

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  51.2
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  Tert-butyl 7-oxospiro[furo[3,4-b]pyridine-5,3'-pyrrolidine]-1'-carboxylate 生成 螺[呋喃并[3,4-B]吡啶-5(7H),3’-吡咯烷]-7-酮
  参考文献：
  名称：

  Amido compounds and their use as pharmaceuticals

  摘要：

  本发明涉及11-β羟基类固醇脱氢酶1型的抑制剂、矿物皮质激素受体（MR）的拮抗剂以及其药物组合物。本发明的化合物可用于治疗与11-β羟基类固醇脱氢酶1型的表达或活性以及醛固酮过量相关的各种疾病。

  公开号：

  US20050288317A1

文献信息

• Amido compounds and their use as pharmaceuticals
  申请人：Yao Wenqing

  公开号：US20050288317A1

  公开（公告）日：2005-12-29

  The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-β hydroxyl steroid dehydrogenase type 1 and/or diseases associated with aldosterone excess.

  本发明涉及11-β羟基类固醇脱氢酶1型的抑制剂、矿物皮质激素受体（MR）的拮抗剂以及其药物组合物。本发明的化合物可用于治疗与11-β羟基类固醇脱氢酶1型的表达或活性以及醛固酮过量相关的各种疾病。
• Modulators of 11-beta hydroxyl steroid dehydrogenase type 1, pharmaceutical compositions thereof, and methods of using the same
  申请人：Li Yun-Long

  公开号：US20070213311A1

  公开（公告）日：2007-09-13

  The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1 and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-β hydroxyl steroid dehydrogenase type 1.

  本发明涉及11-β羟基类固醇脱氢酶1型的抑制剂及其药物组合物。本发明的化合物可用于治疗与11-β羟基类固醇脱氢酶1型的表达或活性相关的各种疾病。
• Amido Compounds And Their Use As Pharmaceuticals
  申请人：Yao Wenqing

  公开号：US20080255154A1

  公开（公告）日：2008-10-16

  The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-β hydroxyl steroid dehydrogenase type 1 and/or diseases associated with aldosterone excess.

  本发明涉及11-β羟基类固醇脱氢酶1型的抑制剂、矿物质皮质激素受体（MR）的拮抗剂及其制药组合物。本发明的化合物可用于治疗与11-β羟基类固醇脱氢酶1型的表达或活性有关的各种疾病和/或与醛固酮过多有关的疾病。
• INHIBITORS OF 11-BETA HYDROXYL STEROID DEHYDROGENASE TYPE I AND METHODS OF USING THE SAME
  申请人：Yao Wenqing

  公开号：US20090298808A1

  公开（公告）日：2009-12-03

  The present invention relates to inhibitors of 11-β hydroxyl steroid dehydrogenase type 1, antagonists of the mineralocorticoid receptor (MR), and pharmaceutical compositions thereof. The compounds of the invention can be useful in the treatment of various diseases associated with expression or activity of 11-β hydroxyl steroid dehydrogenase type 1 and/or diseases associated with aldosterone excess.

  本发明涉及11-β羟基类固醇脱氢酶1型的抑制剂、矿物质皮质激素受体（MR）的拮抗剂以及其制药组合物。本发明的化合物可用于治疗与11-β羟基类固醇脱氢酶1型的表达或活性相关的各种疾病，以及与醛固酮过多相关的疾病。
• AMIDO COMPOUNDS AND THEIR USE AS PHARMACEUTICALS
  申请人：Incyte Corporation

  公开号：EP1756063B1

  公开（公告）日：2015-07-08