4-chloro-1-(((5S,7S)-3-((2-methyltetrahydrofuran-2-yl)methyl)-2-oxo-1-oxa-3-azaspiro[4.5]decan-7-yl)methyl)-1H-benzo[d]imidazole-6-carbonitrile | 1416506-95-0

• 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: 4-chloro-1-(((5S,7S)-3-((2-methyltetrahydrofuran-2-yl)methyl)-2-oxo-1-oxa-3-azaspiro[4.5]decan-7-yl)methyl)-1H-benzo[d]imidazole-6-carbonitrile
• 英文别名: 7-chloro-3-[[(5S,7S)-3-[(2-methyloxolan-2-yl)methyl]-2-oxo-1-oxa-3-azaspiro[4.5]decan-7-yl]methyl]benzimidazole-5-carbonitrile
• CAS: 1416506-95-0
• 化学式: C₂₃H₂₇ClN₄O₃
• 分子量: 442.945
• InChiKey: VSZYLDNPRSGSDF-GDTQQENISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  31
• 可旋转键数：
  4
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  80.4
• 氢给体数：
  0
• 氢受体数：
  5

文献信息

• TRPV4 ANTAGONISTS
  申请人：GlaxoSmithKline Intellectual Property (No. 2) Limited

  公开号：EP2720697B1

  公开（公告）日：2016-07-20
• US8927585B2
  申请人：——

  公开号：US8927585B2

  公开（公告）日：2015-01-06
• [EN] TRPV4 ANTAGONISTS<br/>[FR] ANTAGONISTES DE TRPV4
  申请人：GLAXOSMITHKLINE LLC

  公开号：WO2012174340A1

  公开（公告）日：2012-12-20

  The present invention relates to spirocarbamate analogs, pharmaceutical compositions containing them and their use as TRPV4 antagonists. The TRPV4 antagonist may be administered alone or in conjunction with one or more other therapeutic agents, ego agents being selected from the group consisting of endothelin receptor antagonists, angiotensin converting enzyme (ACE) inhibitors, angiotensin II receptor antagonists, vasopeptidase inhibitors, vasopressin receptor modulators, diuretics, digoxin, beta blocker, aldosterone antagonists, iontropes, NSAIDS, nitric oxide donors, calcium channel modulators, muscarinic antagonists, steroidal anti-inflammatory drugs, bronchodilators, anti-histamines, leukotriene antagonist, HMG-CoA reductase inhibitors, dual non-selective padrenoceptor and u1 -adrenoceptor antagonists, type-5 phosphodiesterase inhibitors, and renin inhibitors.