4-({[5-(3-{[4-({[(2R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl]amino}methyl)-2-methylphenyl]carbamoyl}propyl)-2-phenylphenyl]carbamoyl}oxy)-1,1-dimethylpiperidin-1-ium trifluoroacetate | 1254098-02-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-({[5-(3-{[4-({[(2R)-2-hydroxy-2-(8-hydroxy-2-oxo-1,2-dihydroquinolin-5-yl)ethyl]amino}methyl)-2-methylphenyl]carbamoyl}propyl)-2-phenylphenyl]carbamoyl}oxy)-1,1-dimethylpiperidin-1-ium trifluoroacetate
• 英文别名: (1,1-dimethylpiperidin-1-ium-4-yl) N-[5-[4-[4-[[[(2R)-2-hydroxy-2-(8-hydroxy-2-oxo-1H-quinolin-5-yl)ethyl]amino]methyl]-2-methylanilino]-4-oxobutyl]-2-phenylphenyl]carbamate;2,2,2-trifluoroacetate
• CAS: 1254098-02-6
• 化学式: C₂F₃O₂*C₄₃H₅₀N₅O₆
• 分子量: 845.916
• InChiKey: UBBMXFCPXHSFOW-UFUJWDBKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.08
• 重原子数：
  61
• 可旋转键数：
  14
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  189
• 氢给体数：
  6
• 氢受体数：
  12

文献信息

• QUATERNARY AMMONIUM SALT COMPOUNDS
  申请人：Mitsuyama Etsuko

  公开号：US20120046467A1

  公开（公告）日：2012-02-23

  [Problem] The object of the present invention is to provide a novel compound having 132 adrenergic receptor agonist activity and muscarinic receptor antagonist activity. [Means for Solving the Problem] The present invention is a quaternary ammonium salt compounds represented by formula (I), or a pharmaceutically acceptable salt thereof, with superior β32 adrenergic receptor agonist activity and muscarinic receptor antagonist activity.

  本发明的目的是提供一种具有132肾上腺素受体激动剂活性和肌制剂受体拮抗活性的新型化合物。本发明是一种由化学式(I)表示的季铵盐化合物，或其在药学上可接受的盐，具有优越的β32肾上腺素受体激动剂活性和肌制受体拮抗活性。
• QUATERNARY AMMONIUM SALT COMPOUND
  申请人：Teijin Pharma Limited

  公开号：EP2426121A1

  公开（公告）日：2012-03-07

  [Problem] The abject of the present invention is to provide a novel compound having β2 adrenergic receptor agonist activity and muscarinic receptor antagonist activity. [Means for Salving the Problem The present invention is a quaternary ammonium salt compounds represented by formula (I), or a pharmaceutically acceptable salt thereof, with superior β2 adrenergic receptor agonist activity and muscarinic receptor antagonist activity.

  问题 本发明的目的是提供一种具有β2肾上腺素能受体激动剂活性和毒蕈碱受体拮抗剂活性的新型化合物。 [解决问题的方法 本发明是一种由式（I）代表的季铵盐化合物或其药学上可接受的盐，具有优异的 β2肾上腺素能受体激动剂活性和毒蕈碱受体拮抗剂活性。
• US9072734B2
  申请人：——

  公开号：US9072734B2

  公开（公告）日：2015-07-07