N-[3-spiro(2,3-dihydro-1H-indene-1,4''-piperidine)ylpropyl]-1,1''-biphenyl-2-carboxyamide | 475151-94-1

• 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: N-[3-spiro(2,3-dihydro-1H-indene-1,4''-piperidine)ylpropyl]-1,1''-biphenyl-2-carboxyamide
• 英文别名: 2-phenyl-N-(3-spiro[1,2-dihydroindene-3,4'-piperidine]-1'-ylpropyl)benzamide
• CAS: 475151-94-1
• 化学式: C₂₉H₃₂N₂O
• 分子量: 424.586
• InChiKey: MYGHRPCNCRNXCV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6
• 重原子数：
  32
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.34
• 拓扑面积：
  32.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  螺[茚-1,4-哌啶] 在 palladium dihydroxide 氢气 、 potassium carbonate 、 1-羟基苯并三唑 、 一水合肼 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下， 以 四氢呋喃 、 甲醇 、 乙醇 、 氯仿 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.58h， 生成 N-[3-spiro(2,3-dihydro-1H-indene-1,4''-piperidine)ylpropyl]-1,1''-biphenyl-2-carboxyamide
  参考文献：
  名称：

  Identification of a Novel Spiropiperidine Opioid Receptor-like 1 Antagonist Class by a Focused Library Approach Featuring 3D-Pharmacophore Similarity

  摘要：

  A focused library approach identifying novel leads to develop a potent ORL1 antagonist is described. Beginning from a compound identified by random screening, an exploratory library that exhibited a diverse display of pharmacophores was designed. After evaluating ORL1 antagonistic activity, a highly focused library was designed based on 3D-pharmacophore similarity to known actives. A novel D-proline amide class was identified in this library and was found to possess potent ORL1 antagonistic activity.

  DOI：

  10.1021/jm0509851

文献信息

• Identification of a Novel Spiropiperidine Opioid Receptor-like 1 Antagonist Class by a Focused Library Approach Featuring 3D-Pharmacophore Similarity
  作者：Yasuhiro Goto、Sachie Arai-Otsuki、Yukari Tachibana、Daisuke Ichikawa、Satoshi Ozaki、Hiroyuki Takahashi、Yoshikazu Iwasawa、Osamu Okamoto、Shoki Okuda、Hisashi Ohta、Takeshi Sagara

  DOI：10.1021/jm0509851

  日期：2006.2.1

  A focused library approach identifying novel leads to develop a potent ORL1 antagonist is described. Beginning from a compound identified by random screening, an exploratory library that exhibited a diverse display of pharmacophores was designed. After evaluating ORL1 antagonistic activity, a highly focused library was designed based on 3D-pharmacophore similarity to known actives. A novel D-proline amide class was identified in this library and was found to possess potent ORL1 antagonistic activity.