N-Carbo-γ-phenylpropylpiperazin | 137517-43-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: N-Carbo-γ-phenylpropylpiperazin
• 英文别名: 4-(4-Phenylbutanoyl)piperazine；4-Phenyl-1-(piperazin-1-yl)butan-1-one；4-phenyl-1-piperazin-1-ylbutan-1-one
• CAS: 137517-43-2
• 化学式: C₁₄H₂₀N₂O
• mdl: MFCD10689007
• 分子量: 232.326
• InChiKey: SPXDRRAPPNTVJZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  17
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  32.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-Carbo-γ-phenylpropylpiperazin 在 lithium aluminium tetrahydride 作用下， 以 四氢呋喃 、 氯仿 为溶剂， 生成 1-benzoyl-4-(4-phenylbutyl)piperazine hydrochloride
  参考文献：
  名称：

  Novel 1-phenylpiperazine and 4-phenylpiperidine derivatives as high-affinity .sigma. ligands

  摘要：

  Sigma-receptors may represent an exciting new approach for the development of novel psychotherapeutic agents. Unfortunately, many of the commonly used sigma-ligands lack selectivity (e.g., many bind at phencyclidine or dopamine receptors) or suffer from other serious drawbacks. Recently, we described a series of 2-phenylaminoethanes that bind at sigma-receptors with high affinity and selectivity. Because there is evidence that 1-phenylpiperazines can structurally mimic the 2-phenylaminoethane moiety, we prepared a series of 1-phenylpiperazines and related analogues and incorporated structural features already shown to enhance the sigma-binding of the 2-phenylaminoethanes. Several of these derivatives bind at sigma-receptors with high affinity (K(i) = 1-10 nM) and lack appreciable affinity for phencyclidine and dopamine receptors. In as much as certain of these agents structurally resemble the high-affinity, but nonselective, sigma-ligand haloperidol, and because they bind with 10 times the affinity of haloperidol, we have apparently identified what appears to be the primary sigma-pharmacophore of that agent.

  DOI：

  10.1021/jm00116a003
• 作为产物：
  描述：

  1-tert-Butyl-4-(4-phenylbutanoyl)piperazine 在 甲苯 、 甲醇 作用下， 以 三氟乙酸 、 二氯甲烷 为溶剂， 反应 1.0h， 以to give the titled compound (1.63 g) as a colorless solid的产率得到N-Carbo-γ-phenylpropylpiperazin
  参考文献：
  名称：

  Efflux pump inhibitors

  摘要：

  描述了具有外排泵抑制剂活性的化合物。还描述了使用这种外排泵抑制剂化合物的方法以及包括这种化合物的药物组合物。

  公开号：

  US06399629B1

文献信息

• US6399629B1
  申请人：——

  公开号：US6399629B1

  公开（公告）日：2002-06-04
• [EN] EFFLUX PUMP INHIBITORS<br/>[FR] INHIBITEURS DE POMPES D'ECOULEMENT
  申请人：MICROCIDE PHARMACEUTICALS INC

  公开号：WO2000001714A1

  公开（公告）日：2000-01-13

  Compounds are described which have efflux pump inhibitor activity. Also described are methods of using such efflux pump inhibitor compounds and pharmaceutical compositions which include such compounds.
• WO2023/287740
  申请人：——

  公开号：——

  公开（公告）日：——
• Efflux pump inhibitors
  申请人：Microcide Pharmaceuticals, Inc.

  公开号：US06399629B1

  公开（公告）日：2002-06-04

  Compounds are described which have efflux pump inhibitor activity. Also described are methods of using such efflux pump inhibitor compounds and pharmaceutical compositions which include such compounds.

  描述了具有外流泵抑制剂活性的化合物。还描述了使用这种外流泵抑制剂化合物的方法以及包括这种化合物的药物组合物。
• Novel 1-phenylpiperazine and 4-phenylpiperidine derivatives as high-affinity .sigma. ligands
  作者：Richard A. Glennon、Mamoun Y. Yousif、Abd M. Ismaiel、Mahmoud B. El-Ashmawy、J. L. Herndon、James B. Fischer、Alfred C. Server、Kathleen J. Burke Howie

  DOI：10.1021/jm00116a003

  日期：1991.12

  Sigma-receptors may represent an exciting new approach for the development of novel psychotherapeutic agents. Unfortunately, many of the commonly used sigma-ligands lack selectivity (e.g., many bind at phencyclidine or dopamine receptors) or suffer from other serious drawbacks. Recently, we described a series of 2-phenylaminoethanes that bind at sigma-receptors with high affinity and selectivity. Because there is evidence that 1-phenylpiperazines can structurally mimic the 2-phenylaminoethane moiety, we prepared a series of 1-phenylpiperazines and related analogues and incorporated structural features already shown to enhance the sigma-binding of the 2-phenylaminoethanes. Several of these derivatives bind at sigma-receptors with high affinity (K(i) = 1-10 nM) and lack appreciable affinity for phencyclidine and dopamine receptors. In as much as certain of these agents structurally resemble the high-affinity, but nonselective, sigma-ligand haloperidol, and because they bind with 10 times the affinity of haloperidol, we have apparently identified what appears to be the primary sigma-pharmacophore of that agent.