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[1-(4-Methoxynaphthalen-1-yl)sulfonyl-2,3-dihydroindol-3-yl]-[4-(3-methoxyphenyl)piperazin-1-yl]methanone | 583814-78-2

中文名称
——
中文别名
——
英文名称
[1-(4-Methoxynaphthalen-1-yl)sulfonyl-2,3-dihydroindol-3-yl]-[4-(3-methoxyphenyl)piperazin-1-yl]methanone
英文别名
——
[1-(4-Methoxynaphthalen-1-yl)sulfonyl-2,3-dihydroindol-3-yl]-[4-(3-methoxyphenyl)piperazin-1-yl]methanone化学式
CAS
583814-78-2
化学式
C31H31N3O5S
mdl
——
分子量
557.67
InChiKey
FVRZWGAORLIRIZ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    40
  • 可旋转键数:
    6
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    87.8
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    1-(4-methoxynaphthalene-1-sulfonyl)-2,3-dihydro-1H-indole-3-carboxylic Acid 、 1-(3-甲氧基苯基)哌嗪N,N-二异丙基乙胺 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下, 生成 [1-(4-Methoxynaphthalen-1-yl)sulfonyl-2,3-dihydroindol-3-yl]-[4-(3-methoxyphenyl)piperazin-1-yl]methanone
    参考文献:
    名称:
    The discovery and SAR of indoline-3-carboxamides—A new series of 5-HT6 antagonists
    摘要:
    Antagonists of the 5-HT6 receptor have been shown to improve cognitive function in a wide range of animal models and as such may prove to be attractive agents for the symptomatic treatment of cognitive disorders such as Alzheimer's disease ( AD) and schizophrenia. We report herein the identification and SAR around N-(2-aminoalkyl)-1-(arylsulfonyl)indoline-3-carboxamides-a novel chemotype of 5-HT6 antagonists. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.04.085
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文献信息

  • The discovery and SAR of indoline-3-carboxamides—A new series of 5-HT6 antagonists
    作者:Mark Reid、Ian Carlyle、Wilson L. Caulfield、Tom R. Clarkson、Fiona Cusick、Ola Epemolu、Robert Gilfillan、Richard Goodwin、David Jaap、Elise C. O’Donnell、Jeremy Presland、Zoran Rankovic、Daniel Spinks、Gayle Spinks、Anne M. Thomson、Fiona Thomson、James Strain、Grant Wishart
    DOI:10.1016/j.bmcl.2010.04.085
    日期:2010.6
    Antagonists of the 5-HT6 receptor have been shown to improve cognitive function in a wide range of animal models and as such may prove to be attractive agents for the symptomatic treatment of cognitive disorders such as Alzheimer's disease ( AD) and schizophrenia. We report herein the identification and SAR around N-(2-aminoalkyl)-1-(arylsulfonyl)indoline-3-carboxamides-a novel chemotype of 5-HT6 antagonists. (C) 2010 Elsevier Ltd. All rights reserved.
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