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(E)-5,6-dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzylidene}-2,3-dihydroinden-1-one | 1119280-79-3

中文名称
——
中文别名
——
英文名称
(E)-5,6-dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzylidene}-2,3-dihydroinden-1-one
英文别名
(2E)-5,6-dimethoxy-2-[[3-(piperidin-1-ylmethyl)phenyl]methylidene]-3H-inden-1-one
(E)-5,6-dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzylidene}-2,3-dihydroinden-1-one化学式
CAS
1119280-79-3
化学式
C24H27NO3
mdl
——
分子量
377.483
InChiKey
YUVGMQGHHQRBBC-UDWIEESQSA-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):
    4.4
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (E)-5,6-dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzylidene}-2,3-dihydroinden-1-one 在 5% Pd/C 、 氢气 作用下, 以 四氢呋喃 为溶剂, 反应 6.0h, 以84.4%的产率得到5,6-dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzyl}-2,3-dihydroinden-1-one
    参考文献:
    名称:
    Design, synthesis and AChE inhibitory activity of indanone and aurone derivatives
    摘要:
    A new series of indanone and aurone derivatives have been synthesized and tested for in vitro AChE inhibitory activity by modified Ellman method. Most of them exhibit AChE inhibitory activities superior to rivastigmine. Further, the most potent compound 1g was selected to evaluate the effect on the acquisition and memory impairment by mice step-down passive avoidance test. (C) 2008 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2008.03.003
  • 作为产物:
    描述:
    5,6-二甲氧基茚酮3-甲基哌啶苯甲醛氢氧化钾 作用下, 以 甲醇 为溶剂, 反应 3.0h, 以84.9%的产率得到(E)-5,6-dimethoxy-2-{3-[(piperidin-1-yl)methyl]-benzylidene}-2,3-dihydroinden-1-one
    参考文献:
    名称:
    Design, synthesis and AChE inhibitory activity of indanone and aurone derivatives
    摘要:
    A new series of indanone and aurone derivatives have been synthesized and tested for in vitro AChE inhibitory activity by modified Ellman method. Most of them exhibit AChE inhibitory activities superior to rivastigmine. Further, the most potent compound 1g was selected to evaluate the effect on the acquisition and memory impairment by mice step-down passive avoidance test. (C) 2008 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2008.03.003
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文献信息

  • Design, synthesis and AChE inhibitory activity of indanone and aurone derivatives
    作者:Rong Sheng、Yu Xu、Chunqi Hu、Jing Zhang、Xiao Lin、Jingya Li、Bo Yang、Qiaojun He、Yongzhou Hu
    DOI:10.1016/j.ejmech.2008.03.003
    日期:2009.1
    A new series of indanone and aurone derivatives have been synthesized and tested for in vitro AChE inhibitory activity by modified Ellman method. Most of them exhibit AChE inhibitory activities superior to rivastigmine. Further, the most potent compound 1g was selected to evaluate the effect on the acquisition and memory impairment by mice step-down passive avoidance test. (C) 2008 Elsevier Masson SAS. All rights reserved.
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