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6-(2-(4-methylpiperidin-1-yl))ethyl-6H-indolo[2,3-b]quinoxaline | 1216689-55-2

中文名称
——
中文别名
——
英文名称
6-(2-(4-methylpiperidin-1-yl))ethyl-6H-indolo[2,3-b]quinoxaline
英文别名
6-[2-(4-Methylpiperidin-1-yl)ethyl]indolo[3,2-b]quinoxaline
6-(2-(4-methylpiperidin-1-yl))ethyl-6H-indolo[2,3-b]quinoxaline化学式
CAS
1216689-55-2
化学式
C22H24N4
mdl
——
分子量
344.459
InChiKey
HXMLCNLSHQJYPL-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
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    34
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 作为产物:
    描述:
    4-甲基哌啶6-(2-bromoethyl)-6H-indolo[2,3-b]quinoxaline 为溶剂, 以80%的产率得到6-(2-(4-methylpiperidin-1-yl))ethyl-6H-indolo[2,3-b]quinoxaline
    参考文献:
    名称:
    Synthesis, cytotoxicity, antiviral activity and interferon inducing ability of 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines
    摘要:
    New 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines were synthesized with high yields using bromoethylisatin and 6-(2-bromoethyl)-6H-indolo[2,3-b]quinoxaline as intermediates. These compounds were screened for the cytotoxicity, antiviral activity and interferon inducing ability. it was shown, that tested 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines are low toxic potent interferon inducers and antivirals. Morpholine and 4-methyl-piperidine derivatives appeared as the most active antivirals and the least cytotoxic in the investigated series. (C) 2009 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2009.12.014
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文献信息

  • Synthesis, cytotoxicity, antiviral activity and interferon inducing ability of 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines
    作者:Marina O. Shibinskaya、Sergey A. Lyakhov、Alexander V. Mazepa、Sergey A. Andronati、Alexander V. Turov、Nadezhda M. Zholobak、Nikolay Ya. Spivak
    DOI:10.1016/j.ejmech.2009.12.014
    日期:2010.3
    New 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines were synthesized with high yields using bromoethylisatin and 6-(2-bromoethyl)-6H-indolo[2,3-b]quinoxaline as intermediates. These compounds were screened for the cytotoxicity, antiviral activity and interferon inducing ability. it was shown, that tested 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines are low toxic potent interferon inducers and antivirals. Morpholine and 4-methyl-piperidine derivatives appeared as the most active antivirals and the least cytotoxic in the investigated series. (C) 2009 Elsevier Masson SAS. All rights reserved.
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