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4-[2-(3,4,5-三甲氧基苯基)乙烯基]喹啉 | 2859-98-5

中文名称
4-[2-(3,4,5-三甲氧基苯基)乙烯基]喹啉
中文别名
——
英文名称
4-[(E)-2-(3,4,5-Trimethoxy-phenyl)-vinyl]-quinoline
英文别名
4-(2-(3,4,5-Trimethoxyphenyl)vinyl)quinoline;4-[(E)-2-(3,4,5-trimethoxyphenyl)ethenyl]quinoline
4-[2-(3,4,5-三甲氧基苯基)乙烯基]喹啉化学式
CAS
2859-98-5
化学式
C20H19NO3
mdl
——
分子量
321.376
InChiKey
PAZAXHPAPRUCGE-CMDGGOBGSA-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:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.15
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    A new family of quinoline and quinoxaline analogues of combretastatins
    摘要:
    The 3-hydroxy-4-methoxyphenyl ring of combretastatin A-4 can be replaced by a 2-naphthyl moiety without significant loss of cytotoxicity and inhibition of tubulin polymerization potency. In this paper we show that the 6- or 7-quinolyl systems can in turn replace both cyclic moieties, keeping in the first case most of the potency as cytotoxic agent and in the second case as inhibitor of tubulin polymerization, related to the activities displayed by model compounds. (C) 2004 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2004.04.098
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文献信息

  • A new family of quinoline and quinoxaline analogues of combretastatins
    作者:Concepción Pérez-Melero、Ana B.S Maya、Benedicto del Rey、Rafael Peláez、Esther Caballero、Manuel Medarde
    DOI:10.1016/j.bmcl.2004.04.098
    日期:2004.7
    The 3-hydroxy-4-methoxyphenyl ring of combretastatin A-4 can be replaced by a 2-naphthyl moiety without significant loss of cytotoxicity and inhibition of tubulin polymerization potency. In this paper we show that the 6- or 7-quinolyl systems can in turn replace both cyclic moieties, keeping in the first case most of the potency as cytotoxic agent and in the second case as inhibitor of tubulin polymerization, related to the activities displayed by model compounds. (C) 2004 Elsevier Ltd. All rights reserved.
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