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μ-chlorobis(5,7-dichloro-8-hydroxyquinoline)bis(5,7-dichloro-8-oxyquinolinato)(ethanol)dinickel(II)-acetone (1/1) | 1357450-64-6

中文名称
——
中文别名
——
英文名称
μ-chlorobis(5,7-dichloro-8-hydroxyquinoline)bis(5,7-dichloro-8-oxyquinolinato)(ethanol)dinickel(II)-acetone (1/1)
英文别名
——
μ-chlorobis(5,7-dichloro-8-hydroxyquinoline)bis(5,7-dichloro-8-oxyquinolinato)(ethanol)dinickel(II)-acetone (1/1)化学式
CAS
1357450-64-6
化学式
C3H6O*C38H24Cl10N4Ni2O5
mdl
——
分子量
1146.62
InChiKey
YOMVDYAGGXLJIC-UHFFFAOYSA-J
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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为产物:
    描述:
    5,7-二氯-8-羟基喹啉 、 nickel(II) chloride hexahydrate 、 乙醇丙酮乙醇丙酮 为溶剂, 以70%的产率得到μ-chlorobis(5,7-dichloro-8-hydroxyquinoline)bis(5,7-dichloro-8-oxyquinolinato)(ethanol)dinickel(II)-acetone (1/1)
    参考文献:
    名称:
    Synthesis, crystal structure, DNA interaction and cytotoxicity of a dinuclear nickel(II) complex with 5,7-dichloro-8-hydroxylquinoline
    摘要:
    A new nickel(II) complex with 5,7-dichloro-8-hydroxylquinoline (H-ClQ), [NiCl(ClQ)(H-ClQ)(mu-Cl)Ni(ClQ)(CH3CH2OH)(H-ClQ)]center dot CH3COCH3 (1), was synthesized and characterized. In solid state, 1 is consisted of a dinuclear nickel(II) complex and one acetone solvent molecule. Two Ni(II) atoms are chelated by two bidentate 5,7-dichloro-8-hydroxylquinolines and coordinated by one terminal Cl atom or ethanol ligand and one mu-Cl in a distorted octahedral coordination environment. The ESI-MS result shows that the mu-Cl bridge is easily broken in solution to give mononuclear species (omitted as ClQ-Ni complex). The IC50 values of 1 for the inhibition of the proliferation of BEL7404, SGC7901 and MCF-7 tumor cells are 13.0 +/- 2.1, 15.9 +/- 5.3, and 29.8 +/- 9.5 mu M, respectively, which exhibit significantly enhanced cytotoxicity comparing with free H-ClQ and NiCl2. The binding properties of ClQ-Ni complex to DNA were investigated by UV-Vis, fluorescence, CD spectroscopy, viscosity and agarose gel electrophoresis. The results indicate that intercalation is the most probable binding mode for ClQ-Ni complex to DNA. The ClQ-Ni complex exhibits potent TOPO I inhibition activity at 50 mu M. (C) 2011 Elsevier B. V. All rights reserved.
    DOI:
    10.1016/j.ica.2011.10.002
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