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Cu(dthp)Cl2 | 1417405-65-2

中文名称
——
中文别名
——
英文名称
Cu(dthp)Cl2
英文别名
——
Cu(dthp)Cl<sub>2</sub>化学式
CAS
1417405-65-2
化学式
C11H7Cl2CuN3S2
mdl
——
分子量
379.781
InChiKey
WGKBSZDGDBJHGJ-UHFFFAOYSA-L
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:
    copper(II) choride dihydrate 、 2,6-di(thiazol-2-yl)pyridine甲醇 为溶剂, 反应 2.0h, 以68%的产率得到Cu(dthp)Cl2
    参考文献:
    名称:
    Synthesis, crystal structure, DNA interaction and anticancer activity of tridentate copper(II) complexes
    摘要:
    Three new tridentate copper(II) complexes [Cu(dthp)Cl-2] (1) (dthp = 2,6-di(thiazol-2-yl)pyridine), [Cu(dmtp)Cl-2] (2) (dmtp = 2,6-di(5-methyl-4H-1,2,4-triazol-3-yl)pyridine) and [Cu(dtp)Cl-2] (3) (dtp = 2,6-di(4H-1,2,4-triazol-3-yl)pyridine) have been synthesized and characterized. Crystal structure of complex 1 shows that the complex existed as distorted square pyramid with five co-ordination sites occupied by the tridentate ligand and the two chlorine anions. Ethidium bromide displacement assay, viscosity measurements, circular dichroism studies and cyclic voltammetric experiments suggested that these complexes bound to DNA via an intercalative mode. Three Cu(II) complexes were found to efficiently cleave DNA in the presence of sodium ascorbate, and singlet oxygen (O-1(2)) and hydrogen peroxide were proved to contribute to the DNA cleavage process. They exhibited anticancer activity against HeLa, Hep-G2 and BEL-7402 cell lines. Nuclear chromatin cleavage has also been observed with AO/EB staining assay and the alkaline single-cell gel electrophoresis (comet assay). The results demonstrated that three Cu(II) complexes cause DNA damage that can induce the apoptosis of BEL-7402 cells. (C) 2012 Elsevier Inc. All rights reserved.
    DOI:
    10.1016/j.jinorgbio.2012.09.019
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