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2-(2',3-dibromo-4-formyl-phenyl)imidazo[4,5-f][1,10]-phenanthroline

中文名称
——
中文别名
——
英文名称
2-(2',3-dibromo-4-formyl-phenyl)imidazo[4,5-f][1,10]-phenanthroline
英文别名
fmp-2Br;2,5-dibromo-4-(1H-imidazo[4,5-f][1,10]phenanthrolin-2-yl)benzaldehyde
2-(2',3-dibromo-4-formyl-phenyl)imidazo[4,5-f][1,10]-phenanthroline化学式
CAS
——
化学式
C20H10Br2N4O
mdl
——
分子量
482.134
InChiKey
DLRBCWQLAXWXGC-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):
    4.5
  • 重原子数:
    27
  • 可旋转键数:
    2
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    71.5
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    2-(2',3-dibromo-4-formyl-phenyl)imidazo[4,5-f][1,10]-phenanthroline 、 ammonium hexafluorophosphate 、 以 甲醇二氯甲烷 为溶剂, 生成
    参考文献:
    名称:
    Design, synthesis and biological evaluation of liposome entrapped iridium(III) complexes toward SGC-7901 cells
    摘要:
    DOI:
    10.1016/j.jinorgbio.2023.112134
  • 作为产物:
    描述:
    1,10-邻二氮杂菲-5,6-二酮2,5-二溴苯-1,4-二甲醛 在 ammonium acetate 、 溶剂黄146 作用下, 以85 %的产率得到2-(2',3-dibromo-4-formyl-phenyl)imidazo[4,5-f][1,10]-phenanthroline
    参考文献:
    名称:
    Design, synthesis and biological evaluation of liposome entrapped iridium(III) complexes toward SGC-7901 cells
    摘要:
    DOI:
    10.1016/j.jinorgbio.2023.112134
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文献信息

  • DNA binding, photocleavage and topoisomerase inhibitory activity of polypyridyl ruthenium(II) complexes containing the same ancillary ligand and different main ligands
    作者:Xiaojun He、Leli Zeng、Guang Yang、Lingjun Xie、Xiaonan Sun、Lifeng Tan
    DOI:10.1016/j.ica.2013.08.010
    日期:2013.11
    The binding and photocleavage properties of [Ru(phen)(2)L](2+) where phen is 1,10- phenanthroline and L is 2-(4-formylphenyl)imidazo[4,5-f][1,10] phenanthroline (fmp) or 2-(2',3-dibromo-4-formyl-phenyl)imidazo[4,5-f][1,10]-phenanthroline (fmp-2Br)} with regard to DNA were investigated using various biophysical techniques. Results suggest that the two complexes can bind to DNA via an intercalative mode with different affinities and efficiently photocleavage pBR322 DNA in vitro under irradiation. Furthermore, the results of topoisomerase inhibition and DNA strand passage assay reflect that both complexes are efficient dual topoisomerase I and IIa inhibitors. (c) 2013 Elsevier B. V. All rights reserved.
  • Design, synthesis and biological evaluation of liposome entrapped iridium(III) complexes toward SGC-7901 cells
    作者:Yichuan Chen、Yiying Gu、Huiyan Hu、Haimei Liu、Wenlong Li、Chunxia Huang、Jing Chen、Lijuan Liang、Yunjun Liu
    DOI:10.1016/j.jinorgbio.2023.112134
    日期:2023.4
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