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[Cu(Fc-CH2NHCCH2C6H5OH)(1,10-phenanthroline)](ClO4) | 1429908-48-4

中文名称
——
中文别名
——
英文名称
[Cu(Fc-CH2NHCCH2C6H5OH)(1,10-phenanthroline)](ClO4)
英文别名
——
[Cu(Fc-CH2NHCCH2C6H5OH)(1,10-phenanthroline)](ClO4)化学式
CAS
1429908-48-4
化学式
C32H28CuFeN3O3*ClO4
mdl
——
分子量
721.436
InChiKey
PXRBLSGPOGABSZ-NLQDPJAYSA-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:
    1,10-菲罗啉 、 Ferrocenyl-tyrosine 、 sodium perchlorate 、 copper(II) acetate monohydrate甲醇 为溶剂, 反应 1.5h, 以74%的产率得到[Cu(Fc-CH2NHCCH2C6H5OH)(1,10-phenanthroline)](ClO4)
    参考文献:
    名称:
    Photocytotoxic ferrocene-appended (l-tyrosine)copper(II) complexes of phenanthroline bases
    摘要:
    Copper(II) complexes of ferrocene(Fc)-conjugated reduced Schiff base of L-tyrosine (Fc-TyrH), viz., [Cu(Fc-Tyr)(L)](ClO4), where L is 1,10-phenanthroline (phen, 1), dipyrido[3,2-d:2',3'-f]quinoxaline (dpq, 2), dipyrido[3,2-a:2',3'-c]phenazine (dppz, 3) and 2-(naphthalen-1-yl)-1H-imidazo[4,5-f][1,10]phenanthroline (nip, 4), were prepared and tested for their photocytotoxicity in cancer cells. [Cu(Fc-Phe)(phen)](-ClO4) (5) of L-phenylalanine and [Cu(Ph-Tyr)(L)(ClO4)] of the reduced Schiff base Ph-TyrH derived from benzaldehyde and L-tyrosine having phen (6) and dppz (7), and [Cu(Ph-Phe)(phen)(ClO4)] (8) using L-phenylalanine were prepared and used as controls. Complexes 5 and 6 were structurally characterized by X-ray crystallography. A copper(II)-based d-d band near 600 nm and a ferrocenyl band at similar to 450 nm were observed in DMF-Tris-HCI buffer (1:4 v/v) in respective complexes. The complexes are photocleavers of pUC19 DNA in visible light forming (OH)-O-center dot radicals. They are cytotoxic in HeLa (human cervical cancer) and MCF-7 (human breast cancer) cells showing an enhancement of cytotoxicity in visible light. Fluorescence imaging shows nuclear localization of the complexes. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2012.06.018
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