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[(tris(2-aminoethyl)amine) zinc (hydrogentriothiocyanurate)]*water | 942477-47-6

中文名称
——
中文别名
——
英文名称
[(tris(2-aminoethyl)amine) zinc (hydrogentriothiocyanurate)]*water
英文别名
——
[(tris(2-aminoethyl)amine) zinc (hydrogentriothiocyanurate)]*water化学式
CAS
942477-47-6
化学式
C9H19N7S3Zn*H2O
mdl
——
分子量
404.9
InChiKey
YIJWKQAAWFBWNE-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:
    sodium 2,4,6-trimercapto-1,3,5-triazinate nonahydrate 、 三(2-氨基乙基)胺zinc(II) acetate dihydrate 在 NaOH 作用下, 以 乙醇 为溶剂, 以67%的产率得到[(tris(2-aminoethyl)amine) zinc (hydrogentriothiocyanurate)]*water
    参考文献:
    名称:
    Synthesis, characterization and screening of biological activity of Zn(II), Fe(II) and Mn(II) complexes with trithiocyanuric acid
    摘要:
    New Zn(II), Fe(II) and Mn(II) complexes with a combination of nitrogen-donor ligands and trithiocyanuric acid (ttcH(3)) were prepared and characterized by elemental analysis, IR and UV-Vis spectroscopies. The antitumor activity of the prepared complexes, together with already known Ni(II) species, were assayed in vitro against G-361 (human malignant melanoma), HOS (human osteogenic sarcoma), K-562 (human chronic myelogenous leukaemia) and MCF-7 (human breast adenocarcinoma) tumor cell lines. The IC50 values of the Fe(II) and Mn(II) compounds turned out to be lower than those of cisplatin and oxaliplatin. The antimicrobial activities were evaluated by MIC against bacteria (Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus and Enterococcus faecalis). The molecular structure of [Zn(taa)(ttcH)] center dot H2O (taa = tris(2-aminoethyl)amine) was determined by X-ray diffraction. The central atom is pentacoordinated by four N atoms of taa and one N atom of the ttcH dianion. (C) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2006.11.022
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