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[PbII(2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol)NO3] | 1567836-13-8

中文名称
——
中文别名
——
英文名称
[PbII(2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol)NO3]
英文别名
[PbII(Liodo)NO3]
[Pb<sup>II</sup>(2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol)NO<sub>3</sub>]化学式
CAS
1567836-13-8
化学式
C13H11I2N3O4Pb
mdl
——
分子量
734.257
InChiKey
XYTNHIPLZFAVJE-UHFFFAOYSA-M
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:
    lead(II) nitrate2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol三乙胺 作用下, 以 乙醇 为溶剂, 反应 24.0h, 以86%的产率得到[PbII(2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol)NO3]
    参考文献:
    名称:
    Inhibition of the 26S proteasome as a possible mechanism for toxicity of heavy metal species
    摘要:
    In this paper we report on the synthesis of five metal complexes coordinated to the [NN'O] ligand HL(iodo) (2,4-diiodo-6-((pyridine-2-ylmethylamino)methyl)phenol), namely [Al(III)(L(iodo))2]ClO4 (1), [Cd(II)(L(iodo))Cl]·H2O (2), [Hg(II)(L(iodo))2]·4DMSO (3), [Pb(II)(L(iodo))NO3] (4), and [Sn(IV)(L(iodo))Cl3] (5). Species 1-5 are thoroughly characterized by spectroscopic and spectrometric methods, as well as by elemental analysis. X-ray crystallography results for complex 3 indicate the presence of Hg(II) ion hexacoordinated to two facially oriented [NN'O] ligands, whereas for complex 5 an Sn(IV) ion chelates to one deprotonated ligand and three chlorido coligands. The toxicity of species 1-5 is tested against transformed human prostate epithelial cells CRL2221 and we observe that the five complexes demonstrate high levels of cell growth inhibition in a dose-dependent manner. In order to evaluate the relationship between these species and the proteasome, we test 1-5 against purified 20S, CRL2221 cell extracts, and intact cells, followed by the measurement of the percent chymotrypsin-like activity inhibition levels. Results suggest a good correlation between the toxicity of [Hg(II)(L(iodo))2]·4DMSO (3) and proteasome inhibition.
    DOI:
    10.1016/j.jinorgbio.2013.12.012
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