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aluminum 5-fluoro-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ide chloride hydroxide | 191284-81-8

中文名称
——
中文别名
——
英文名称
aluminum 5-fluoro-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ide chloride hydroxide
英文别名
——
aluminum 5-fluoro-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ide chloride hydroxide化学式
CAS
191284-81-8
化学式
Al*C4H2FN2O2*Cl*HO
mdl
——
分子量
208.512
InChiKey
MFELUMROZSRKIB-UHFFFAOYSA-K
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):
    -4.72
  • 重原子数:
    12.0
  • 可旋转键数:
    0.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    94.03
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    5-Fluorouracil and 5-fluorouracil-histidine complexes with AlIII, CrIII and FeIII ions and their antitumour activity
    摘要:
    Complexes of the type [M(L-H)(OH)Cl], [Cr(L-H)(H2O)(2)(OH)Cl] and [M'(L-H)(L'-H)(H2O)Cl], where L = 5-fluorouracil; L' = histidine (HISD); M = Al-III or Fe-III and M' = Al-III, Cr-III or Fe-III were synthesized and characterized. The complexes are insoluble in water and common organic solvents. 5-Fluorouracil is coordinated to the metal ion through the O atom of C-(4)=O and the N atom of N-(1) while histidine coordinates through the O atom of -COO- and the N atom of -NH2 groups. The mu(eff) values, electronic spectral bands and ESR spectra suggest a polymeric 6-coordinate spin free octahedral stereochemistry for Cr-III and Fe-III complexes. The in vivo antitumour effect of 5-fluorouracil and its complexes was examined on C3H/He mice against P815 murine mastocytoma. As evident from their T/C values Cr-III and Fe-III complexes display significant and higher antitumour activity compared to 5-fluorouracil while the Al-III complexes show lower activity. The in vitro results of the complexes on the same cells indicate that Cr-III and Fe-III complexes show higher inhibition on H-3-thymidine and H-3-uridine incorporation in DNA and RNA replication, respectively. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0277-5387(96)00551-7
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