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[CuZnBr2(N,N'-bis(3-ethoxysalicylidene)-1,3-propanediamine-2H)] | 1326634-66-5

中文名称
——
中文别名
——
英文名称
[CuZnBr2(N,N'-bis(3-ethoxysalicylidene)-1,3-propanediamine-2H)]
英文别名
——
[CuZnBr2(N,N'-bis(3-ethoxysalicylidene)-1,3-propanediamine-2H)]化学式
CAS
1326634-66-5
化学式
C21H24Br2CuN2O4Zn
mdl
——
分子量
657.177
InChiKey
IMXOXVGSGUJYHP-GHBXDJGSSA-J
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:
    copper(II) perchlorate hexahydrate 、 N,N'-bis(3-ethoxysalicylidenimino)-1,3-diaminopropane 、 zinc dibromide 以 甲醇 为溶剂, 以78%的产率得到[CuZnBr2(N,N'-bis(3-ethoxysalicylidene)-1,3-propanediamine-2H)]
    参考文献:
    名称:
    Preparation and structural characterization of hetero-dinuclear Schiff base copper(II)–zinc(II) complexes and their inhibition studies on Helicobacter pylori urease
    摘要:
    A series of hetero-dinuclear Cu-II-Zn-II complexes, [CuZnCl2L1] (1), [CuZnCl2L2] (2), [CuZnBr2L3] (3), [CuZnBr2L4(DMF)] (4), [CuZnCl2L4] (5), [CuZnCl2L5] (6), [CuZnCl2L3] (7) and [CuZnBr2L1] (8), where L-3, L-4 and L-5 are the deprotonated forms of N,N'-bis(3-ethoxysalicylidene)-1,3-propanediamine (H2L1), N,N'-bis(2-hydroxynaphthylmethylidene)-1,3-propanediamine (H2L2), N,N'-bis(3-methoxysalicylidene)-1,3-propanediamine (H2L3), N,N'-bis(salicylidene)-1,3-propanediamine (H2L4) and N,N'-bis(salicylidene)1,4-butanediamine (H2L5), respectively, have been synthesized and characterized by physico-chemical methods and single-crystal X-ray diffraction. The complexes were tested for their urease inhibitory activity. Complexes 1 and 8 show effective urease inhibitory activity with IC50 values of 2.2 and 10.7 mu M. The molecular docking study of the complexes with the Helicobacter pylori urease was performed. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.poly.2011.05.048
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