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N-(2-hydroxyethyl)-2-(4-nitro-1H-imidazol-1-yl)acetamide | 1153126-46-5

中文名称
——
中文别名
——
英文名称
N-(2-hydroxyethyl)-2-(4-nitro-1H-imidazol-1-yl)acetamide
英文别名
N-(2-hydroxyethyl)-2-(4-nitroimidazol-1-yl)acetamide
N-(2-hydroxyethyl)-2-(4-nitro-1H-imidazol-1-yl)acetamide化学式
CAS
1153126-46-5
化学式
C7H10N4O4
mdl
——
分子量
214.181
InChiKey
JCLHJCMUTOCOCC-UHFFFAOYSA-N
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):
    -1.1
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    113
  • 氢给体数:
    2
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and fluorescent characteristics of imidazole–indocyanine green conjugates
    摘要:
    We have successfully synthesized imidazole-dye conjugates by linking imidazole and nitroimidazoleacetic acids to an indocyanine green (ICG) carboxylic acid derivative using an ethanolamine linker These dye-conjugates show absorbance peaks at 754-756 nm and fluorescence peaks at 780 rim The dye-conjugates show a blue shift of 25 nm and 30 nm in the absorption and fluorescence spectra respectively when compared to that of standard cardiogreen There is no change in absorption and fluorescence spectral profiles between the ICG derivative and imidazole conjugates The extinction coefficients of new ICG derivative and imidazole conjugates are 1 8 times higher than that of standard ICG The relative quantum yields of the new compounds are 4 5-5 5 times higher than that of the Sigma-Aldrich s ICG The dyes are tested for hypoxia in-vitro with 4T1 luc cell lines and it is found that the cells treated with 2-nitroimidazole ICG show a contrast of fluorescence signal of 2 5-30 for the cells under hypoxic to that of cells under normoxic However pure ICG shows no significant difference between hypoxic and normoxic cells (C) 2010 Elsevier Ltd All rights reserved
    DOI:
    10.1016/j.dyepig.2010.08.008
  • 作为产物:
    描述:
    C.I.酸性橙108(4-硝基咪唑-1-基)乙酸甲酯甲醇 为溶剂, 反应 24.0h, 以0.587 g的产率得到N-(2-hydroxyethyl)-2-(4-nitro-1H-imidazol-1-yl)acetamide
    参考文献:
    名称:
    Synthesis and fluorescent characteristics of imidazole–indocyanine green conjugates
    摘要:
    We have successfully synthesized imidazole-dye conjugates by linking imidazole and nitroimidazoleacetic acids to an indocyanine green (ICG) carboxylic acid derivative using an ethanolamine linker These dye-conjugates show absorbance peaks at 754-756 nm and fluorescence peaks at 780 rim The dye-conjugates show a blue shift of 25 nm and 30 nm in the absorption and fluorescence spectra respectively when compared to that of standard cardiogreen There is no change in absorption and fluorescence spectral profiles between the ICG derivative and imidazole conjugates The extinction coefficients of new ICG derivative and imidazole conjugates are 1 8 times higher than that of standard ICG The relative quantum yields of the new compounds are 4 5-5 5 times higher than that of the Sigma-Aldrich s ICG The dyes are tested for hypoxia in-vitro with 4T1 luc cell lines and it is found that the cells treated with 2-nitroimidazole ICG show a contrast of fluorescence signal of 2 5-30 for the cells under hypoxic to that of cells under normoxic However pure ICG shows no significant difference between hypoxic and normoxic cells (C) 2010 Elsevier Ltd All rights reserved
    DOI:
    10.1016/j.dyepig.2010.08.008
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