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(6-((methyl(2-(methylamino)ethyl)amino)methyl)pyridin-2-yl)methanol | 1342295-66-2

中文名称
——
中文别名
——
英文名称
(6-((methyl(2-(methylamino)ethyl)amino)methyl)pyridin-2-yl)methanol
英文别名
——
(6-((methyl(2-(methylamino)ethyl)amino)methyl)pyridin-2-yl)methanol化学式
CAS
1342295-66-2
化学式
C11H19N3O
mdl
——
分子量
209.291
InChiKey
YZIQZDYMPANKPC-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):
    0.23
  • 重原子数:
    15.0
  • 可旋转键数:
    6.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    48.39
  • 氢给体数:
    2.0
  • 氢受体数:
    4.0

上下游信息

  • 下游产品
    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:
    描述:
    9-氯甲基蒽(6-((methyl(2-(methylamino)ethyl)amino)methyl)pyridin-2-yl)methanolpotassium carbonate 作用下, 以 乙腈 为溶剂, 反应 48.0h, 以75%的产率得到(6-(((2-((anthracen-9-ylmethyl)(methyl)amino)ethyl)(methyl)amino)methyl)pyridin-2-yl)-methanol
    参考文献:
    名称:
    Physiologically Relevant Concentrations of NaCl and KCl Increase DNA Photocleavage by an N-Substituted 9-Aminomethylanthracene Dye
    摘要:
    This paper describes the synthesis of a new 9-aminomethylanthracene dye N-substituted with a pyridinylpoly-amine side chain (4). The effects of NaCl and KCl on anthracene/DNA interactions were then studied, with the goal of simulating the conditions of high ionic strength that a DNA photosensitizer might encounter in the cell nucleus (similar to 450 mM of NaCl and 260 mM of KCl). As exemplified by methylene blue (5), the expected effect of increasing ionic strength is to decrease DNA binding and photocleavage yields. In contrast, the addition of 150 mM of NaCl in combination with 260 mM of KCl to photodeavage reactions containing micromolar concentrations of 4 triggers the conversion of supercoiled, nicked, and linear forms of pUC19 plasmid into a highly degraded band of DNA fragments (350 nm hv, pH 7.0). Circular dichroism spectra point to a correlation between salt-induced unwinding of the DNA helix and the increase in DNA photocleavage yields. The results of circular dichroism, UV-vis absorption, fluorescence emission, thermal denaturation, and photodeavage inhibition experiments suggest that the combination of salts causes a change in the DNA binding mode of 4 from intercalation to an external interaction. This in turn leads to an increase in the anthracene-sensitized production of DNA-damaging reactive oxygen species.
    DOI:
    10.1021/bi200972c
  • 作为产物:
    描述:
    N,N'-二甲基乙二胺6-溴甲基-2-吡啶甲醇potassium carbonate 作用下, 以 乙腈 为溶剂, 反应 4.5h, 以90%的产率得到(6-((methyl(2-(methylamino)ethyl)amino)methyl)pyridin-2-yl)methanol
    参考文献:
    名称:
    Physiologically Relevant Concentrations of NaCl and KCl Increase DNA Photocleavage by an N-Substituted 9-Aminomethylanthracene Dye
    摘要:
    This paper describes the synthesis of a new 9-aminomethylanthracene dye N-substituted with a pyridinylpoly-amine side chain (4). The effects of NaCl and KCl on anthracene/DNA interactions were then studied, with the goal of simulating the conditions of high ionic strength that a DNA photosensitizer might encounter in the cell nucleus (similar to 450 mM of NaCl and 260 mM of KCl). As exemplified by methylene blue (5), the expected effect of increasing ionic strength is to decrease DNA binding and photocleavage yields. In contrast, the addition of 150 mM of NaCl in combination with 260 mM of KCl to photodeavage reactions containing micromolar concentrations of 4 triggers the conversion of supercoiled, nicked, and linear forms of pUC19 plasmid into a highly degraded band of DNA fragments (350 nm hv, pH 7.0). Circular dichroism spectra point to a correlation between salt-induced unwinding of the DNA helix and the increase in DNA photocleavage yields. The results of circular dichroism, UV-vis absorption, fluorescence emission, thermal denaturation, and photodeavage inhibition experiments suggest that the combination of salts causes a change in the DNA binding mode of 4 from intercalation to an external interaction. This in turn leads to an increase in the anthracene-sensitized production of DNA-damaging reactive oxygen species.
    DOI:
    10.1021/bi200972c
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