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2-(6-(2-methoxybenzylamino)hexylamino)naphthalene-1,4-dione | 1350890-30-0

中文名称
——
中文别名
——
英文名称
2-(6-(2-methoxybenzylamino)hexylamino)naphthalene-1,4-dione
英文别名
2-[6-[(2-Methoxyphenyl)methylamino]hexylamino]naphthalene-1,4-dione
2-(6-(2-methoxybenzylamino)hexylamino)naphthalene-1,4-dione化学式
CAS
1350890-30-0
化学式
C24H28N2O3
mdl
——
分子量
392.498
InChiKey
YOWLFNDAAHIOHS-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):
    4.3
  • 重原子数:
    29
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    67.4
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    2-(6-(2-methoxybenzylamino)hexylamino)naphthalene-1,4-dione盐酸 作用下, 以 为溶剂, 以16%的产率得到2-(6-(2-methoxybenzylamino)hexylamino)naphthalene-1,4-dione hydrochloride
    参考文献:
    名称:
    Synthesis of Monomeric Derivatives To Probe Memoquin’s Bivalent Interactions
    摘要:
    Eight monomeric congeners, related to the multitarget lead candidate memoquin, were prepared and evaluated at multiple targets to determine their profile against Alzheimer's disease. 2-4 bind to AChE with similar low nanomolar affinities and function as effective inhibitors of amyloid aggregation. The most potent monovalent ligand 2 also inhibits BACE-1 in vitro and APP metabolism in primary chicken telencephalic neurons.
    DOI:
    10.1021/jm200691d
  • 作为产物:
    描述:
    [(2-methoxyphenyl)methyl][6-(methylamino)hexyl]amine1,4-萘醌甲醇 为溶剂, 反应 4.0h, 以0.14 g的产率得到2-(6-(2-methoxybenzylamino)hexylamino)naphthalene-1,4-dione
    参考文献:
    名称:
    Synthesis of Monomeric Derivatives To Probe Memoquin’s Bivalent Interactions
    摘要:
    Eight monomeric congeners, related to the multitarget lead candidate memoquin, were prepared and evaluated at multiple targets to determine their profile against Alzheimer's disease. 2-4 bind to AChE with similar low nanomolar affinities and function as effective inhibitors of amyloid aggregation. The most potent monovalent ligand 2 also inhibits BACE-1 in vitro and APP metabolism in primary chicken telencephalic neurons.
    DOI:
    10.1021/jm200691d
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文献信息

  • Synthesis of Monomeric Derivatives To Probe Memoquin’s Bivalent Interactions
    作者:Maria Laura Bolognesi、GianPaolo Chiriano、Manuela Bartolini、Francesca Mancini、Giovanni Bottegoni、Valentina Maestri、Stefan Czvitkovich、Manfred Windisch、Andrea Cavalli、Anna Minarini、Michela Rosini、Vincenzo Tumiatti、Vincenza Andrisano、Carlo Melchiorre
    DOI:10.1021/jm200691d
    日期:2011.12.22
    Eight monomeric congeners, related to the multitarget lead candidate memoquin, were prepared and evaluated at multiple targets to determine their profile against Alzheimer's disease. 2-4 bind to AChE with similar low nanomolar affinities and function as effective inhibitors of amyloid aggregation. The most potent monovalent ligand 2 also inhibits BACE-1 in vitro and APP metabolism in primary chicken telencephalic neurons.
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