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5-Amino-2-[3-(3-aminopropylamino)propyl]benzo[de]isoquinoline-1,3-dione

中文名称
——
中文别名
——
英文名称
5-Amino-2-[3-(3-aminopropylamino)propyl]benzo[de]isoquinoline-1,3-dione
英文别名
——
5-Amino-2-[3-(3-aminopropylamino)propyl]benzo[de]isoquinoline-1,3-dione化学式
CAS
——
化学式
C18H22N4O2
mdl
——
分子量
326.398
InChiKey
POYQQIIKSMDNMW-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):
    0.8
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    101
  • 氢给体数:
    3
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    6,7-dihydroindeno[6,7,1-def]isochromene-1,3-dione5-Amino-2-[3-(3-aminopropylamino)propyl]benzo[de]isoquinoline-1,3-dione乙醇 为溶剂, 以37%的产率得到6-{3-[3-(5-Amino-1,3-dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-propylamino]-propyl}-1,2-dihydro-6-aza-cyclopenta[cd]phenalene-5,7-dione
    参考文献:
    名称:
    Bis-naphthalimides. 2. Synthesis and biological activity of 5,6-acenaphthalimidoalkyl-1,8-naphthalimidoalkyl amines
    摘要:
    A series of non-symmetric bis-naphthalimides bearing a conveniently substituted 1,8-naphthalimide and a 5,6-acenaphthalimide chromophore was synthesized and in vitro activities were determined. Although previous studies suggested that the presence of the acenaphthalimide system in the structure enhances aqueous solubility, we found that these compounds were no more soluble or cytotoxic than the homologous symmetric series.
    DOI:
    10.1016/0223-5234(96)88230-4
  • 作为产物:
    描述:
    3,3'-二氨基二丙基胺3-amino-naphthalene-1,8-dicarboxylic acid-anhydrideN,N-二甲基甲酰胺 为溶剂, 反应 15.0h, 以13%的产率得到5-Amino-2-[3-(3-aminopropylamino)propyl]benzo[de]isoquinoline-1,3-dione
    参考文献:
    名称:
    Bis-naphthalimides. 2. Synthesis and biological activity of 5,6-acenaphthalimidoalkyl-1,8-naphthalimidoalkyl amines
    摘要:
    A series of non-symmetric bis-naphthalimides bearing a conveniently substituted 1,8-naphthalimide and a 5,6-acenaphthalimide chromophore was synthesized and in vitro activities were determined. Although previous studies suggested that the presence of the acenaphthalimide system in the structure enhances aqueous solubility, we found that these compounds were no more soluble or cytotoxic than the homologous symmetric series.
    DOI:
    10.1016/0223-5234(96)88230-4
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文献信息

  • US5554622A
    申请人:——
    公开号:US5554622A
    公开(公告)日:1996-09-10
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