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3,10,11-Trimethoxy-2,7-diazatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,7-dicarbaldehyde | 1025448-63-8

中文名称
——
中文别名
——
英文名称
3,10,11-Trimethoxy-2,7-diazatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,7-dicarbaldehyde
英文别名
——
3,10,11-Trimethoxy-2,7-diazatricyclo[6.3.1.04,12]dodeca-1(12),8,10-triene-2,7-dicarbaldehyde化学式
CAS
1025448-63-8
化学式
C15H18N2O5
mdl
——
分子量
306.318
InChiKey
NZSGWLXZRUFFSJ-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):
    0.6
  • 重原子数:
    22
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    68.3
  • 氢给体数:
    0
  • 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

  • 作为产物:
    描述:
    甲酸5-氨基-1,2,3,4-四氢-6,7-二甲氧基-4-(二甲氧基甲基)喹啉乙酸酐 作用下, 反应 60.0h, 以36%的产率得到1,5-diformyl-1,3,4,5-tetrahydro-7,8-dimethoxypyrrolo<4,3,2-de>quinoline
    参考文献:
    名称:
    Synthesis and biological evaluation of pyrroloiminoquinone derivatives
    摘要:
    Synthesis of 10 pyrroloiminoquinone derivatives is presented. The strategy is based around the elaboration of a common intermediate by reaction with primary amines. All the compounds obtained have been subjected to antiproliferative activity with three different cell lines (NCI-H460, HeLa, and HL-60). The capacity of 4 selected compounds to affect the enzymatic activity of the nuclear enzyme DNA topoisomerase II and to form the typical DNA fragmentation which occurs in the apoptotic process is discussed here. (C) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2007.11.063
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文献信息

  • Synthesis and biological evaluation of pyrroloiminoquinone derivatives
    作者:Daniele Passarella、Francesca Belinghieri、Michele Scarpellini、Graziella Pratesi、Franco Zunino、Ornella Maria Gia、Lisa Dalla Via、Giuseppe Santoro、Bruno Danieli
    DOI:10.1016/j.bmc.2007.11.063
    日期:2008.3
    Synthesis of 10 pyrroloiminoquinone derivatives is presented. The strategy is based around the elaboration of a common intermediate by reaction with primary amines. All the compounds obtained have been subjected to antiproliferative activity with three different cell lines (NCI-H460, HeLa, and HL-60). The capacity of 4 selected compounds to affect the enzymatic activity of the nuclear enzyme DNA topoisomerase II and to form the typical DNA fragmentation which occurs in the apoptotic process is discussed here. (C) 2007 Elsevier Ltd. All rights reserved.
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