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6,7-dicyano-5,8-quinolinedione | 102072-70-8

中文名称
——
中文别名
——
英文名称
6,7-dicyano-5,8-quinolinedione
英文别名
5,8-Dioxoquinoline-6,7-dicarbonitrile;5,8-dioxoquinoline-6,7-dicarbonitrile
6,7-dicyano-5,8-quinolinedione化学式
CAS
102072-70-8
化学式
C11H3N3O2
mdl
——
分子量
209.164
InChiKey
MUUXZRNERSDSJG-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:
    16
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    94.6
  • 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:
    6,7-二氯-5,8-喹啉二酮硝酸 作用下, 以 四氢呋喃甲醇乙酸酐 为溶剂, 反应 0.03h, 生成 6,7-dicyano-5,8-quinolinedione
    参考文献:
    名称:
    Streptonigrin. 1. Structure-activity relationships among simple bicyclic analogs. Rate dependence of DNA degradation on quinone reduction potential
    摘要:
    A series of simple aza and diaza bicyclic quinones related to the AB ring system of streptonigrin (1) have been synthesized and tested in vitro for their ability to degrade DNA under conditions similar to those used with the parent drug. The results obtained from a study of 22 quinones indicate that there is a quantitative linear relationship between their reduction potentials and the rate at which they degrade DNA under identical conditions in vitro. Almost all of the synthetic substances were superior to 1 in their DNA-degrading ability.
    DOI:
    10.1021/jm00158a002
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文献信息

  • Streptonigrin. 1. Structure-activity relationships among simple bicyclic analogs. Rate dependence of DNA degradation on quinone reduction potential
    作者:Iftikhar A. Shaikh、Francis Johnson、Arthur P. Grollman
    DOI:10.1021/jm00158a002
    日期:1986.8
    A series of simple aza and diaza bicyclic quinones related to the AB ring system of streptonigrin (1) have been synthesized and tested in vitro for their ability to degrade DNA under conditions similar to those used with the parent drug. The results obtained from a study of 22 quinones indicate that there is a quantitative linear relationship between their reduction potentials and the rate at which they degrade DNA under identical conditions in vitro. Almost all of the synthetic substances were superior to 1 in their DNA-degrading ability.
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