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2,8-dimethoxy-11H-indolo[3,2-c]quinoline | 710944-43-7

中文名称
——
中文别名
——
英文名称
2,8-dimethoxy-11H-indolo[3,2-c]quinoline
英文别名
——
2,8-dimethoxy-11H-indolo[3,2-c]quinoline化学式
CAS
710944-43-7
化学式
C17H14N2O2
mdl
——
分子量
278.31
InChiKey
VROKBFHTRLGPDN-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):
    3.89
  • 重原子数:
    21.0
  • 可旋转键数:
    2.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    47.14
  • 氢给体数:
    1.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    2,8-dimethoxy-11H-indolo[3,2-c]quinoline氢溴酸potassium carbonate 作用下, 以 甲醇氯仿溶剂黄146 为溶剂, 反应 48.0h, 生成 2-[[2-[2-(dimethylamino)ethoxy]-11H-indolo[3,2-c]quinolin-8-yl]oxy]-N,N-dimethylethanamine
    参考文献:
    名称:
    Design of antineoplastic agents based on the '2-phenylnaphthalene-type' structural pattern—synthesis and biological activity studies of 11H-indolo[3.2-c]quinoline derivatives
    摘要:
    Designed as a new group of planar molecule containing the proposed 2-phenylnaphthalene-type structure, a number of 11H-indolo[3.2-c]quinoline derivatives were synthesized and evaluated biologically. Several compounds were found to possess cytotoxic activity against the growth of human promyclocytic leukemia cells (HL-60), against the small cell lung cancer (SCLC), and showed good response in the National Cancer Institute preclinical antitumor drug discovery 60-cell line panel. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
    DOI:
    10.1016/s0223-5234(02)01420-4
  • 作为产物:
    描述:
    6-甲氧基-2,3-二氢喹啉-4-酮(4-甲氧基苯基)肼盐酸 作用下, 以 正丁醇 为溶剂, 反应 20.0h, 以47%的产率得到2,8-dimethoxy-11H-indolo[3,2-c]quinoline
    参考文献:
    名称:
    Design of antineoplastic agents based on the '2-phenylnaphthalene-type' structural pattern—synthesis and biological activity studies of 11H-indolo[3.2-c]quinoline derivatives
    摘要:
    Designed as a new group of planar molecule containing the proposed 2-phenylnaphthalene-type structure, a number of 11H-indolo[3.2-c]quinoline derivatives were synthesized and evaluated biologically. Several compounds were found to possess cytotoxic activity against the growth of human promyclocytic leukemia cells (HL-60), against the small cell lung cancer (SCLC), and showed good response in the National Cancer Institute preclinical antitumor drug discovery 60-cell line panel. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
    DOI:
    10.1016/s0223-5234(02)01420-4
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