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11H-Indolo[3,2-c]quinolin-8-ol | 766505-43-5

中文名称
——
中文别名
——
英文名称
11H-Indolo[3,2-c]quinolin-8-ol
英文别名
——
11H-Indolo[3,2-c]quinolin-8-ol化学式
CAS
766505-43-5
化学式
C15H10N2O
mdl
——
分子量
234.257
InChiKey
SZRYJIWTHHWMJF-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):
    3.3
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    48.9
  • 氢给体数:
    2
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    二甲氨基氯乙烷盐酸11H-Indolo[3,2-c]quinolin-8-olpotassium carbonate 作用下, 以 氯仿 为溶剂, 反应 28.0h, 以75%的产率得到[2-(11H-Indolo[3,2-c]quinolin-8-yloxy)-ethyl]-dimethyl-amine
    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:
    2,3-二氢-1H-喹啉-4-酮盐酸氢溴酸 作用下, 以 溶剂黄146正丁醇 为溶剂, 反应 30.0h, 生成 11H-Indolo[3,2-c]quinolin-8-ol
    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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文献信息

  • 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
    作者:L He
    DOI:10.1016/s0223-5234(02)01420-4
    日期:2003.1
    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.
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