摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1,4-dihydro-5,11-dimethyl-2-ethyl-4-oxo-6H-pyrido<3,2-b>carbazole | 144099-01-4

中文名称
——
中文别名
——
英文名称
1,4-dihydro-5,11-dimethyl-2-ethyl-4-oxo-6H-pyrido<3,2-b>carbazole
英文别名
2-Ethyl-5,11-dimethyl-1,6-dihydropyrido[3,2-b]carbazol-4-one
1,4-dihydro-5,11-dimethyl-2-ethyl-4-oxo-6H-pyrido<3,2-b>carbazole化学式
CAS
144099-01-4;153334-69-1
化学式
C19H18N2O
mdl
——
分子量
290.365
InChiKey
CFHOPBFSTWVUBE-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):
    4.6
  • 重原子数:
    22
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.21
  • 拓扑面积:
    44.9
  • 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:
    乙酸酐1,4-dihydro-5,11-dimethyl-2-ethyl-4-oxo-6H-pyrido<3,2-b>carbazole溶剂黄146 作用下, 反应 1.0h, 以49%的产率得到4-acetoxy-2,3,5,11-tetramethyl-6H-pyrido<3,2-b>carbazole
    参考文献:
    名称:
    In vitro cytotoxicity of carbazole derivatives IV. 5,11-Dimethyl-6H-pyrido[3,2-b]carbazoles substituted on the pyridine ring
    摘要:
    A series of 5,11-dimethyl-6H-pyrido[3,2-b]carbazoles, structurally related to the antitumor drug ellipticine, were synthesized from 3-amino-1,4-dimethyl-9H-carbazole. Among 17 derivatives, bearing various substituents on the pyridine ring, and preliminarily evaluated for cytotoxicity on L1210-cultured cells, 13 (76%) were found to be active. One of them, 5,11-dimethyl-4-ethoxy-6H-pyrido[3,2-b]carbazole, although non-substituted on C-9, displayed an activity similar to that of 9-hydroxy-N-2-methylellipticinium acetate. Structure-activity relationships have been described in detail.
    DOI:
    10.1016/0223-5234(93)90032-a
  • 作为产物:
    参考文献:
    名称:
    In vitro cytotoxicity of carbazole derivatives IV. 5,11-Dimethyl-6H-pyrido[3,2-b]carbazoles substituted on the pyridine ring
    摘要:
    A series of 5,11-dimethyl-6H-pyrido[3,2-b]carbazoles, structurally related to the antitumor drug ellipticine, were synthesized from 3-amino-1,4-dimethyl-9H-carbazole. Among 17 derivatives, bearing various substituents on the pyridine ring, and preliminarily evaluated for cytotoxicity on L1210-cultured cells, 13 (76%) were found to be active. One of them, 5,11-dimethyl-4-ethoxy-6H-pyrido[3,2-b]carbazole, although non-substituted on C-9, displayed an activity similar to that of 9-hydroxy-N-2-methylellipticinium acetate. Structure-activity relationships have been described in detail.
    DOI:
    10.1016/0223-5234(93)90032-a
点击查看最新优质反应信息

文献信息

  • Moinet-Hedin V., Tabka T., Gauduchon P., Le Talaer J. Y., Letois B., Lanc+, Eur. J. Med. Chem, 28 (1993) N 9, S 721-726
    作者:Moinet-Hedin V., Tabka T., Gauduchon P., Le Talaer J. Y., Letois B., Lanc+
    DOI:——
    日期:——
查看更多