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

6-Methylpyrido[2,3-b]phenanthridin-5-one | 1234561-43-3

中文名称
——
中文别名
——
英文名称
6-Methylpyrido[2,3-b]phenanthridin-5-one
英文别名
——
6-Methylpyrido[2,3-b]phenanthridin-5-one化学式
CAS
1234561-43-3
化学式
C17H12N2O
mdl
——
分子量
260.295
InChiKey
ZLWQPHFHCBATFC-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):
    2.9
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    33.2
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    N-methyl-N-(6-quinolinyl)-2-iodobenzamide 在 三丁基膦 、 palladium diacetate 、 silver carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.5h, 以70%的产率得到
    参考文献:
    名称:
    Design and preparation of aza-analogues of benzo[c]phenanthridine framework with cytotoxic and antiplasmodial activities
    摘要:
    Benzo[c]phenanthridine alkaloids represent interesting lead for the discovery of new potential antiplasmodial and/or anticancer drugs. In this field, a novel library of aza-analogs of benzo[c]phenanthroline framework derivatives was designed and prepared. Although these compounds did not have specific antiplasmodial activities, some of them displayed specific in vitro activity against two cancer lines especially compound 24 with an IC(50) against the MCF7 line of 0.6 mu M. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.03.006
点击查看最新优质反应信息

文献信息

  • Design and preparation of aza-analogues of benzo[c]phenanthridine framework with cytotoxic and antiplasmodial activities
    作者:Ange-Désiré Yapi、Nicolas Desbois、Jean-Michel Chezal、Olivier Chavignon、Jean-Claude Teulade、Alexis Valentin、Yves Blache
    DOI:10.1016/j.ejmech.2010.03.006
    日期:2010.7
    Benzo[c]phenanthridine alkaloids represent interesting lead for the discovery of new potential antiplasmodial and/or anticancer drugs. In this field, a novel library of aza-analogs of benzo[c]phenanthroline framework derivatives was designed and prepared. Although these compounds did not have specific antiplasmodial activities, some of them displayed specific in vitro activity against two cancer lines especially compound 24 with an IC(50) against the MCF7 line of 0.6 mu M. (C) 2010 Elsevier Masson SAS. All rights reserved.
查看更多