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9-[(2-Hydroxyethyl)amino]-6-[2-(4-methoxyphenyl)ethyl]pyrido[2',1':2,3]imidazo[4,5-c]isoquinolin-5(6H)-one | 1228832-02-7

中文名称
——
中文别名
——
英文名称
9-[(2-Hydroxyethyl)amino]-6-[2-(4-methoxyphenyl)ethyl]pyrido[2',1':2,3]imidazo[4,5-c]isoquinolin-5(6H)-one
英文别名
13-(2-Hydroxyethylamino)-9-[2-(4-methoxyphenyl)ethyl]-9,11,17-triazatetracyclo[8.7.0.02,7.011,16]heptadeca-1(10),2,4,6,12,14,16-heptaen-8-one
9-[(2-Hydroxyethyl)amino]-6-[2-(4-methoxyphenyl)ethyl]pyrido[2',1':2,3]imidazo[4,5-c]isoquinolin-5(6H)-one化学式
CAS
1228832-02-7
化学式
C25H24N4O3
mdl
——
分子量
428.491
InChiKey
CYHUXURZLLLNLH-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):
    4.1
  • 重原子数:
    32
  • 可旋转键数:
    7
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    79.1
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    9-bromo-6-(4-methoxyphenethyl)pyrido[2',1':2,3]imidazo[4,5-c]isoquinolin-5(6H)-one 、 C.I.酸性橙108copper(l) iodidepotassium carbonateL-脯氨酸 作用下, 以 二甲基亚砜 为溶剂, 反应 0.17h, 以80%的产率得到9-[(2-Hydroxyethyl)amino]-6-[2-(4-methoxyphenyl)ethyl]pyrido[2',1':2,3]imidazo[4,5-c]isoquinolin-5(6H)-one
    参考文献:
    名称:
    Synthesis and biological evaluation of 6H-pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5(6H)-ones as antimitotic agents and inhibitors of tubulin polymerization
    摘要:
    A series of 6H-pyrido[20,10: 2,3] imidazo[4,5-c] isoquinolin-5(6H)-ones have been synthesized and evaluated for their antiproliferative activities. Among them, compounds 2j and 4d displayed potent cytotoxic activities in vitro against HeLa cell line with IC50 values of 0.07 and 0.06 mu M, respectively. In general, the antiproliferative activities are correlated with the inhibitory effect on tubulin polymerization and binding property of the colchicine binding site. In addition, flow cytometry and immunofluorescence analysis revealed selected compounds caused G2/M phase arrest of the cell cycle and disruption of the mitotic spindle assembly, which had correlation with proliferation inhibitory activity. (C) 2014 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmc.2013.12.004
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文献信息

  • Synthesis and biological evaluation of 6H-pyrido[2′,1′:2,3]imidazo[4,5-c]isoquinolin-5(6H)-ones as antimitotic agents and inhibitors of tubulin polymerization
    作者:Tao Meng、Wei Wang、Zhixiang Zhang、Lanping Ma、Yongliang Zhang、Zehong Miao、Jingkang Shen
    DOI:10.1016/j.bmc.2013.12.004
    日期:2014.1
    A series of 6H-pyrido[20,10: 2,3] imidazo[4,5-c] isoquinolin-5(6H)-ones have been synthesized and evaluated for their antiproliferative activities. Among them, compounds 2j and 4d displayed potent cytotoxic activities in vitro against HeLa cell line with IC50 values of 0.07 and 0.06 mu M, respectively. In general, the antiproliferative activities are correlated with the inhibitory effect on tubulin polymerization and binding property of the colchicine binding site. In addition, flow cytometry and immunofluorescence analysis revealed selected compounds caused G2/M phase arrest of the cell cycle and disruption of the mitotic spindle assembly, which had correlation with proliferation inhibitory activity. (C) 2014 Published by Elsevier Ltd.
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