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3-cyclopentyl-3H-benzo[b]imidazo[4,5-g][1,8]naphthyridin-10(5H)-one

中文名称
——
中文别名
——
英文名称
3-cyclopentyl-3H-benzo[b]imidazo[4,5-g][1,8]naphthyridin-10(5H)-one
英文别名
15-Cyclopentyl-2,13,15,17-tetrazatetracyclo[8.7.0.03,8.012,16]heptadeca-1(17),3,5,7,10,12(16),13-heptaen-9-one;15-cyclopentyl-2,13,15,17-tetrazatetracyclo[8.7.0.03,8.012,16]heptadeca-1(17),3,5,7,10,12(16),13-heptaen-9-one
3-cyclopentyl-3H-benzo[b]imidazo[4,5-g][1,8]naphthyridin-10(5H)-one化学式
CAS
——
化学式
C18H16N4O
mdl
——
分子量
304.351
InChiKey
YKJJTJCSRGQRIT-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:
    23
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    59.8
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 下游产品
    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:
    3-cyclopentyl-3H-benzo[b]imidazo[4,5-g][1,8]naphthyridin-10(5H)-oneN,N-二乙基氯乙胺potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 14.0h, 以73%的产率得到3-cyclopentyl-5-(2-diethylaminoethyl)-3H-benzo[b]imidazo[4,5-g][1,8]naphthyridin-10(5H)-one
    参考文献:
    名称:
    Synthesis and antiproliferative activity of some novel benzo-fused imidazo[1,8]naphthyridinones
    摘要:
    A number of new substituted fused naphthyridinones has been prepared and their antiproliferative activity was evaluated against a panel of seven human tumor cell lines, including the variant MES-SA/Dx5, reported to be 100-fold resistant to doxorubicin. Certain derivatives exhibited interesting cytotoxic properties, possessing IC50 values in a low mu M range. (C) 2015 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2015.04.093
  • 作为产物:
    描述:
    2,6-二氯-3-硝基吡啶盐酸四(三苯基膦)钯 、 tin(II) chloride dihdyrate 、 磷酸caesium carbonate 、 sodium hydroxide 作用下, 以 1,4-二氧六环乙醇丙酮甲苯 为溶剂, 反应 26.33h, 生成 3-cyclopentyl-3H-benzo[b]imidazo[4,5-g][1,8]naphthyridin-10(5H)-one
    参考文献:
    名称:
    Synthesis and antiproliferative activity of some novel benzo-fused imidazo[1,8]naphthyridinones
    摘要:
    A number of new substituted fused naphthyridinones has been prepared and their antiproliferative activity was evaluated against a panel of seven human tumor cell lines, including the variant MES-SA/Dx5, reported to be 100-fold resistant to doxorubicin. Certain derivatives exhibited interesting cytotoxic properties, possessing IC50 values in a low mu M range. (C) 2015 Published by Elsevier Ltd.
    DOI:
    10.1016/j.bmcl.2015.04.093
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文献信息

  • Synthesis and antiproliferative activity of some novel benzo-fused imidazo[1,8]naphthyridinones
    作者:Vassiliki Giannouli、Ioannis K. Kostakis、Nicole Pouli、Panagiotis Marakos、Pinelopi Samara、Ourania Tsitsilonis
    DOI:10.1016/j.bmcl.2015.04.093
    日期:2015.7
    A number of new substituted fused naphthyridinones has been prepared and their antiproliferative activity was evaluated against a panel of seven human tumor cell lines, including the variant MES-SA/Dx5, reported to be 100-fold resistant to doxorubicin. Certain derivatives exhibited interesting cytotoxic properties, possessing IC50 values in a low mu M range. (C) 2015 Published by Elsevier Ltd.
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