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7-methoxy-8-{3-[(5-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)-2-methoxyphenyl)oxy]propyloxy}-(11aS)-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one | 1251485-19-4

中文名称
——
中文别名
——
英文名称
7-methoxy-8-{3-[(5-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)-2-methoxyphenyl)oxy]propyloxy}-(11aS)-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one
英文别名
(6aS)-3-[3-[5-[5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl]-2-methoxyphenoxy]propoxy]-2-methoxy-6a,7,8,9-tetrahydropyrrolo[2,1-c][1,4]benzodiazepin-11-one
7-methoxy-8-{3-[(5-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)-2-methoxyphenyl)oxy]propyloxy}-(11aS)-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one化学式
CAS
1251485-19-4
化学式
C31H29FN4O6
mdl
——
分子量
572.593
InChiKey
MXHKMODFZWREML-QFIPXVFZSA-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):
    4.3
  • 重原子数:
    42
  • 可旋转键数:
    10
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    109
  • 氢给体数:
    0
  • 氢受体数:
    10

反应信息

  • 作为产物:
    描述:
    calcium carbonate 、 mercury dichloride 作用下, 以 乙腈 为溶剂, 反应 12.0h, 以332 mg的产率得到7-methoxy-8-{3-[(5-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)-2-methoxyphenyl)oxy]propyloxy}-(11aS)-1,2,3,11a-tetrahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one
    参考文献:
    名称:
    Synthesis, anticancer activity and mitochondrial mediated apoptosis inducing ability of 2,5-diaryloxadiazole–pyrrolobenzodiazepine conjugates
    摘要:
    A series of 2,5-diaryloxadiazole linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates have been prepared and evaluated for their anticancer activity. These conjugates have shown promising activity with GI(50) values ranging from < 0.1 to 0.29 mu M. It is observed that some of these conjugates particularly 4a, 4d, 4i and 4l exhibit significant anticancer activity. Some detailed biological assays relating to the cell cycle aspects associated to Bax and caspases have been examined with a view to understand the mechanism of action of these conjugates. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.07.067
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文献信息

  • Synthesis, anticancer activity and mitochondrial mediated apoptosis inducing ability of 2,5-diaryloxadiazole–pyrrolobenzodiazepine conjugates
    作者:Ahmed Kamal、D. Dastagiri、M. Janaki Ramaiah、E. Vijaya Bharathi、J. Surendranadha Reddy、G. Balakishan、Pranjal Sarma、S.N.C.V.L. Pushpavalli、Manika Pal-Bhadra、Aarti Juvekar、Subrata Sen、Surekha Zingde
    DOI:10.1016/j.bmc.2010.07.067
    日期:2010.9
    A series of 2,5-diaryloxadiazole linked pyrrolo[2,1-c][1,4]benzodiazepine conjugates have been prepared and evaluated for their anticancer activity. These conjugates have shown promising activity with GI(50) values ranging from < 0.1 to 0.29 mu M. It is observed that some of these conjugates particularly 4a, 4d, 4i and 4l exhibit significant anticancer activity. Some detailed biological assays relating to the cell cycle aspects associated to Bax and caspases have been examined with a view to understand the mechanism of action of these conjugates. (c) 2010 Elsevier Ltd. All rights reserved.
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