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2-{2-[(tert-butoxycarbonyl)amino]ethyl}-6-({2-[(tert-butoxycarbonyl)amino]ethyl}amino)-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione | 1072879-21-0

中文名称
——
中文别名
——
英文名称
2-{2-[(tert-butoxycarbonyl)amino]ethyl}-6-({2-[(tert-butoxycarbonyl)amino]ethyl}amino)-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione
英文别名
tert-butyl N-[2-[6-[2-[(2-methylpropan-2-yl)oxycarbonylamino]ethylamino]-5-nitro-1,3-dioxobenzo[de]isoquinolin-2-yl]ethyl]carbamate
2-{2-[(tert-butoxycarbonyl)amino]ethyl}-6-({2-[(tert-butoxycarbonyl)amino]ethyl}amino)-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione化学式
CAS
1072879-21-0
化学式
C26H33N5O8
mdl
——
分子量
543.577
InChiKey
YMUAUKYIRVIPKI-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):
    3.9
  • 重原子数:
    39
  • 可旋转键数:
    11
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    172
  • 氢给体数:
    3
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    2-{2-[(tert-butoxycarbonyl)amino]ethyl}-6-({2-[(tert-butoxycarbonyl)amino]ethyl}amino)-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione盐酸 作用下, 以 1,4-二氧六环 为溶剂, 反应 3.0h, 以65%的产率得到2-[2-(amino)ethyl]-6-{[2-(amino)ethyl]amino}-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione dihydrochloride
    参考文献:
    名称:
    Design, synthesis, and biological evaluation of new mitonafide derivatives as potential antitumor drugs
    摘要:
    A series of potential DNA-binding antitumor agents, 2-[omega-(alkylamino) alkyl]-6-{[omega-(alkylamino) alkyl] amino}-1H-benzo[de] isoquinolin-1,3(2H)-diones and 1,7-bis{6-[(omega-(dimethylamino) alkyl) amino]-1,3dioxo-1H-benzo[de] isoquinolin-2(3H)-yl}-4-methyl-4-azaheptanes, have been prepared as mitonafide derivatives. Their DNA-binding ability and cytotoxic activity have been evaluated. Some of the target compounds have shown high DNA affinity as well as relevant cytotoxic properties. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.08.027
  • 作为产物:
    描述:
    N-叔丁氧羰基-1,2-乙二胺3-nitro-4-chloro-1,8-naphthalene dicarboxylic acid anhydride氯仿 为溶剂, 反应 3.0h, 以32%的产率得到2-{2-[(tert-butoxycarbonyl)amino]ethyl}-6-({2-[(tert-butoxycarbonyl)amino]ethyl}amino)-5-nitro-1H-benzo[de]isoquinoline-1,3(2H)-dione
    参考文献:
    名称:
    Design, synthesis, and biological evaluation of new mitonafide derivatives as potential antitumor drugs
    摘要:
    A series of potential DNA-binding antitumor agents, 2-[omega-(alkylamino) alkyl]-6-{[omega-(alkylamino) alkyl] amino}-1H-benzo[de] isoquinolin-1,3(2H)-diones and 1,7-bis{6-[(omega-(dimethylamino) alkyl) amino]-1,3dioxo-1H-benzo[de] isoquinolin-2(3H)-yl}-4-methyl-4-azaheptanes, have been prepared as mitonafide derivatives. Their DNA-binding ability and cytotoxic activity have been evaluated. Some of the target compounds have shown high DNA affinity as well as relevant cytotoxic properties. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.08.027
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文献信息

  • Design, synthesis, and biological evaluation of new mitonafide derivatives as potential antitumor drugs
    作者:Ippolito Antonini、Rosaria Volpini、Diego Dal Ben、Catia Lambertucci、Gloria Cristalli
    DOI:10.1016/j.bmc.2008.08.027
    日期:2008.9
    A series of potential DNA-binding antitumor agents, 2-[omega-(alkylamino) alkyl]-6-[omega-(alkylamino) alkyl] amino}-1H-benzo[de] isoquinolin-1,3(2H)-diones and 1,7-bis6-[(omega-(dimethylamino) alkyl) amino]-1,3dioxo-1H-benzo[de] isoquinolin-2(3H)-yl}-4-methyl-4-azaheptanes, have been prepared as mitonafide derivatives. Their DNA-binding ability and cytotoxic activity have been evaluated. Some of the target compounds have shown high DNA affinity as well as relevant cytotoxic properties. (C) 2008 Elsevier Ltd. All rights reserved.
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