1-[1-(N,N-dimethylamino)diazen-1-ium-1,2-diol-2-ato]-2,4-dinitro-5-{[(4-n-butoxycarbonyl)piperazin-1-yl]diazen-1-ium-1,2-diol-2-ato}benzene | 1093077-84-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: 1-[1-(N,N-dimethylamino)diazen-1-ium-1,2-diol-2-ato]-2,4-dinitro-5-{[(4-n-butoxycarbonyl)piperazin-1-yl]diazen-1-ium-1,2-diol-2-ato}benzene
• 英文别名: (4-butoxycarbonylpiperazin-1-yl)-[5-[[dimethylamino(oxido)azaniumylidene]amino]oxy-2,4-dinitrophenoxy]imino-oxidoazanium
• CAS: 1093077-84-9
• 化学式: C₁₇H₂₅N₉O₁₀
• 分子量: 515.44
• InChiKey: RCUXRRAEWDAYHE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  36
• 可旋转键数：
  10
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.59
• 拓扑面积：
  228
• 氢给体数：
  0
• 氢受体数：
  14

反应信息

• 作为产物：
  描述：

  sodium 1-[4-(n-butoxycarbonyl)piperazin-1-yl]diazen-1-ium-1,2-diolate 、 O²-(2,4-dinitro-5-fluorophenyl) 1-(N,N-dimethylamino)diazen-1-ium-1,2-diolate 以 丙酮 为溶剂， 以93%的产率得到1-[1-(N,N-dimethylamino)diazen-1-ium-1,2-diol-2-ato]-2,4-dinitro-5-{[(4-n-butoxycarbonyl)piperazin-1-yl]diazen-1-ium-1,2-diol-2-ato}benzene
  参考文献：
  名称：

  Aryl Bis(diazeniumdiolates): Potent Inducers of S-Glutathionylation of Cellular Proteins and Their in Vitro Antiproliferative Activities

  摘要：

  A number of bis(diazeniumdiolates) that we designed to release up to 4 mol of nitric oxide (NO) and that are structural analogues of the NO prodrug and anticancer lead compound O-2-{2,4-dinitro-5-[4-(N-methylamino)benzoyloxy]phenyl} 1-(N,N-dimethylamino)diazen-1-ium-1,2-diolate (PABA/NO) were synthesized and studied. A majority of these compounds yielded higher levels of NO, were better inhibitors of proliferation of a number of cancer cell lines, and more rapidly induced substantially increased levels of S-glutathionylation of cellular proteins in comparison with PABA/NO. In most cases, the antiproliferative activity and extents of S-glutathionylation correlated well with levels of intracellular NO release. We report bis(diazeniumdiolates) to be a class of S-glutathionylating agents with potent antiproliferative and S-glutathionylating activity.

  DOI：

  10.1021/jm800831y