1,3,5-benzenetricarbonic acid tris-4-aminobutylamide | 777055-97-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 1,3,5-benzenetricarbonic acid tris-4-aminobutylamide
• 英文别名: 1-N,3-N,5-N-tris(4-aminobutyl)benzene-1,3,5-tricarboxamide
• CAS: 777055-97-7
• 化学式: C₂₁H₃₆N₆O₃
• 分子量: 420.555
• InChiKey: BQWMERDVPIJAJM-UHFFFAOYSA-N

物化性质

• 沸点：
  714.6±60.0 °C(Predicted)
• 密度：
  1.136±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.9
• 重原子数：
  30
• 可旋转键数：
  15
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  165
• 氢给体数：
  6
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  1,1-双(二乙氧基磷酰基)乙烯 、 1,3,5-benzenetricarbonic acid tris-4-aminobutylamide 以 N,N-二甲基甲酰胺 为溶剂， 反应 48.0h， 生成
  参考文献：
  名称：

  Bisphosphonate sequestering agents. Synthesis and preliminary evaluation for in vitro and in vivo uranium(VI) chelation

  摘要：

  A library of bisphosphonate-based ligands was prepared using solution-phase parallel synthesis and tested for its uranium-binding properties. With the help of a screening method, based on a chromophoric complex displacement procedure, 23 dipodal and tripodal chelates bearing bisphosphonate chelating functions were found to display very high affinity for the uranyl ion and were selected for evaluation of their in vivo uranyl-removal efficacy. Among them, 11 ligands induced a huge modification of the uranyl biodistribution by deviating the metal from kidney and bones to liver. Among the other ligands, the most potent was the dipodal bisphosphonate 3C which reduced the retention of uranyl and increased its excretion by around 10% of the injected metal. (C) 2008 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2008.01.018
• 作为产物：
  描述：

  N-叔丁氧羰基-1,4-丁二胺 、 均苯三甲酸 在 1-羟基苯并三唑 、 1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 8.0h， 以100%的产率得到1,3,5-benzenetricarbonic acid tris-4-aminobutylamide
  参考文献：
  名称：

  Design and Synthesis of C₃-Symmetric Lewis^X Antigen

  摘要：

  [GRAPHICS]C-3-Symmetric glycoconjugates carrying three equivalent Lewis(x) antigens or beta-lactosides were synthesized from p-nitrophenyl glycosides and trimesic acid via regio- and stereocontrolled glycosylation reactions. An H-1 NMR study has shown that the C-3-symmetric glycoconjugates soluble in water provide useful probes to investigate the Ca2+-dependent Lewis(x)-Lewis(x) association.

  DOI：

  10.1021/ol0351293

文献信息

• Bisphosphonate sequestering agents. Synthesis and preliminary evaluation for in vitro and in vivo uranium(VI) chelation
  作者：Marcin Sawicki、Delphine Lecerclé、Gérard Grillon、Béatrice Le Gall、Anne-Laure Sérandour、Jean-Luc Poncy、Théodorine Bailly、Ramon Burgada、Marc Lecouvey、Vincent Challeix、Antoine Leydier、Stephane Pellet-Rostaing、Eric Ansoborlo、Frédéric Taran

  DOI：10.1016/j.ejmech.2008.01.018

  日期：2008.12

  A library of bisphosphonate-based ligands was prepared using solution-phase parallel synthesis and tested for its uranium-binding properties. With the help of a screening method, based on a chromophoric complex displacement procedure, 23 dipodal and tripodal chelates bearing bisphosphonate chelating functions were found to display very high affinity for the uranyl ion and were selected for evaluation of their in vivo uranyl-removal efficacy. Among them, 11 ligands induced a huge modification of the uranyl biodistribution by deviating the metal from kidney and bones to liver. Among the other ligands, the most potent was the dipodal bisphosphonate 3C which reduced the retention of uranyl and increased its excretion by around 10% of the injected metal. (C) 2008 Elsevier Masson SAS. All rights reserved.
• Design and Synthesis of <i>C</i>₃-Symmetric Lewis^X Antigen
  作者：Yoshihiro Nishida、Tomoaki Tsurumi、Kenji Sasaki、Kenta Watanabe、Hirofumi Dohi、Kazukiyo Kobayashi

  DOI：10.1021/ol0351293

  日期：2003.10.1

  [GRAPHICS]C-3-Symmetric glycoconjugates carrying three equivalent Lewis(x) antigens or beta-lactosides were synthesized from p-nitrophenyl glycosides and trimesic acid via regio- and stereocontrolled glycosylation reactions. An H-1 NMR study has shown that the C-3-symmetric glycoconjugates soluble in water provide useful probes to investigate the Ca2+-dependent Lewis(x)-Lewis(x) association.