9-benzyl-3-methylene-1,5-bis(o-nitrobenzenesulfonyl)-1,5,9-triazacyclododecane

• 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: 9-benzyl-3-methylene-1,5-bis(o-nitrobenzenesulfonyl)-1,5,9-triazacyclododecane
• 英文别名: 9-Benzyl-3-methylidene-1,5-bis[(2-nitrophenyl)sulfonyl]-1,5,9-triazacyclododecane
• 化学式: C₂₉H₃₃N₅O₈S₂
• 分子量: 643.742
• InChiKey: QZVXZVPZRYAWKS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  44
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.31
• 拓扑面积：
  186
• 氢给体数：
  0
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  双(2-氰基乙基)胺 在 镍 sodium hydroxide 、 氢气 、 sodium hydride 、 sodium carbonate 、 sodium iodide 、 sodium chloride 作用下， 以 乙醚 、 乙醇 、 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 20.0~55.0 ℃ 、206.84 kPa 条件下， 反应 73.0h， 生成 9-benzyl-3-methylene-1,5-bis(o-nitrobenzenesulfonyl)-1,5,9-triazacyclododecane
  参考文献：
  名称：

  Synthesis and Structure−Activity Relationship Studies of CD4 Down-Modulating Cyclotriazadisulfonamide (CADA) Analogues

  摘要：

  HIV attachment via the CD4 receptor is an important target for developing novel approaches to HIV chemotherapy. Cyclotriazadisulfonamide (CADA) inhibits HIV at submicromolar levels by specifically down-modulating cell-surface and intracellular CD4. An effective five-step synthesis of CADA in 30% overall yield is reported. This synthesis has also been modified to produce more than 50 analogues. Many tail-group analogues have been made by removing the benzyl tail of CADA and replacing it with various alkyl, acyl, alkoxycarbonyl and aminocarbonyl substituents. A series of sidearm analogues, including two unsymmetrical compounds, have also been prepared by modifying the CADA synthesis, replacing the toluenesulfonyl sidearms with other sulfonyl groups. Testing 30 of these compounds in MT-4 cells shows a wide range of CD4 down-modulation potency, which correlates with ability to inhibit HIV-1. Three-dimensional quantitative structure-activity relationship (3D-QSAR) models were constructed using comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) approaches. The X-ray crystal structures of four compounds, including CADA, show the same major conformation of the central 12-membered ring. The solid-state structure of CADA was energy minimized and used to generate the remaining 29 structures, which were similarly minimized and aligned to produce the 3D-QSAR models. Both models indicate that steric bulk of the tail group, and, to a lesser extent, the sidearms mainly determine CD4 down-modulation potency in this series of compounds.

  DOI：

  10.1021/jm0582524

文献信息

• Synthesis and Structure−Activity Relationship Studies of CD4 Down-Modulating Cyclotriazadisulfonamide (CADA) Analogues
  作者：Thomas W. Bell、Sreenivasa Anugu、Patrick Bailey、Vincent J. Catalano、Kaka Dey、Michael G. B. Drew、Noah H. Duffy、Qi Jin、Meinrado F. Samala、Andrej Sodoma、William H. Welch、Dominique Schols、Kurt Vermeire

  DOI：10.1021/jm0582524

  日期：2006.2.1

  HIV attachment via the CD4 receptor is an important target for developing novel approaches to HIV chemotherapy. Cyclotriazadisulfonamide (CADA) inhibits HIV at submicromolar levels by specifically down-modulating cell-surface and intracellular CD4. An effective five-step synthesis of CADA in 30% overall yield is reported. This synthesis has also been modified to produce more than 50 analogues. Many tail-group analogues have been made by removing the benzyl tail of CADA and replacing it with various alkyl, acyl, alkoxycarbonyl and aminocarbonyl substituents. A series of sidearm analogues, including two unsymmetrical compounds, have also been prepared by modifying the CADA synthesis, replacing the toluenesulfonyl sidearms with other sulfonyl groups. Testing 30 of these compounds in MT-4 cells shows a wide range of CD4 down-modulation potency, which correlates with ability to inhibit HIV-1. Three-dimensional quantitative structure-activity relationship (3D-QSAR) models were constructed using comparative molecular field analysis (CoMFA) and comparative molecular similarity indices analysis (CoMSIA) approaches. The X-ray crystal structures of four compounds, including CADA, show the same major conformation of the central 12-membered ring. The solid-state structure of CADA was energy minimized and used to generate the remaining 29 structures, which were similarly minimized and aligned to produce the 3D-QSAR models. Both models indicate that steric bulk of the tail group, and, to a lesser extent, the sidearms mainly determine CD4 down-modulation potency in this series of compounds.