sodium;(Z)-(2,6-dimethylpiperidin-1-yl)-oxido-oxidoiminoazanium | 1012338-77-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 哌啶类
• 英文名称: sodium;(Z)-(2,6-dimethylpiperidin-1-yl)-oxido-oxidoiminoazanium
• CAS: 1012338-77-0
• 化学式: C₇H₁₄N₃O₂*Na
• 分子量: 195.197
• InChiKey: YHXJCZKXUVAMAE-DQMXGCRQSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  -1.37
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  67.4
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  sodium;(Z)-(2,6-dimethylpiperidin-1-yl)-oxido-oxidoiminoazanium 、 2,4-二硝基氟苯 在 碳酸氢钠 作用下， 以 叔丁醇 为溶剂， 生成 (Z)-(2,6-dimethylpiperidin-1-yl)-(2,4-dinitrophenoxy)imino-oxidoazanium
  参考文献：
  名称：

  Synthesis and in vitro anti-leukemic activity of structural analogues of JS-K, an anti-cancer lead compound

  摘要：

  Structural analogues of JS-K, an anti-cancer lead compound, were prepared and their in vitro anti-leukemic activity was determined. The rate of nitric oxide release from the corresponding diazeniumdiolate anions did not appear to affect the anti-leukemic activity of the prodrug forms. Two compounds with potent inhibitory activity and a potentially favorable toxicological profile were identified. (C) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.12.044

文献信息

• Synthesis and in vitro anti-leukemic activity of structural analogues of JS-K, an anti-cancer lead compound
  作者：Harinath Chakrapani、Michael M. Goodblatt、Vidya Udupi、Swati Malaviya、Paul J. Shami、Larry K. Keefer、Joseph E. Saavedra

  DOI：10.1016/j.bmcl.2007.12.044

  日期：2008.2

  Structural analogues of JS-K, an anti-cancer lead compound, were prepared and their in vitro anti-leukemic activity was determined. The rate of nitric oxide release from the corresponding diazeniumdiolate anions did not appear to affect the anti-leukemic activity of the prodrug forms. Two compounds with potent inhibitory activity and a potentially favorable toxicological profile were identified. (C) 2007 Elsevier Ltd. All rights reserved.