| 888223-85-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• CAS: 888223-85-6
• 化学式: C₅₄H₅₃F₃N₆O₁₁
• 分子量: 1019.04
• InChiKey: UYCQVKYRAUBPRZ-UFCNIINJSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.74
• 重原子数：
  74.0
• 可旋转键数：
  21.0
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  219.62
• 氢给体数：
  5.0
• 氢受体数：
  14.0

反应信息

• 作为反应物：
  描述：

  、 2-氰乙基N,N-二异丙基氯亚磷酰胺 生成
  参考文献：
  名称：

  Novel fluorescent oligoDNA probe bearing a multi-conjugated nucleoside with a fluorophore and a non-fluorescent intercalator as a quencher

  摘要：

  A set of 15mer linear oligoDNA probes bearing a modified nucleoside conjugated with a polyamine/fluorescein/anthraquinone reporting moiety were synthesized. In a single-stranded form, the fluorescence generated by the excitation of fluorescein was efficiently quenched, while marked recovery of the fluorescence was observed when the probes formed duplexes with the fully complementary strand. (C) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.02.016
• 作为产物：
  描述：

  1-<2-ethylamino>anthraquinone 以 N,N-二甲基乙酰胺 为溶剂， 生成
  参考文献：
  名称：

  Novel fluorescent oligoDNA probe bearing a multi-conjugated nucleoside with a fluorophore and a non-fluorescent intercalator as a quencher

  摘要：

  A set of 15mer linear oligoDNA probes bearing a modified nucleoside conjugated with a polyamine/fluorescein/anthraquinone reporting moiety were synthesized. In a single-stranded form, the fluorescence generated by the excitation of fluorescein was efficiently quenched, while marked recovery of the fluorescence was observed when the probes formed duplexes with the fully complementary strand. (C) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2006.02.016