| 1447139-00-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• CAS: 1447139-00-5
• 化学式: C₂₂H₂₆INO₃Si
• 分子量: 507.443
• InChiKey: ABVIZJXNASLCLB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.25
• 重原子数：
  28.0
• 可旋转键数：
  6.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  63.23
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  在 copper(l) iodide 、 四丁基氟化铵 、 caesium carbonate 、 对甲苯磺酸 作用下， 以 四氢呋喃 、 邻二氯苯 、 苯 为溶剂， 反应 24.5h， 生成
  参考文献：
  名称：

  Structure–activity-relationship studies on dihydrofuran-fused perhydrophenanthrenes as an anti-Alzheimer’s disease agent

  摘要：

  As an extended study on development of anti-Alzheimer's disease agent, we newly synthesized various dihydrofuran-fused perhydrophenanthrenes via o-quinodimethane chemistry. This study revealed that the introduction of carbon side-chain on 8-position or removal of the acetal moiety on 3-position arose a cytotoxicity on rat cortical neurons. On the other hand, the ethereal or thio-ethereal substituent on 8-position enhanced the elongation effect on A beta-damaged neurons. The necessity of the cyano group on 10b position was also proved in this structure-activity-relationship study. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2013.05.059
• 作为产物：
  描述：

  在 重铬酸吡啶 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 以74%的产率得到
  参考文献：
  名称：

  Structure–activity-relationship studies on dihydrofuran-fused perhydrophenanthrenes as an anti-Alzheimer’s disease agent

  摘要：

  As an extended study on development of anti-Alzheimer's disease agent, we newly synthesized various dihydrofuran-fused perhydrophenanthrenes via o-quinodimethane chemistry. This study revealed that the introduction of carbon side-chain on 8-position or removal of the acetal moiety on 3-position arose a cytotoxicity on rat cortical neurons. On the other hand, the ethereal or thio-ethereal substituent on 8-position enhanced the elongation effect on A beta-damaged neurons. The necessity of the cyano group on 10b position was also proved in this structure-activity-relationship study. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2013.05.059