3-cyanobenzylselenocyanate | 1314654-19-7

• 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: 3-cyanobenzylselenocyanate
• 英文别名: (3-cyanophenyl)methyl selenocyanate
• CAS: 1314654-19-7
• 化学式: C₉H₆N₂Se
• 分子量: 221.12
• InChiKey: KQOSVPGGAFPZAC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.24
• 重原子数：
  12
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  47.6
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-cyanobenzylselenocyanate 在 sodium tetrahydroborate 作用下， 以 乙醇 为溶剂， 反应 2.0h， 以33%的产率得到3,3'-(diselanediylbis(methylene))dibenzonitrile
  参考文献：
  名称：

  Selenocyanates and diselenides: A new class of potent antileishmanial agents

  摘要：

  Thirty five selenocyanate and diselenide compounds were subjected to in vitro screening against Leishmania infantum promastigotes and the most active ones were also tested in an axenic amastigote model. In order to establish the selectivity indexes (SI) the cytotoxic effect of each compound was also assayed against Jurkat and THP-1 cell lines.Thirteen derivatives exhibit better IC50 values than miltefosine and edelfosine. Bis(4-aminophenyl) diselenide exhibits the best activity when assayed in infected macrophages and one of the lowest cytotoxic activities against the human cell lines tested, with SI values of 32 and 24 against Jurkat and THP-1 cells, respectively. This compound thus represents a new lead for further studies aimed at establishing its mechanism of action. (C) 2011 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2011.04.054
• 作为产物：
  描述：

  3-氰基苄基溴 在 potassium selenocyanate 作用下， 以 乙腈 为溶剂， 反应 3.0h， 生成 3-cyanobenzylselenocyanate
  参考文献：
  名称：

  一锅法从有机芥子酸酯中合成芳基和烷基的单氟甲基硒醚

  摘要：

  描述了使用KSeCN和ICFH 2通过一锅多步合成进行芳基和烷基卤化物单氟甲基硒化的第一种实际可行的方法。获得了良好的收率和广泛的官能团相容性。成功制备单氟甲基硒化的类药物化合物具有良好的实用性。该协议提供了许多新的单氟甲基硒醚，这将加速此类化合物在生命科学领域的使用。

  DOI：

  10.1002/adsc.201900480

文献信息

• Synthesis of Monofluoromethyl Selenoethers of Aryl and Alkyl from Organoselenocyanate via One‐Pot Reaction
  作者：Yuan Cao、Lvqi Jiang、Wenbin Yi

  DOI：10.1002/adsc.201900480

  日期：2019.9.17

  approach for the monofluoromethylselenolation of aryl and alkyl halides via one‐pot multistep synthesis using KSeCN and ICFH2 is described. Good yields and broad functional group compatibility were obtained. The successful preparation of monofluoromethylselenolated drug‐like compounds good practicability of this method. This protocol offered a number of new monofluoromethyl selenoethers, which would accelerate

  描述了使用KSeCN和ICFH 2通过一锅多步合成进行芳基和烷基卤化物单氟甲基硒化的第一种实际可行的方法。获得了良好的收率和广泛的官能团相容性。成功制备单氟甲基硒化的类药物化合物具有良好的实用性。该协议提供了许多新的单氟甲基硒醚，这将加速此类化合物在生命科学领域的使用。
• Selenocyanates and diselenides: A new class of potent antileishmanial agents
  作者：Daniel Plano、Ylenia Baquedano、David Moreno-Mateos、María Font、Antonio Jiménez-Ruiz、Juan Antonio Palop、Carmen Sanmartín

  DOI：10.1016/j.ejmech.2011.04.054

  日期：2011.8

  Thirty five selenocyanate and diselenide compounds were subjected to in vitro screening against Leishmania infantum promastigotes and the most active ones were also tested in an axenic amastigote model. In order to establish the selectivity indexes (SI) the cytotoxic effect of each compound was also assayed against Jurkat and THP-1 cell lines.Thirteen derivatives exhibit better IC50 values than miltefosine and edelfosine. Bis(4-aminophenyl) diselenide exhibits the best activity when assayed in infected macrophages and one of the lowest cytotoxic activities against the human cell lines tested, with SI values of 32 and 24 against Jurkat and THP-1 cells, respectively. This compound thus represents a new lead for further studies aimed at establishing its mechanism of action. (C) 2011 Elsevier Masson SAS. All rights reserved.