10beta-Phenyl-triazolylartemisinin | 1119668-72-2

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 异戊烯醇脂质
• 英文名称: 10beta-Phenyl-triazolylartemisinin
• 英文别名: 4-phenyl-1-[(1R,4S,5R,8S,9R,10S,12R,13R)-1,5,9-trimethyl-11,14,15,16-tetraoxatetracyclo[10.3.1.04,13.08,13]hexadecan-10-yl]triazole
• CAS: 1119668-72-2
• 化学式: C₂₃H₂₉N₃O₄
• 分子量: 411.501
• InChiKey: MRWSNVXGNLTHER-RGFASOFISA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  30
• 可旋转键数：
  2
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  67.6
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  9β,10β-azidoartemisinin 、 苯乙炔 在 copper(II) sulfate 、 sodium ascorbate 作用下， 以 二氯甲烷 、 水 为溶剂， 反应 48.0h， 以20%的产率得到10beta-Phenyl-triazolylartemisinin
  参考文献：
  名称：

  Synthesis of 10-substituted triazolyl artemisinins possessing anticancer activity via Huisgen 1,3-dipolar cylcoaddition

  摘要：

  Most of the 10-substituted triazolylartemisinin synthesized via the Huisgen 1,3-dipolar cylcoaddition of diastereomeric 10-azidoartemisinin (5, 6, and 7) with various alkynes (a-h) exhibit strong growth inhibition activity, even at sub-micromolar concentrations, against various cancer cell lines such as DLD-1, U-87, Hela, SiHa, A172, and B16. In particular, 10b and 10f showed a highly strong cytotoxicity. (C) 2008 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmcl.2008.11.067

文献信息

• Synthesis of 10-substituted triazolyl artemisinins possessing anticancer activity via Huisgen 1,3-dipolar cylcoaddition
  作者：Sungsik Cho、Sangtae Oh、Yumi Um、Ji-Hee Jung、Jungyeob Ham、Woon-Seob Shin、Seokjoon Lee

  DOI：10.1016/j.bmcl.2008.11.067

  日期：2009.1

  Most of the 10-substituted triazolylartemisinin synthesized via the Huisgen 1,3-dipolar cylcoaddition of diastereomeric 10-azidoartemisinin (5, 6, and 7) with various alkynes (a-h) exhibit strong growth inhibition activity, even at sub-micromolar concentrations, against various cancer cell lines such as DLD-1, U-87, Hela, SiHa, A172, and B16. In particular, 10b and 10f showed a highly strong cytotoxicity. (C) 2008 Published by Elsevier Ltd.