| 1150591-83-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• CAS: 1150591-83-5
• 化学式: C₃₃H₄₀ClN₃O₄
• 分子量: 578.151
• InChiKey: PUIHSUKXZWLZTN-UHFFFAOYSA-N

物化性质

• 密度：
  1.33±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  7.1
• 重原子数：
  41
• 可旋转键数：
  7
• 环数：
  9.0
• sp3杂化的碳原子比例：
  0.61
• 拓扑面积：
  73.9
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  adamantane-2-spiro-3'-8'-oxo-1',2',4'-trioxaspiro[4,5]decane 、 N¹-(6-chloro-2-methoxy-acridin-9-yl)-propane-1,3-diamine 在 三乙酰氧基硼氢化钠 作用下， 以 二氯甲烷 为溶剂， 以49%的产率得到
  参考文献：
  名称：

  Semi-synthetic and synthetic 1,2,4-trioxaquines and 1,2,4-trioxolaquines: synthesis, preliminary SAR and comparison with acridine endoperoxide conjugates

  摘要：

  A novel series of semi-synthetic trioxaquines and synthetic trioxolaquines were prepared, in moderate to good yields. Antimalarial activity was evaluated against both the chloroquine-sensitive 3D7 and resistant K1 strain of Plasmodium falciparum and both series of compounds were shown to be active in the low nanomolar range. For comparison the corresponding 9-amino acridine analogues were also prepared and shown to have low nanomolar activity like their quinoline counterparts. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.02.013

文献信息

• Semi-synthetic and synthetic 1,2,4-trioxaquines and 1,2,4-trioxolaquines: synthesis, preliminary SAR and comparison with acridine endoperoxide conjugates
  作者：Nuna C.P. Araújo、Victoria Barton、Michael Jones、Paul A. Stocks、Stephen A. Ward、Jill Davies、Patrick G. Bray、Alison E. Shone、Maria L.S. Cristiano、Paul M. O’Neill

  DOI：10.1016/j.bmcl.2009.02.013

  日期：2009.4

  A novel series of semi-synthetic trioxaquines and synthetic trioxolaquines were prepared, in moderate to good yields. Antimalarial activity was evaluated against both the chloroquine-sensitive 3D7 and resistant K1 strain of Plasmodium falciparum and both series of compounds were shown to be active in the low nanomolar range. For comparison the corresponding 9-amino acridine analogues were also prepared and shown to have low nanomolar activity like their quinoline counterparts. (C) 2009 Elsevier Ltd. All rights reserved.