N'-hydroxy-4-[4-{3-[4-(N'-hydroxycarbamimidoyl)phenylsulfonyl]-5,5-diphenyl-4,5-dihydrofuran-2-yl}styryl]benzimidamide | 1253695-89-4

• 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: N'-hydroxy-4-[4-{3-[4-(N'-hydroxycarbamimidoyl)phenylsulfonyl]-5,5-diphenyl-4,5-dihydrofuran-2-yl}styryl]benzimidamide
• CAS: 1253695-89-4
• 化学式: C₃₈H₃₂N₄O₅S
• 分子量: 656.762
• InChiKey: ACMASRJLPQSCON-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.55
• 重原子数：
  48.0
• 可旋转键数：
  9.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.05
• 拓扑面积：
  160.59
• 氢给体数：
  4.0
• 氢受体数：
  7.0

反应信息

• 作为产物：
  描述：

  4-{4-[3-(4-cyanophenylsulfonyl)-5,5-diphenyl-4,5-dihydrofuran-2-yl]styryl}benzonitrile 在 盐酸羟胺 、 potassium tert-butylate 作用下， 以 二甲基亚砜 为溶剂， 反应 12.0h， 以70%的产率得到N'-hydroxy-4-[4-{3-[4-(N'-hydroxycarbamimidoyl)phenylsulfonyl]-5,5-diphenyl-4,5-dihydrofuran-2-yl}styryl]benzimidamide
  参考文献：
  名称：

  Synthesis and evaluation of original amidoximes as antileishmanial agents

  摘要：

  An original series of amidoxime derivatives was synthesized using manganese(III) acetate, Buchwald-Hartwig and Heck reactions. Two amidoximes (39 and 52) showed interesting in vitro activities toward Leishmania donovani promastigotes, exhibiting 8.3 and 8.8 mu M IC50 values. Moreover, the cytotoxicity of these compounds was evaluated on human THP1 cells, giving access to the corresponding selectivity index. Among the 25 tested compounds, amidoximes 38 and 39 and diamidoximes 50 and 52 exhibited a better selectivity index than pentamidine used as a drug compound reference. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.06.099