(E)-3-(4-(dimethylamino)phenyl)-1-(4-(((E)-3-iodoallyl)oxy)phenyl)prop-2-en-1-one | 1607465-96-2

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 直链 1,3-二芳基丙烷
• 英文名称: (E)-3-(4-(dimethylamino)phenyl)-1-(4-(((E)-3-iodoallyl)oxy)phenyl)prop-2-en-1-one
• 英文别名: (E)-3-[4-(dimethylamino)phenyl]-1-[4-[(E)-3-iodoprop-2-enoxy]phenyl]prop-2-en-1-one
• CAS: 1607465-96-2
• 化学式: C₂₀H₂₀INO₂
• 分子量: 433.289
• InChiKey: ZBKNLBQFTYHMEN-HOWOQDSESA-N

物化性质

• 沸点：
  544.839±50.00 °C(Press: 760.00 Torr)(predicted)
• 密度：
  1.458±0.06 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  24
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  29.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  (E)-3-(4-(dimethylamino)phenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one 在 碘 、 sodium hydride 作用下， 以 氯仿 、 N,N-二甲基甲酰胺 为溶剂， 反应 4.58h， 生成 (E)-3-(4-(dimethylamino)phenyl)-1-(4-(((E)-3-iodoallyl)oxy)phenyl)prop-2-en-1-one
  参考文献：
  名称：

  Synthesis and evaluation of ethyleneoxylated and allyloxylated chalcone derivatives for imaging of amyloid β plaques by SPECT

  摘要：

  We report radioiodinated chalcone derivatives as new SPECT imaging probes for amyloid beta (A beta) plaques. The monoethyleneoxy derivative 2 and allyloxy derivative 8 showed a high affinity for A beta(1-42) aggregates with K-i values of 24 and 4.5 nM, respectively. Fluorescent imaging demonstrated that 2 and 8 clearly stained thioflavin-S positive A beta plaques in the brain sections of Tg2576 transgenic mice. In vitro autoradiography revealed that [I-125]2 displayed no clear accumulation toward A beta plaques in the brain sections of Tg2576 mice, whereas the accumulation pattern of [I-125]8 matched with the presence of A beta plaques both in the brain sections of Tg2576 mice and an AD patient. In biodistribution studies using normal mice, [I-125]2 showed preferable in vivo pharmacokinetics (4.82%ID/g at 2 min and 0.45%ID/g at 60 min), while [I-125]8 showed only a modest brain uptake (1.62%ID/g at 2 min) with slow clearance (0.56%ID/g at 60 min). [I-125]8 showed prospective binding properties for A beta plaques, although further structural modifications are needed to improve the blood brain barrier permeability and washout from brain. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2014.03.032