8-ethoxy-3-phenylcoumarin | 1309856-39-0

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 异黄酮类化合物
• 英文名称: 8-ethoxy-3-phenylcoumarin
• 英文别名: 8-ethoxy-3-phenylchromen-2-one
• CAS: 1309856-39-0
• 化学式: C₁₇H₁₄O₃
• 分子量: 266.296
• InChiKey: JWPFCIXQOFVAHQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  20
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  8-ethoxy-3-phenylcoumarin 在 氢碘酸 、 乙酸酐 、 溶剂黄146 作用下， 反应 3.0h， 以64%的产率得到8-hydroxy-3-phenylcoumarin
  参考文献：
  名称：

  New halogenated phenylcoumarins as tyrosinase inhibitors

  摘要：

  With the aim to find out structural features for the tyrosinase inhibitory activity, in the present communication we report the synthesis and pharmacological evaluation of a new series of phenylcoumarin derivatives with different number of hydroxyl or ether groups and bromo substituent in the scaffold. The synthesized compounds 5-12 were evaluated as mushroom tyrosinase inhibitors showing, two of them, lower IC50 than the umbelliferone. Compound 12 (IC50 = 215 mu M) is the best tyrosinase inhibitor of this series. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.04.012
• 作为产物：
  描述：

  苯乙酸 、 3-乙氧基水杨醛 在 N,N'-二环己基碳二亚胺 作用下， 以 二甲基亚砜 为溶剂， 反应 24.0h， 生成 8-ethoxy-3-phenylcoumarin
  参考文献：
  名称：

  Structure-Based Optimization of Coumarin hA₃ Adenosine Receptor Antagonists

  摘要：

  Adenosine receptors participate in many physiological functions. Molecules that may selectively interact with one of the receptors are favorable multifunctional chemical entities to treat or decelerate the evolution of different diseases. 3-Arylcoumarins have already been studied as neuroprotective agents by our group. Here, differently 8-substituted 3-arylcoumarins are complementarily studied as ligands of adenosine receptors, performing radioligand binding assays. Among the synthesized compounds, selective A(3) receptor antagonists were found. 3-(4-Bromophenyl)-8-hydroxycoumarin (compound 4) displayed the highest potency and selectivity as A(3) receptor antagonist (K-i = 258 nM). An analysis of its X-ray diffraction provided detailed information on its structure. Further evaluation of a selected series of compounds indicated that it is the nature and position of the substituents that determine their activity and selectivity. Theoretical modeling calculations corroborate and explain the experimental data, suggesting this novel scaffold can be involved in the generation of candidates as multitarget drugs.

  DOI：

  10.1021/acs.jmedchem.9b01572