cis-6-(3,5-dimethoxystyryl)-3-(4-methoxyphenyl)coumarin | 1387531-34-1

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二芳基庚烷
• 英文名称: cis-6-(3,5-dimethoxystyryl)-3-(4-methoxyphenyl)coumarin
• 英文别名: cis-6-(3,5-Dimethoxystyryl)-3-(4-methoxyphenyl)coumarin；6-[(Z)-2-(3,5-dimethoxyphenyl)ethenyl]-3-(4-methoxyphenyl)chromen-2-one
• CAS: 1387531-34-1
• 化学式: C₂₆H₂₂O₅
• 分子量: 414.458
• InChiKey: CIULIGYDTHEAQI-PLNGDYQASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.7
• 重原子数：
  31
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  54
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  3-(4-methoxyphenyl)-6-methyl-2H-chromen-2-one 在 N-溴代丁二酰亚胺(NBS) 、 溶剂黄146 、 sodium hydroxide 、 过氧化苯甲酰 作用下， 以 二氯甲烷 、 苯 为溶剂， 反应 10.67h， 生成 cis-6-(3,5-dimethoxystyryl)-3-(4-methoxyphenyl)coumarin 、 trans-6-(3,5-dimethoxystyryl)-3-(4-methoxyphenyl)coumarin
  参考文献：
  名称：

  Synthesis and biological evaluation of resveratrol–coumarin hybrid compounds as potential antitumor agents

  摘要：

  Eighteen resveratrol-coumarin hybrid compounds (6 or 7-styryl-3-phenylcoumarin) were designed, synthesized and thirteen compounds were evaluated for their antitumor activities against MCF-7, HCT-28, and K562 tumor cell lines. Among them, compounds 2Z, 2E, 5E, and 7E showed varying degrees of growth inhibition of the above cell lines (IC50: 3.78-19.16 mu mol/L). On the basis of the biological results, structure-activity relationships were obtained and discussed.

  DOI：

  10.1007/s00044-012-0159-y

文献信息

• Synthesis and biological evaluation of resveratrol–coumarin hybrid compounds as potential antitumor agents
  作者：Wei Shen、Jianfeng Mao、Juan Sun、Minjie Sun、Can Zhang

  DOI：10.1007/s00044-012-0159-y

  日期：2013.4

  Eighteen resveratrol-coumarin hybrid compounds (6 or 7-styryl-3-phenylcoumarin) were designed, synthesized and thirteen compounds were evaluated for their antitumor activities against MCF-7, HCT-28, and K562 tumor cell lines. Among them, compounds 2Z, 2E, 5E, and 7E showed varying degrees of growth inhibition of the above cell lines (IC50: 3.78-19.16 mu mol/L). On the basis of the biological results, structure-activity relationships were obtained and discussed.