4'-Chloro-5-methoxyflavone | 152038-81-8

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 黄酮类化合物
• 英文名称: 4'-Chloro-5-methoxyflavone
• 英文别名: 2-(4-chlorophenyl)-5-methoxy-4H-chromen-4-one；2-(4-chlorophenyl)-5-methoxychromen-4-one
• CAS: 152038-81-8
• 化学式: C₁₆H₁₁ClO₃
• 分子量: 286.715
• InChiKey: ZQEBKAYCIWBITP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 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：

  4'-Chloro-5-methoxyflavone 在 三溴化硼 作用下， 以 二氯甲烷 为溶剂， 生成 4'-Chloro-5-hydroxyflavone
  参考文献：
  名称：

  Synthesis and inhibitory activity against COX-2 catalyzed prostaglandin production of chrysin derivatives

  摘要：

  A series of chrysin derivatives were prepared and evaluated for their inhibitory activities of cyclooxygenase-2 catalyzed prostaglandin production. Chrysin derivatives were prepared from 2-hydroxyacetophenone, 2,4-dihydroxyacetophenone and 2,6-dihydroxyacetophenone in 2 to 4 steps, respectively. Methxoylated chrysin derivatives were converted to the corresponding hydroxylated chrysin derivatives by the reaction with BBr3 in good yields. The inhibitory activity of the chrysin derivatives against prostaglandin production from lipopolysaccharide-treated RAW 264.7 cells was measured. We found that chrysin derivatives with 3',4'-dichloro substituents (5e, 6e and 7e) exhibited good inhibitory activity of prostaglandin production. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.087
• 作为产物：
  描述：

  2,6-二羟基苯乙酮 在 氢氧化钾 、 碘 、 potassium carbonate 作用下， 以 甲醇 、 二甲基亚砜 、 丙酮 为溶剂， 生成 4'-Chloro-5-methoxyflavone
  参考文献：
  名称：

  Synthesis and inhibitory activity against COX-2 catalyzed prostaglandin production of chrysin derivatives

  摘要：

  A series of chrysin derivatives were prepared and evaluated for their inhibitory activities of cyclooxygenase-2 catalyzed prostaglandin production. Chrysin derivatives were prepared from 2-hydroxyacetophenone, 2,4-dihydroxyacetophenone and 2,6-dihydroxyacetophenone in 2 to 4 steps, respectively. Methxoylated chrysin derivatives were converted to the corresponding hydroxylated chrysin derivatives by the reaction with BBr3 in good yields. The inhibitory activity of the chrysin derivatives against prostaglandin production from lipopolysaccharide-treated RAW 264.7 cells was measured. We found that chrysin derivatives with 3',4'-dichloro substituents (5e, 6e and 7e) exhibited good inhibitory activity of prostaglandin production. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2003.12.087

文献信息

• A convenient large-scale synthesis of 5-methoxyflavone and its application to analog preparation
  作者：Jeffrey J. Ares、Pamela E. Outt、Sunil V. Kakodkar、Robert C. Buss、Jeffrey C. Geiger

  DOI：10.1021/jo00079a041

  日期：1993.12
• US5399584A
  申请人：——

  公开号：US5399584A

  公开（公告）日：1995-03-21
• Synthesis and inhibitory activity against COX-2 catalyzed prostaglandin production of chrysin derivatives
  作者：Tran Thanh Dao、Yeon Sook Chi、Jeongsoo Kim、Hyun Pyo Kim、Sanghee Kim、Haeil Park

  DOI：10.1016/j.bmcl.2003.12.087

  日期：2004.3

  A series of chrysin derivatives were prepared and evaluated for their inhibitory activities of cyclooxygenase-2 catalyzed prostaglandin production. Chrysin derivatives were prepared from 2-hydroxyacetophenone, 2,4-dihydroxyacetophenone and 2,6-dihydroxyacetophenone in 2 to 4 steps, respectively. Methxoylated chrysin derivatives were converted to the corresponding hydroxylated chrysin derivatives by the reaction with BBr3 in good yields. The inhibitory activity of the chrysin derivatives against prostaglandin production from lipopolysaccharide-treated RAW 264.7 cells was measured. We found that chrysin derivatives with 3',4'-dichloro substituents (5e, 6e and 7e) exhibited good inhibitory activity of prostaglandin production. (C) 2004 Elsevier Ltd. All rights reserved.