3-[2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propyloleate | 1027369-38-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 2-芳基苯并呋喃类黄酮
• 英文名称: 3-[2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propyloleate
• 英文别名: egonol oleate；3-[2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propyl (Z)-octadec-9-enoate
• CAS: 1027369-38-5
• 化学式: C₃₇H₅₀O₆
• 分子量: 590.8
• InChiKey: GVZWPCDBHBSBHJ-KHPPLWFESA-N

物化性质

• 沸点：
  686.1±55.0 °C(Predicted)
• 密度：
  1.073±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  11.8
• 重原子数：
  43
• 可旋转键数：
  22
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  67.1
• 氢给体数：
  0
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  3-[2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propyloleate 在 臭氧 、 二甲基硫 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 12.0h， 生成 [2-Formyl-6-methoxy-4-[3-(9-oxononanoyloxy)propyl]phenyl] 1,3-benzodioxole-5-carboxylate
  参考文献：
  名称：

  Benzofurans from Styrax agrestis As Acetylcholinesterase Inhibitors: Structure–Activity Relationships and Molecular Modeling Studies

  摘要：

  An extract of Styrax agrestis fruits, collected in Vietnam, significantly inhibited acetylcholinesterase (AChE) in vitro. Bioassay-guided fractionation revealed three new egonol-type benzofurans: egonol-9(Z),12(Z) linoleate (1), 7-demethoxy-egonol-9(Z),12(Z) linoleate (2), and 7-demethoxyegonol oleate (4). Ten known egonol-type benzofurans were also isolated (3, 5, 6-13). In order to better understand structure activity relationships in this series, egonol derivatives 14-19 were prepared by chemical modifications and evaluated for their inhibition of AChE, butyrylcholinesterase (BChE), and AChE-induced A beta aggregation. Compounds 1-4 were the most potent inhibitors of the series, which exhibited inhibitory activity against AChE (IC50 1.4-3.1 mu M) and, for 1, A beta aggregation (77.6%). Molecular docking studies were also performed to investigate interaction of these compounds with the active site of AChE.

  DOI：

  10.1021/np200308j
• 作为产物：
  描述：

  油酸 、 5-(3-羟基丙基)-7-甲氧基-2-(3,4-亚甲二氧基苯基)苯并呋喃 以 吡啶 、 二氯甲烷 为溶剂， 反应 72.0h， 以5.57%的产率得到3-[2-(1,3-benzodioxol-5-yl)-7-methoxy-1-benzofuran-5-yl]propyloleate
  参考文献：
  名称：

  松香酚衍生物的合成和抗菌活性。

  摘要：

  3-苯并二恶唑-5-基）-7-甲氧基-1-苯并呋喃-5-基]丙基苯甲酸酯10，5- [3''-羟丙基] -7-甲氧基-3-硝基-2-（3'，4'报道了-亚甲基二氧苯基）苯并呋喃11及其对金黄色葡萄球菌，枯草芽孢杆菌，白色念珠菌和大肠杆菌的抗菌活性。从麦草的种子中分离出原料烯醇5- [3''-（羟基）丙基] -7-甲氧基-2-（3'，4'亚甲基二氧苯基）苯并呋喃。这些化合物的结构解析（1-使用1D（（1）H，（13）C），2D NMR（HMBC，HMQC，COSY）和LCMS光谱数据建立11）。蛋黄酚和一些合成的新化合物对金黄色葡萄球菌，枯草芽孢杆菌，白色念珠菌和大肠杆菌显示相似的抗菌活性和MIC值，而其他新衍生物对金黄色葡萄球菌，枯草芽孢杆菌，C。显示出不同的活性。

  DOI：

  10.1016/j.bmc.2008.02.057

文献信息

• Synthesis and antibacterial activity of egonol derivatives
  作者：Safiye Emirdağ Öztürk、Yurdanur Akgül、Hüseyin Anıl

  DOI：10.1016/j.bmc.2008.02.057

  日期：2008.4

  4'methylenedioxyphenyl)benzofuran was isolated from seeds of Styrax officinalis L. The structural elucidication of these compounds (1-11) was established using 1D ((1)H, (13)C), 2D NMR (HMBC, HMQC, COSY) and LCMS spectroscopic data. While egonol and some synthesised new compounds show similar antibacterial activity and MIC values against S. aureus, B. subtilis, C. albicans and E. coli, other new derivatives show

  3-苯并二恶唑-5-基）-7-甲氧基-1-苯并呋喃-5-基]丙基苯甲酸酯10，5- [3''-羟丙基] -7-甲氧基-3-硝基-2-（3'，4'报道了-亚甲基二氧苯基）苯并呋喃11及其对金黄色葡萄球菌，枯草芽孢杆菌，白色念珠菌和大肠杆菌的抗菌活性。从麦草的种子中分离出原料烯醇5- [3''-（羟基）丙基] -7-甲氧基-2-（3'，4'亚甲基二氧苯基）苯并呋喃。这些化合物的结构解析（1-使用1D（（1）H，（13）C），2D NMR（HMBC，HMQC，COSY）和LCMS光谱数据建立11）。蛋黄酚和一些合成的新化合物对金黄色葡萄球菌，枯草芽孢杆菌，白色念珠菌和大肠杆菌显示相似的抗菌活性和MIC值，而其他新衍生物对金黄色葡萄球菌，枯草芽孢杆菌，C。显示出不同的活性。
• Benzofurans from <i>Styrax agrestis</i> As Acetylcholinesterase Inhibitors: Structure–Activity Relationships and Molecular Modeling Studies
  作者：Jiawei Liu、Vincent Dumontet、Anne-Laure Simonin、Bogdan I. Iorga、Vincent Guerineau、Marc Litaudon、Van Hung Nguyen、Françoise Gueritte

  DOI：10.1021/np200308j

  日期：2011.10.28

  An extract of Styrax agrestis fruits, collected in Vietnam, significantly inhibited acetylcholinesterase (AChE) in vitro. Bioassay-guided fractionation revealed three new egonol-type benzofurans: egonol-9(Z),12(Z) linoleate (1), 7-demethoxy-egonol-9(Z),12(Z) linoleate (2), and 7-demethoxyegonol oleate (4). Ten known egonol-type benzofurans were also isolated (3, 5, 6-13). In order to better understand structure activity relationships in this series, egonol derivatives 14-19 were prepared by chemical modifications and evaluated for their inhibition of AChE, butyrylcholinesterase (BChE), and AChE-induced A beta aggregation. Compounds 1-4 were the most potent inhibitors of the series, which exhibited inhibitory activity against AChE (IC50 1.4-3.1 mu M) and, for 1, A beta aggregation (77.6%). Molecular docking studies were also performed to investigate interaction of these compounds with the active site of AChE.