6-benzyloxy-7-methoxy-1-[1-(4-benzyloxyphenyl)-2-(4-benzyloxy-5-methoxy-2-methoxymethoxyphenyl)-2-oxoethyl]isoquinoline | 422566-50-5

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: 6-benzyloxy-7-methoxy-1-[1-(4-benzyloxyphenyl)-2-(4-benzyloxy-5-methoxy-2-methoxymethoxyphenyl)-2-oxoethyl]isoquinoline
• 英文别名: 1-[5-Methoxy-2-(methoxymethoxy)-4-phenylmethoxyphenyl]-2-(7-methoxy-6-phenylmethoxyisoquinolin-1-yl)-2-(4-phenylmethoxyphenyl)ethanone
• CAS: 422566-50-5
• 化学式: C₄₈H₄₃NO₈
• 分子量: 761.871
• InChiKey: UEMHARNRJWFBDU-UHFFFAOYSA-N

物化性质

• 沸点：
  890.2±65.0 °C(predicted)
• 密度：
  1.225±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  9.4
• 重原子数：
  57
• 可旋转键数：
  18
• 环数：
  7.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  94.6
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  6-benzyloxy-7-methoxy-1-[1-(4-benzyloxyphenyl)-2-(4-benzyloxy-5-methoxy-2-methoxymethoxyphenyl)-2-oxoethyl]isoquinoline 在 盐酸 作用下， 以 甲醇 为溶剂， 反应 22.5h， 生成 Ethyl 2-[1-[2-(2-hydroxy-5-methoxy-4-phenylmethoxyphenyl)-2-oxo-1-(4-phenylmethoxyphenyl)ethyl]-7-methoxy-6-phenylmethoxyisoquinolin-2-ium-2-yl]acetate;bromide
  参考文献：
  名称：

  Synthesis and Structure−Activity Relationship Study of Lamellarin Derivatives

  摘要：

  Ten derivatives (3-12) of marine alkaloid lamellarin D (1) were synthesized and evaluated for cytotoxicity against a HeLa cell line in an effort to examine their structure-activity relationships. It appeared that the hydroxyl groups at positions C-8 and C-20 of 1 were important structural requirements for cytotoxic activity, while the hydroxyl group at C-14 and the two methoxy groups at C-13 and C-21 were not necessary for the activity.

  DOI：

  10.1021/np0104525
• 作为产物：
  描述：

  methyl 4-benzyloxy-5-methoxy-2-hydroxybenzoate 在 sodium hydride 、 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 2.0h， 生成 6-benzyloxy-7-methoxy-1-[1-(4-benzyloxyphenyl)-2-(4-benzyloxy-5-methoxy-2-methoxymethoxyphenyl)-2-oxoethyl]isoquinoline
  参考文献：
  名称：

  Synthesis and Structure−Activity Relationship Study of Lamellarin Derivatives

  摘要：

  Ten derivatives (3-12) of marine alkaloid lamellarin D (1) were synthesized and evaluated for cytotoxicity against a HeLa cell line in an effort to examine their structure-activity relationships. It appeared that the hydroxyl groups at positions C-8 and C-20 of 1 were important structural requirements for cytotoxic activity, while the hydroxyl group at C-14 and the two methoxy groups at C-13 and C-21 were not necessary for the activity.

  DOI：

  10.1021/np0104525