2-(1-Hydroxy-6,8-dimethoxy-4-phenyl-2-naphthyl)-6,8-dimethoxy-4-phenyl-naphthalen-1-ol

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-(1-Hydroxy-6,8-dimethoxy-4-phenyl-2-naphthyl)-6,8-dimethoxy-4-phenyl-naphthalen-1-ol
• 英文别名: 2-(1-hydroxy-6,8-dimethoxy-4-phenylnaphthalen-2-yl)-6,8-dimethoxy-4-phenylnaphthalen-1-ol
• 化学式: C₃₆H₃₀O₆
• 分子量: 558.631
• InChiKey: PACXTSXSDCGLQG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.5
• 重原子数：
  42
• 可旋转键数：
  7
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.11
• 拓扑面积：
  77.4
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  1,4-Dihydroxy-5,7-dimethoxy-naphthalin 在 盐酸 、 4-二甲氨基吡啶 、 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 barium dihydroxide 、 硝酸 、 sodium acetate 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三乙胺 、 silver(l) oxide 、 锌 作用下， 以 甲醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 0.03h， 生成 2-(1-Hydroxy-6,8-dimethoxy-4-phenyl-2-naphthyl)-6,8-dimethoxy-4-phenyl-naphthalen-1-ol
  参考文献：
  名称：

  Structural analogues of the michellamine anti-HIV agents. Importance of the tetrahydroisoquinoline rings for biological activity

  摘要：

  A series of michellamine structural analogues was prepared in which the tetrahydroisoquinoline rings were substituted with a variety of simple aromatic ring systems. Additionally, the methyl groups on the central bis-naphthalene cores were replaced with hydrogen and methoxy. All the analogues were devoid of anti-HIV activity, suggesting that the heterocyclic portion of the tetrahydroisoquinoline ring is crucial for biological activity. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0960-894x(97)10057-9

文献信息

• Structural analogues of the michellamine anti-HIV agents. Importance of the tetrahydroisoquinoline rings for biological activity
  作者：Heping Zhang、David E Zembower、Zhidong Chen

  DOI：10.1016/s0960-894x(97)10057-9

  日期：1997.10

  A series of michellamine structural analogues was prepared in which the tetrahydroisoquinoline rings were substituted with a variety of simple aromatic ring systems. Additionally, the methyl groups on the central bis-naphthalene cores were replaced with hydrogen and methoxy. All the analogues were devoid of anti-HIV activity, suggesting that the heterocyclic portion of the tetrahydroisoquinoline ring is crucial for biological activity. (C) 1997 Elsevier Science Ltd.