7,8,9,10,19,20,21,22-octahydrodinaphtho[2,3-b:2',3'-j][1,4,9,12]tetrathiacyclohexadecine-5,12,17,24-tetraone | 1404074-63-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 7,8,9,10,19,20,21,22-octahydrodinaphtho[2,3-b:2',3'-j][1,4,9,12]tetrathiacyclohexadecine-5,12,17,24-tetraone
• 英文别名: 7,8,9,10,19,20,21,22-Octahydrodinaphtho[2,3-b:2',3'-j][1,4,9,12]tetrathiacyclohexadecine-5,12,17,24-tetraone；2,7,18,23-tetrathiapentacyclo[22.8.0.08,17.010,15.026,31]dotriaconta-1(24),8(17),10,12,14,26,28,30-octaene-9,16,25,32-tetrone
• CAS: 1404074-63-0
• 化学式: C₂₈H₂₄O₄S₄
• 分子量: 552.76
• InChiKey: FMAPXZGGZANUTG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.8
• 重原子数：
  36
• 可旋转键数：
  0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  170
• 氢给体数：
  0
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  2,3-二氯-1,4-萘醌 、 1,4-丁二硫醇 在 三乙胺 作用下， 以 乙醇 为溶剂， 反应 8.0h， 以9%的产率得到7,8,9,10,19,20,21,22-octahydrodinaphtho[2,3-b:2',3'-j][1,4,9,12]tetrathiacyclohexadecine-5,12,17,24-tetraone
  参考文献：
  名称：

  Synthesis of novel 1,4-naphthoquinone derivatives: antibacterial and antifungal agents

  摘要：

  A novel series of substituted 1,4-naphthoquinone derivatives was synthesized and evaluated for antibacterial and antifungal activity. The structures of the novel products were characterized by spectroscopic methods. Among the tested compounds, 3a and 9 are the most effective compounds against M. luteum as potent antibacterial and C. tenuis and A. niger as potent antifungal. These two compounds are promising as biologically active compounds.

  DOI：

  10.1007/s00044-012-0300-y

文献信息

• Synthesis of novel 1,4-naphthoquinone derivatives: antibacterial and antifungal agents
  作者：Cemil Ibis、Amac Fatih Tuyun、Hakan Bahar、Sibel Sahinler Ayla、Maryna V. Stasevych、Rostyslav Ya. Musyanovych、Olena Komarovska-Porokhnyavets、Volodymyr Novikov

  DOI：10.1007/s00044-012-0300-y

  日期：2013.6

  A novel series of substituted 1,4-naphthoquinone derivatives was synthesized and evaluated for antibacterial and antifungal activity. The structures of the novel products were characterized by spectroscopic methods. Among the tested compounds, 3a and 9 are the most effective compounds against M. luteum as potent antibacterial and C. tenuis and A. niger as potent antifungal. These two compounds are promising as biologically active compounds.