N-[5-(methylsulfanyl)pentyl]-2-quinolinecarboxamide | 1350981-66-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: N-[5-(methylsulfanyl)pentyl]-2-quinolinecarboxamide
• 英文别名: N-(5-methylsulfanylpentyl)quinoline-2-carboxamide
• CAS: 1350981-66-6
• 化学式: C₁₆H₂₀N₂OS
• 分子量: 288.414
• InChiKey: BNASDRLLOURYJB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  20
• 可旋转键数：
  7
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  67.3
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-[5-(methylsulfanyl)pentyl]-2-quinolinecarboxamide 在 Oxone 作用下， 以 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 以44%的产率得到N-[5-(methylsulfonyl)pentyl]-2-quinolinecarboxamide
  参考文献：
  名称：

  Synthesis of 2-quinolinecarboxamide derivatives as potential HDAC inhibitors

  摘要：

  Inhibition of histone deacetylase activity appears as an original and effective approach for the treatment of cancer. A series of novel quinoline-containing derivatives has been synthesized and found that some of these compounds possess nanomolar histone deacetylase inhibitory activity.

  DOI：

  10.1007/s10593-011-0825-x
• 作为产物：
  描述：

  喹哪啶酸 在 四溴化碳 、 三苯基膦 、 N,N'-羰基二咪唑 作用下， 以 四氢呋喃 、 乙醇 、 水 、 乙腈 为溶剂， 反应 40.0h， 生成 N-[5-(methylsulfanyl)pentyl]-2-quinolinecarboxamide
  参考文献：
  名称：

  Synthesis of 2-quinolinecarboxamide derivatives as potential HDAC inhibitors

  摘要：

  Inhibition of histone deacetylase activity appears as an original and effective approach for the treatment of cancer. A series of novel quinoline-containing derivatives has been synthesized and found that some of these compounds possess nanomolar histone deacetylase inhibitory activity.

  DOI：

  10.1007/s10593-011-0825-x

文献信息

• Synthesis of 2-quinolinecarboxamide derivatives as potential HDAC inhibitors
  作者：O. Habarova、O. Bobiļeva、E. Loža、N. Romančikova

  DOI：10.1007/s10593-011-0825-x

  日期：2011.9

  Inhibition of histone deacetylase activity appears as an original and effective approach for the treatment of cancer. A series of novel quinoline-containing derivatives has been synthesized and found that some of these compounds possess nanomolar histone deacetylase inhibitory activity.