N-cyclohexyl-N-(6-oxohexyl)acetamide | 1428247-69-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: N-cyclohexyl-N-(6-oxohexyl)acetamide
• CAS: 1428247-69-1
• 化学式: C₁₄H₂₅NO₂
• 分子量: 239.358
• InChiKey: QZASEYNVIZQZFX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  17
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  37.4
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-脱氧野尻霉素 、 N-cyclohexyl-N-(6-oxohexyl)acetamide 在 palladium on activated charcoal 、 溶剂黄146 作用下， 以 乙醇 为溶剂， 生成 N-cyclohexyl-N-(6-((2R,3R,4R,5S)-3,4,5-trihydroxy-2-(hydroxymethyl) piperidin-1-yl)hexyl)acetamide
  参考文献：
  名称：

  N-Alkyldeoxynojirimycin derivatives with novel terminal tertiary amide substitution for treatment of bovine viral diarrhea virus (BVDV), Dengue, and Tacaribe virus infections

  摘要：

  Novel N-alkyldeoxynojirimycins (NADNJs) with two hydrophobic groups attached to a nitrogen linker on the alkyl chain were designed. A novel NADNJ containing a terminal tertiary carboxamide moiety was discovered that was a potent inhibitor against BVDV. Further optimization resulted in a structurally more stable lead compound 24 with a submicromolar EC50 against BVDV, Dengue, and Tacaribe; and low cytotoxicity. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.01.108

文献信息

• N-Alkyldeoxynojirimycin derivatives with novel terminal tertiary amide substitution for treatment of bovine viral diarrhea virus (BVDV), Dengue, and Tacaribe virus infections
  作者：Yanming Du、Hong Ye、Tina Gill、Lijuan Wang、Fang Guo、Andrea Cuconati、Ju-Tao Guo、Timothy M. Block、Jinhong Chang、Xiaodong Xu

  DOI：10.1016/j.bmcl.2013.01.108

  日期：2013.4

  Novel N-alkyldeoxynojirimycins (NADNJs) with two hydrophobic groups attached to a nitrogen linker on the alkyl chain were designed. A novel NADNJ containing a terminal tertiary carboxamide moiety was discovered that was a potent inhibitor against BVDV. Further optimization resulted in a structurally more stable lead compound 24 with a submicromolar EC50 against BVDV, Dengue, and Tacaribe; and low cytotoxicity. (C) 2013 Elsevier Ltd. All rights reserved.