ethyl 3-(2-naphthoyl)-7-benzoylindolizine-1-carboxylate | 374679-27-3

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: ethyl 3-(2-naphthoyl)-7-benzoylindolizine-1-carboxylate
• 英文别名: Ethyl 7-benzoyl-3-(naphthalene-2-carbonyl)indolizine-1-carboxylate
• CAS: 374679-27-3
• 化学式: C₂₉H₂₁NO₄
• 分子量: 447.49
• InChiKey: OMNFLCJXENKOCL-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7
• 重原子数：
  34
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  64.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  ethyl 3-(2-naphthoyl)-7-benzoylindolizine-1-carboxylate 在 sodium hydroxide 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 5.0h， 生成 3-(2-naphthoyl)-7-benzoylindolizine-1-carboxylic acid
  参考文献：
  名称：

  Indolizine Derivatives as HIV-1 VIF-ElonginC Interaction Inhibitors

  摘要：

  Compound 1 (VEC‐5) was identified as a potent small‐molecular HIV‐1 viron infectivity factor inhibitor that targets the viron infectivity factor–ElonginC interaction. A structure–activity relationship study was carried out to develop compounds with improved efficacy against HIV‐1 and 49 indolizine derivatives of three categories were designed and synthesized. We found that five compounds exhibited promising anti‐HIV‐1 activity, and the most active compound 2g had an IC50 value of 11.0 μm. These results provide new information to develop highly potent small‐molecule HIV‐1 viron infectivity factor inhibitors.

  DOI：

  10.1111/cbdd.12119
• 作为产物：
  描述：

  4-苯甲酰吡啶 在 potassium carbonate 作用下， 以 乙酸乙酯 、 乙腈 为溶剂， 反应 72.5h， 生成 ethyl 3-(2-naphthoyl)-7-benzoylindolizine-1-carboxylate
  参考文献：
  名称：

  Indolizine Derivatives as HIV-1 VIF-ElonginC Interaction Inhibitors

  摘要：

  Compound 1 (VEC‐5) was identified as a potent small‐molecular HIV‐1 viron infectivity factor inhibitor that targets the viron infectivity factor–ElonginC interaction. A structure–activity relationship study was carried out to develop compounds with improved efficacy against HIV‐1 and 49 indolizine derivatives of three categories were designed and synthesized. We found that five compounds exhibited promising anti‐HIV‐1 activity, and the most active compound 2g had an IC50 value of 11.0 μm. These results provide new information to develop highly potent small‐molecule HIV‐1 viron infectivity factor inhibitors.

  DOI：

  10.1111/cbdd.12119

文献信息

• Indolizine Derivatives as HIV-1 VIF-ElonginC Interaction Inhibitors
  作者：Wenlin Huang、Tao Zuo、Xiao Luo、Hongwei Jin、Zhenming Liu、Zhenjun Yang、Xianghui Yu、Liangren Zhang、Lihe Zhang

  DOI：10.1111/cbdd.12119

  日期：2013.6

  Compound 1 (VEC‐5) was identified as a potent small‐molecular HIV‐1 viron infectivity factor inhibitor that targets the viron infectivity factor–ElonginC interaction. A structure–activity relationship study was carried out to develop compounds with improved efficacy against HIV‐1 and 49 indolizine derivatives of three categories were designed and synthesized. We found that five compounds exhibited promising anti‐HIV‐1 activity, and the most active compound 2g had an IC50 value of 11.0 μm. These results provide new information to develop highly potent small‐molecule HIV‐1 viron infectivity factor inhibitors.