benzyl 2-(6-chloro-9-(3-nitrobenzyl)-9H-carbazol-2-yl)propanoate | 918547-61-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: benzyl 2-(6-chloro-9-(3-nitrobenzyl)-9H-carbazol-2-yl)propanoate
• 英文别名: Benzyl 2-[6-chloro-9-[(3-nitrophenyl)methyl]carbazol-2-yl]propanoate
• CAS: 918547-61-2
• 化学式: C₂₉H₂₃ClN₂O₄
• 分子量: 498.966
• InChiKey: ZJXALESNEUFTSV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.2
• 重原子数：
  36
• 可旋转键数：
  7
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.14
• 拓扑面积：
  77
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  benzyl 2-(6-chloro-9-(3-nitrobenzyl)-9H-carbazol-2-yl)propanoate 在 乙醇 、 tin(ll) chloride 作用下， 反应 3.0h， 生成 benzyl 2-(9-(3-aminobenzyl)-3-chloro-9H-carbazol-7-yl)propanoate
  参考文献：
  名称：

  Scaffold of the Cyclooxygenase-2 (COX-2) Inhibitor Carprofen Provides Alzheimer γ-Secretase Modulators

  摘要：

  N-Sulfonylated and N-alkylated carprofen derivatives were investigated for their inhibition and modulation of gamma-secretase, which is associated with Alzheimer's disease. The introduction of a lipophilic substituent transformed the COX-2 inhibitor carprofen into a potent gamma-secretase modulator. Several compounds (e.g., 9p, 11f) caused selective reduction of A beta(42) and an increase of A beta(38). The most active compounds displayed activities in the low micromolar range and no effect on the gamma-secretase cleavage at the epsilon-site.

  DOI：

  10.1021/jm0610200
• 作为产物：
  描述：

  卡洛芬 在 sodium hydride 、 potassium carbonate 作用下， 以 四氢呋喃 、 N,N-二甲基甲酰胺 为溶剂， 反应 3.0h， 生成 benzyl 2-(6-chloro-9-(3-nitrobenzyl)-9H-carbazol-2-yl)propanoate
  参考文献：
  名称：

  Scaffold of the Cyclooxygenase-2 (COX-2) Inhibitor Carprofen Provides Alzheimer γ-Secretase Modulators

  摘要：

  N-Sulfonylated and N-alkylated carprofen derivatives were investigated for their inhibition and modulation of gamma-secretase, which is associated with Alzheimer's disease. The introduction of a lipophilic substituent transformed the COX-2 inhibitor carprofen into a potent gamma-secretase modulator. Several compounds (e.g., 9p, 11f) caused selective reduction of A beta(42) and an increase of A beta(38). The most active compounds displayed activities in the low micromolar range and no effect on the gamma-secretase cleavage at the epsilon-site.

  DOI：

  10.1021/jm0610200