tert-butyl (2-(5-bromo-1H-indol-1-yl)ethyl)carbamate | 1443411-39-9

• 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: tert-butyl (2-(5-bromo-1H-indol-1-yl)ethyl)carbamate
• 英文别名: tert-butyl N-[2-(5-bromoindol-1-yl)ethyl]carbamate
• CAS: 1443411-39-9
• 化学式: C₁₅H₁₉BrN₂O₂
• 分子量: 339.232
• InChiKey: GEBNEASRJVLUTA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  43.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  tert-butyl (2-(5-bromo-1H-indol-1-yl)ethyl)carbamate 在 potassium tert-butylate 作用下， 以 乙醚 为溶剂， 反应 32.0h， 生成
  参考文献：
  名称：

  Characterization of Maleimide-Based Glycogen Synthase Kinase-3 (GSK-3) Inhibitors as Stimulators of Steroidogenesis

  摘要：

  Inhibition of GSK-3 beta has been well documented to account for the behavioral actions of the mood stabilizer lithium in various animal models of mood disorders. Recent studies have showed that genetic or pharmacological inhibition of GSK-3 beta resulted in anxiolytic-like and pro-social behavior. In our ongoing efforts to develop GSK-3 beta inhibitors for the treatment of mood disorders, SAR studies on maleimide-based compounds were undertaken. We present herein for the first time that some of these GSK-3 beta inhibitors, in particular analogues 1 and 9, were able to stimulate progesterone production in the MA-10 mouse tumor Leydig cell model of steroidogenesis without any significant toxicity. These two compounds were tested in the SmartCube behavioral assay and showed anxiolytic-like signatures following daily dose administration (50 mg/kg, ip) for 13 days. Taken together, these results support the hypothesis that GSK-3 beta inhibition could influence neuroactive steroid production thereby mediating the modulation of anxiety-like behavior in vivo.

  DOI：

  10.1021/jm400511s
• 作为产物：
  描述：

  5-溴吲哚 、 N-Boc-溴乙胺 在 potassium hydroxide 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以65 %的产率得到tert-butyl (2-(5-bromo-1H-indol-1-yl)ethyl)carbamate
  参考文献：
  名称：

  KR20220152761A

  摘要：

  公开号：

文献信息

• KR20220152761A
  申请人：——

  公开号：——

  公开（公告）日：——
• Characterization of Maleimide-Based Glycogen Synthase Kinase-3 (GSK-3) Inhibitors as Stimulators of Steroidogenesis
  作者：Hendra Gunosewoyo、Andrew Midzak、Irina N. Gaisina、Emily V. Sabath、Allison Fedolak、Taleen Hanania、Dani Brunner、Vassilios Papadopoulos、Alan P. Kozikowski

  DOI：10.1021/jm400511s

  日期：2013.6.27

  Inhibition of GSK-3 beta has been well documented to account for the behavioral actions of the mood stabilizer lithium in various animal models of mood disorders. Recent studies have showed that genetic or pharmacological inhibition of GSK-3 beta resulted in anxiolytic-like and pro-social behavior. In our ongoing efforts to develop GSK-3 beta inhibitors for the treatment of mood disorders, SAR studies on maleimide-based compounds were undertaken. We present herein for the first time that some of these GSK-3 beta inhibitors, in particular analogues 1 and 9, were able to stimulate progesterone production in the MA-10 mouse tumor Leydig cell model of steroidogenesis without any significant toxicity. These two compounds were tested in the SmartCube behavioral assay and showed anxiolytic-like signatures following daily dose administration (50 mg/kg, ip) for 13 days. Taken together, these results support the hypothesis that GSK-3 beta inhibition could influence neuroactive steroid production thereby mediating the modulation of anxiety-like behavior in vivo.