tert-butyl (3-(3-(2,5-dioxo-4-(pyridin-4-yl)-2,5-dihydro-1H-pyrrol-3-yl)-1H-indol-1-yl)propyl)carbamate | 1024584-23-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: tert-butyl (3-(3-(2,5-dioxo-4-(pyridin-4-yl)-2,5-dihydro-1H-pyrrol-3-yl)-1H-indol-1-yl)propyl)carbamate
• CAS: 1024584-23-3
• 化学式: C₂₅H₂₆N₄O₄
• 分子量: 446.506
• InChiKey: NVZXQFJPDGIXEZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.52
• 重原子数：
  33.0
• 可旋转键数：
  6.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  102.32
• 氢给体数：
  2.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  tert-butyl (3-(3-(2,5-dioxo-4-(pyridin-4-yl)-2,5-dihydro-1H-pyrrol-3-yl)-1H-indol-1-yl)propyl)carbamate 在 盐酸 作用下， 以 1,4-二氧六环 、 甲醇 为溶剂， 生成
  参考文献：
  名称：

  Aryl–indolyl maleimides as inhibitors of CaMKIIδ. Part 1: SAR of the aryl region

  摘要：

  A family of aryl-substituted maleimides was prepared and studied for their activity against calmodulin dependant kinase. Inhibitory activities against the enzyme ranged from 34 nM to > 20 mu M and were dependant upon both the nature of the aryl group and the hydrogen bond donating potential of the maleimide ring. Key interactions with the kinase ATP site and hinge region were found to be consistent with homology modeling predictions. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.02.059
• 作为产物：
  描述：

  4-吡啶乙酰胺 、 methyl 2-(1-(3-((tert-butoxycarbonyl)amino)propyl)-1H-indol-3-yl)-2-oxoacetate 在 potassium tert-butylate 作用下， 以 四氢呋喃 为溶剂， 生成 tert-butyl (3-(3-(2,5-dioxo-4-(pyridin-4-yl)-2,5-dihydro-1H-pyrrol-3-yl)-1H-indol-1-yl)propyl)carbamate
  参考文献：
  名称：

  Aryl–indolyl maleimides as inhibitors of CaMKIIδ. Part 1: SAR of the aryl region

  摘要：

  A family of aryl-substituted maleimides was prepared and studied for their activity against calmodulin dependant kinase. Inhibitory activities against the enzyme ranged from 34 nM to > 20 mu M and were dependant upon both the nature of the aryl group and the hydrogen bond donating potential of the maleimide ring. Key interactions with the kinase ATP site and hinge region were found to be consistent with homology modeling predictions. (C) 2008 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2008.02.059