(S)-4-(tert-butoxy)-5-methyl-1-((S)-1-((S)-2-methyl-1-((S)-1-((S)-2-methyl-5-oxo-2,5-dihydro-1H-pyrrol-3-yl)pyrrolidin-3-yl)-5-oxo-2,5-dihydro-1H-pyrrol-3-yl)pyrrolidin-3-yl)-1H-pyrrol-2(5H)-one | 1316848-32-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯啉
• 英文名称: (S)-4-(tert-butoxy)-5-methyl-1-((S)-1-((S)-2-methyl-1-((S)-1-((S)-2-methyl-5-oxo-2,5-dihydro-1H-pyrrol-3-yl)pyrrolidin-3-yl)-5-oxo-2,5-dihydro-1H-pyrrol-3-yl)pyrrolidin-3-yl)-1H-pyrrol-2(5H)-one
• 英文别名: (2S)-2-methyl-3-[(3S)-3-[(2S)-2-methyl-3-[(2-methylpropan-2-yl)oxy]-5-oxo-2H-pyrrol-1-yl]pyrrolidin-1-yl]-1-[(3S)-1-[(2S)-2-methyl-5-oxo-1,2-dihydropyrrol-3-yl]pyrrolidin-3-yl]-2H-pyrrol-5-one
• CAS: 1316848-32-4
• 化学式: C₂₇H₃₉N₅O₄
• 分子量: 497.638
• InChiKey: MOJBJKOBSVCHBO-HVTWWXFQSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.8
• 重原子数：
  36
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  85.4
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  (S)-5-methylpyrrolidine-2,4-dione 在 三氟乙酸 、 原甲酸三甲酯 作用下， 以 二氯甲烷 、 异丙醇 为溶剂， 反应 22.0h， 生成 (S)-4-(tert-butoxy)-5-methyl-1-((S)-1-((S)-2-methyl-1-((S)-1-((S)-2-methyl-5-oxo-2,5-dihydro-1H-pyrrol-3-yl)pyrrolidin-3-yl)-5-oxo-2,5-dihydro-1H-pyrrol-3-yl)pyrrolidin-3-yl)-1H-pyrrol-2(5H)-one
  参考文献：
  名称：

  Pyrrolinone–Pyrrolidine Oligomers as Universal Peptidomimetics

  摘要：

  Peptidomimetics 1-3 were prepared from amino acid-derived tetramic acids 7 as the key starting materials. Calculations show that preferred conformations of 1 can align their side-chain vectors with amino acids in common secondary structures more effectively than conformations of 3. A good fit was found for a preferred conformation of 2 (an extended derivative of 1) with a sheet/beta-turn/sheet motif.

  DOI：

  10.1021/ja2033734

文献信息

• PEPTIDOMIMETIC COMPOUNDS AND RELATED METHODS
  申请人：Burgess Kevin

  公开号：US20130288331A1

  公开（公告）日：2013-10-31

  Provided herein are compounds and methods of using same for the perturbation and/or inhibition of protein-protein interactions. Also provided herein is a data mining method useful for the identification of protein-protein interactions that may be inhibited by these compounds.