(S)-3,3-dimethyl-2-((S)-2-(methylamino)propanamido)-N-((S)-1-(4-(trifluoromethyl)phenethyl)piperidin-3-yl)butanamide | 1361322-74-8

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (S)-3,3-dimethyl-2-((S)-2-(methylamino)propanamido)-N-((S)-1-(4-(trifluoromethyl)phenethyl)piperidin-3-yl)butanamide
• 英文别名: (2S)-3,3-dimethyl-2-[[(2S)-2-(methylamino)propanoyl]amino]-N-[(3S)-1-[2-[4-(trifluoromethyl)phenyl]ethyl]piperidin-3-yl]butanamide
• CAS: 1361322-74-8
• 化学式: C₂₄H₃₇F₃N₄O₂
• 分子量: 470.579
• InChiKey: ALFIBOPSIAUNIQ-FFZOFVMBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.1
• 重原子数：
  33
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  73.5
• 氢给体数：
  3
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  (S)-3-Boc-氨基哌啶 在 盐酸 、 palladium 10% on activated carbon 、 甲酸铵 、 碳酸氢钠 、 1-羟基苯并三唑 、 O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate 、 三乙胺 、 N,N-二异丙基乙胺 、 sodium iodide 作用下， 以 1,4-二氧六环 、 甲醇 、 二氯甲烷 、 乙腈 为溶剂， 反应 5.33h， 生成 (S)-3,3-dimethyl-2-((S)-2-(methylamino)propanamido)-N-((S)-1-(4-(trifluoromethyl)phenethyl)piperidin-3-yl)butanamide
  参考文献：
  名称：

  Discovery of aminopiperidine-based Smac mimetics as IAP antagonists

  摘要：

  A series of structurally unique Smac mimetics that act as antagonists of inhibitor of apoptosis proteins (IAPs) has been discovered. While most previously described Smac mimetics contain the proline ring (or a similar cyclic motif) found in Smac, a key feature of the compounds described herein is that this ring has been removed. Despite this, compounds in this series potently bind to cIAP1 and elicit the expected phenotype of cIAP1 inhibition in cancer cells. Marked selectivity for cIAP1 over XIAP is observed for these compounds, which is attributed to a slight difference in the binding groove between the two proteins and the resulting steric interactions with the inhibitors. XIAP binding can be improved by constraining the inhibitor so that these unfavorable steric interactions are minimized. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2011.12.109