tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbobenzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl) amino)-5-bis(carbobenzyloxy)guanidino-1-oxopentan-2-yl)carbamate | 1602523-33-0

• 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: tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbobenzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl) amino)-5-bis(carbobenzyloxy)guanidino-1-oxopentan-2-yl)carbamate
• CAS: 1602523-33-0
• 化学式: C₅₃H₆₅N₇O₁₄
• 分子量: 1024.14
• InChiKey: GCVDOADOWGCAOA-NZBNYWHUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.62
• 重原子数：
  74.0
• 可旋转键数：
  18.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  282.8
• 氢给体数：
  8.0
• 氢受体数：
  14.0

反应信息

• 作为反应物：
  描述：

  tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbobenzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl) amino)-5-bis(carbobenzyloxy)guanidino-1-oxopentan-2-yl)carbamate 在 1,4-环己二烯 、 palladium 10% on activated carbon 作用下， 以 溶剂黄146 为溶剂， 反应 14.0h， 生成
  参考文献：
  名称：

  Rigid spiroethers targeting the decoding center of the bacterial ribosome

  摘要：

  Continuing our efforts towards understanding the principles governing ribosomal recognition and function, we have synthesized and evaluated a series of diversely functionalized 5,6-, 6,6- and 7,6- spiroethers. These compounds successfully mimic natural aminoglycosides regarding their binding to the decoding center of the bacterial ribosome. Their potential to inhibit prokaryotic protein production in vitro along with their antibacterial potencies have also been examined. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2013.12.068
• 作为产物：
  描述：

  Boc-Arg(Cbz)₂-OH 、 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 N,N-二异丙基乙胺 作用下， 以 氘代四氢呋喃 为溶剂， 反应 12.0h， 以72%的产率得到tert-butyl ((S)-1-((((2S,5S,6R,7S,8R,10S)-6,7-dihydroxy-8,10-bis (carbobenzyloxyamino)-1-oxaspiro[4.5]decan-2-yl)methyl) amino)-5-bis(carbobenzyloxy)guanidino-1-oxopentan-2-yl)carbamate
  参考文献：
  名称：

  Rigid spiroethers targeting the decoding center of the bacterial ribosome

  摘要：

  Continuing our efforts towards understanding the principles governing ribosomal recognition and function, we have synthesized and evaluated a series of diversely functionalized 5,6-, 6,6- and 7,6- spiroethers. These compounds successfully mimic natural aminoglycosides regarding their binding to the decoding center of the bacterial ribosome. Their potential to inhibit prokaryotic protein production in vitro along with their antibacterial potencies have also been examined. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2013.12.068