tert-butyl (3-aminopropyl)((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)carbamate | 1092578-55-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 类固醇和类固醇衍生物
• 英文名称: tert-butyl (3-aminopropyl)((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)carbamate
• CAS: 1092578-55-6
• 化学式: C₃₅H₆₂N₂O₂
• 分子量: 542.889
• InChiKey: COUOLNMNVMALIA-FWJKXKDPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.98
• 重原子数：
  39.0
• 可旋转键数：
  9.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  55.56
• 氢给体数：
  1.0
• 氢受体数：
  3.0

反应信息

• 作为反应物：
  描述：

  tert-butyl (3-aminopropyl)((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)carbamate 在 哌啶 、 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 25.5h， 生成 tert-butyl (15S)-5-[3β-cholest-5-en-3-yl]-15-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-2,2-dimethyl-4,10,14-trioxo-3-oxa-5,9,13-triazaoctadecan-18-oate
  参考文献：
  名称：

  Fluorescent mimics of cholesterol that rapidly bind surfaces of living mammalian cells

  摘要：

  新型类固醇类似物通过受体介导的途径迅速大量地被纳入活体哺乳动物细胞的质膜中。

  DOI：

  10.1039/c5cc06325f
• 作为产物：
  描述：

  tert-butyl-3β-cholest-5-en-3-yl[3-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)propyl]carbamate 在 肼 作用下， 以 乙醇 为溶剂， 反应 4.0h， 以99%的产率得到tert-butyl (3-aminopropyl)((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)carbamate
  参考文献：
  名称：

  Fluorescent mimics of cholesterol that rapidly bind surfaces of living mammalian cells

  摘要：

  新型类固醇类似物通过受体介导的途径迅速大量地被纳入活体哺乳动物细胞的质膜中。

  DOI：

  10.1039/c5cc06325f

文献信息

• Selective Disruption of Early/Recycling Endosomes: Release of Disulfide-Linked Cargo Mediated by a <i>N</i>-Alkyl-3β-Cholesterylamine-Capped Peptide
  作者：Qi Sun、Sutang Cai、Blake R. Peterson

  DOI：10.1021/ja803380a

  日期：2008.8.1

  The use of endocytic uptake pathways to deliver poorly permeable molecules into mammalian cells is often plagued by entrapment and degradation of material in late endosomes and lysosomes. As a strategy to prevent the exposure of cargo to these highly hydrolytic membrane-sealed compartments, we synthesized derivatives of the membrane anchor N-alkyl-3 beta-cholesterylamine that selectively target linked compounds to less hydrolytic early/recycling endosomes. By targeting a pH-dependent membrane-lytic dodecapeptide and dislufide-linked flurophore to these compartments in Chinese hamster ovary cells or Jurkat lymphocytes, membranes of early-recycling endosomes were selectively disrupted, resulting in cleavage of the disulphide and escape of the fluorophore into cytosol and nucleus with low toxicity. The ability os appropriately designed N-alkyl-3 beta-cholesterylamines to deliver cargo into and release dislufide-linked cargo from relatively nonhydrolytic early/recycling endosomes may be useful for the delivery of a variety of sensitive molecules into living mammalian cells.
• [EN] SYNTHETIC CHOLESTERYLAMINE-LINKER DERIVATIVES FOR AGENT DELIVERY INTO CELLS<br/>[FR] DÉRIVÉS SYNTHÉTIQUES DE CHOLESTÉRYLAMINE-LIEUR POUR L'ADMINISTRATION INTRACELLULAIRE D'AGENTS
  申请人：UNIV KANSAS

  公开号：WO2011019942A3

  公开（公告）日：2011-07-14