3-(benzyloxycarbonylamino)propyl 3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranoside | 1308292-88-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3-(benzyloxycarbonylamino)propyl 3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
• CAS: 1308292-88-7
• 化学式: C₁₂₃H₉₉N₅O₃₅
• 分子量: 2207.15
• InChiKey: UXHNWKFUDLNIEX-OKPRKQOASA-N

计算性质

• 辛醇/水分配系数(LogP)：
  12.73
• 重原子数：
  163.0
• 可旋转键数：
  37.0
• 环数：
  21.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  492.32
• 氢给体数：
  2.0
• 氢受体数：
  35.0

反应信息

• 作为反应物：
  描述：

  ethyl 2-acetamido-6-O-acetyl-3,4-di-O-benzoyl-2-deoxy-β-D-glucopyranosyl-(1-> 6)-3,4-di O-benzoyl-2-deoxy-2-phthalimido-1-thio-β-D-glucopyranoside 、 3-(benzyloxycarbonylamino)propyl 3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranoside 在 N-碘代丁二酰亚胺 、 三氟甲磺酸 作用下， 以 二氯甲烷 为溶剂， 反应 0.5h， 生成
  参考文献：
  名称：

  Synthesis of five nona-β-(1→6)-d-glucosamines with various patterns of N-acetylation corresponding to the fragments of exopolysaccharide of Staphylococcus aureus

  摘要：

  A series of five 3-acetamidopropyl beta-glycosides of nona-beta-(1 -> 6)-glucosamines containing two N-acetyl-glucosamine residues separated by a different number of glucosamine units with free amino groups have been synthesized using a convergent blockwise approach. Oxazoline glycosylation was used to introduce N-acetylglucosamine residues. These nonasaccharides are structurally related to the poly-N-acetylglucosamine (PNAG) extracellular polysaccharide of Staphylococcus aureus and can be used as models for biochemical and immunological studies. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2011.02.018
• 作为产物：
  描述：

  在 甲醇 、 乙酰氯 作用下， 以 二氯甲烷 为溶剂， 反应 16.0h， 生成 3-(benzyloxycarbonylamino)propyl 3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl-(1-> 6)-3,4-di-O-benzoyl-2-deoxy-2-phthalimido-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of five nona-β-(1→6)-d-glucosamines with various patterns of N-acetylation corresponding to the fragments of exopolysaccharide of Staphylococcus aureus

  摘要：

  A series of five 3-acetamidopropyl beta-glycosides of nona-beta-(1 -> 6)-glucosamines containing two N-acetyl-glucosamine residues separated by a different number of glucosamine units with free amino groups have been synthesized using a convergent blockwise approach. Oxazoline glycosylation was used to introduce N-acetylglucosamine residues. These nonasaccharides are structurally related to the poly-N-acetylglucosamine (PNAG) extracellular polysaccharide of Staphylococcus aureus and can be used as models for biochemical and immunological studies. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.carres.2011.02.018