O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-6)-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1-4)-O-(3,6-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranosyl)-(1-6)-1,2,3,4,5-penta-O-acetyl-D-myo-inositol | 123487-63-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-6)-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1-4)-O-(3,6-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranosyl)-(1-6)-1,2,3,4,5-penta-O-acetyl-D-myo-inositol
• CAS: 123487-63-8
• 化学式: C₉₈H₁₀₇NO₂₇
• 分子量: 1730.92
• InChiKey: HUYDTRGLTHQERY-MQMAZPAESA-N

计算性质

• 辛醇/水分配系数(LogP)：
  12.22
• 重原子数：
  126.0
• 可旋转键数：
  41.0
• 环数：
  13.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  319.28
• 氢给体数：
  2.0
• 氢受体数：
  27.0

反应信息

• 作为反应物：
  描述：

  O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-6)-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1-4)-O-(3,6-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranosyl)-(1-6)-1,2,3,4,5-penta-O-acetyl-D-myo-inositol 、 3,4,6-tri-O-benzoyl-β-D-mannopyranose 1,2-(pent-4-enyl orthobenzoate) 在 N-碘代丁二酰亚胺 、 三氟甲磺酸 作用下， 生成 O-(2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl)-(1-2)-O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-6)-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1-4)-O-(3,6-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranosyl)-(1-6)-1,2,3,4,5-pent
  参考文献：
  名称：

  Studies Related to Synthesis of Glycophosphatidylinositol Membrane-Bound Protein Anchors. 6. Convergent Assembly of Subunits

  摘要：

  Glycophosphatidylinositol anchors of membrane-bound proteins are thought to comprise a common pentasaccharide core containing mannan, glucosamine, and inositol residues. A synthetic route to this core is described. In addition, the complete heptasaccharide moiety of the rat brain Thy-1 membrane anchor, the first mammalian membrane anchor to be characterized, has been synthesized. In the case of the Thy-1 anchor, the synthetic plan is based on three building blocks comprising glucosamine-inositol, galactosamine-mannose, and trimannan residues. Although glycosyl donors other than n-pentenyl glycosides (NPGs) have been used in preparing each of these building blocks, the final assembly of the heptasaccharide utilizes NPGs as the only glycosyl donors. The mildness of the conditions for these coupling reactions has allowed us to make provisions for subsequent installation of the three phosphodiester units.

  DOI：

  10.1021/ja00110a011
• 作为产物：
  描述：

  在 硫脲 作用下， 以 乙醇 为溶剂， 反应 1.0h， 生成 O-(3,4,6-tri-O-benzyl-α-D-mannopyranosyl)-(1-6)-O-(2,3,4-tri-O-benzyl-α-D-mannopyranosyl)-(1-4)-O-(3,6-di-O-benzyl-2-<(benzyloxycarbonyl)amino>-2-deoxy-α-D-glucopyranosyl)-(1-6)-1,2,3,4,5-penta-O-acetyl-D-myo-inositol
  参考文献：
  名称：

  Studies Related to Synthesis of Glycophosphatidylinositol Membrane-Bound Protein Anchors. 6. Convergent Assembly of Subunits

  摘要：

  Glycophosphatidylinositol anchors of membrane-bound proteins are thought to comprise a common pentasaccharide core containing mannan, glucosamine, and inositol residues. A synthetic route to this core is described. In addition, the complete heptasaccharide moiety of the rat brain Thy-1 membrane anchor, the first mammalian membrane anchor to be characterized, has been synthesized. In the case of the Thy-1 anchor, the synthetic plan is based on three building blocks comprising glucosamine-inositol, galactosamine-mannose, and trimannan residues. Although glycosyl donors other than n-pentenyl glycosides (NPGs) have been used in preparing each of these building blocks, the final assembly of the heptasaccharide utilizes NPGs as the only glycosyl donors. The mildness of the conditions for these coupling reactions has allowed us to make provisions for subsequent installation of the three phosphodiester units.

  DOI：

  10.1021/ja00110a011

文献信息

• n-Pentenyl glycosides facilitate a stereoselective synthesis of the pentasaccharide core of the protein membrane anchor found in Trypanosoma brucei
  作者：David R. Mootoo、Peter Konradsson、Bert Fraser-Reid

  DOI：10.1021/ja00204a049

  日期：1989.10