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β-D-GlcpNAc-(1[*]2)-α-D-Manp | 47497-90-5

中文名称
——
中文别名
——
英文名称
β-D-GlcpNAc-(1[*]2)-α-D-Manp
英文别名
N-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(2S,3S,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxan-3-yl]acetamide
β-D-GlcpNAc-(1[*]2)-α-D-Manp化学式
CAS
47497-90-5
化学式
C14H25NO11
mdl
——
分子量
383.353
InChiKey
KGSIOYQZUFTKHO-QKSPDUFNSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -4.2
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    198
  • 氢给体数:
    8
  • 氢受体数:
    11

反应信息

  • 作为反应物:
    描述:
    乙酸酐β-D-GlcpNAc-(1[*]2)-α-D-Manp吡啶 为溶剂, 反应 12.0h, 以720 mg的产率得到2-O-(2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranosyl)-1,3,4,6-tetra-O-acetyl-α-D-mannopyranose
    参考文献:
    名称:
    Chemoenzymatic synthesis of the branched oligosaccharides which correspond to the core structures of N-linked sugar chains
    摘要:
    Synthetic routes are described to a partial structure common to all high mannose-type sugar chains and complex-type sugar chains based on a chemoenzymatic strategy which incorporates, (a) enzymatic synthesis of oligosaccharide blocks using glycosidases, and (b) chemical synthesis of the branching oligosaccharides via regioselective coupling. All reaction products correspond to key intermediates necessary for the construction of N-linked oligosaccharides and we have synthesized the branched tetra-manno-oligosaccharide high mannose-type sugar chain and the branched hexa-oligosaccharide complex-type sugar chain using this simple and direct method. (C) 1998 Elsevier Science Ltd.
    DOI:
    10.1016/s0008-6215(97)10001-5
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文献信息

  • Chemoenzymatic synthesis of the branched oligosaccharides which correspond to the core structures of N-linked sugar chains
    作者:Ichiro Matsuo、Megumi Isomura、Tatsuo Miyazaki、Tohru Sakakibara、Katsumi Ajisaka
    DOI:10.1016/s0008-6215(97)10001-5
    日期:1997.12
    Synthetic routes are described to a partial structure common to all high mannose-type sugar chains and complex-type sugar chains based on a chemoenzymatic strategy which incorporates, (a) enzymatic synthesis of oligosaccharide blocks using glycosidases, and (b) chemical synthesis of the branching oligosaccharides via regioselective coupling. All reaction products correspond to key intermediates necessary for the construction of N-linked oligosaccharides and we have synthesized the branched tetra-manno-oligosaccharide high mannose-type sugar chain and the branched hexa-oligosaccharide complex-type sugar chain using this simple and direct method. (C) 1998 Elsevier Science Ltd.
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