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4-O-β-D-glucopyranosyl-D-glucosamine

中文名称
——
中文别名
——
英文名称
4-O-β-D-glucopyranosyl-D-glucosamine
英文别名
Glc(b1-4)GlcN;(2S,3R,4S,5S,6R)-2-[(2R,3S,4R,5R)-5-amino-4,6-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
4-O-β-D-glucopyranosyl-D-glucosamine化学式
CAS
——
化学式
C12H23NO10
mdl
——
分子量
341.315
InChiKey
PNIWLNAGKUGXDO-LMXLUCEESA-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):
    -5
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    195
  • 氢给体数:
    8
  • 氢受体数:
    11

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-deoxy-2-amino glucose对氟苯甲醇 在 Tris-HCl buffer 、 magnesium chloride 作用下, 以 乙醇丙酮 为溶剂, 反应 24.0h, 以55%的产率得到4-O-β-D-glucopyranosyl-D-glucosamine
    参考文献:
    名称:
    Synthesis and structural analysis of disaccharides of 4-O-β-d-glucopyranosyl-d-glucosamine and 4-O-d-β-glucopyranosyl-2-deoxy-d-glucose
    摘要:
    The disaccharides 4-O-beta-D-glucopyranosyl-D-glucosamine (Glc-GlcN) and 4-O-beta-D-glucopyranosyl-2-deoxy-D-glucose (Glc-2-deoxy-Glc) were synthesized from equimolar amounts of D-glucosamine and alpha-D-glucose-1-phosphate (G-1-P), and 2-deoxy-D-glucose and alpha-D-glucose-1-phosphate (G-1-P) respectively, in the presence of cellobiose phosphorylase from Cellvibrio gilvus. The yields were 55% and 50% based on the initial amounts of D-glucosamine and 2-deoxy-D-glucose, respectively. The structure of disaccharides were confirmed by NMR analysis.
    DOI:
    10.1016/0008-6215(95)00143-h
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文献信息

  • Synthesis and structural analysis of disaccharides of 4-O-β-d-glucopyranosyl-d-glucosamine and 4-O-d-β-glucopyranosyl-2-deoxy-d-glucose
    作者:M.A. Tariq、K. Hayashi、K. Tokuyasu、T. Nagata
    DOI:10.1016/0008-6215(95)00143-h
    日期:1995.9
    The disaccharides 4-O-beta-D-glucopyranosyl-D-glucosamine (Glc-GlcN) and 4-O-beta-D-glucopyranosyl-2-deoxy-D-glucose (Glc-2-deoxy-Glc) were synthesized from equimolar amounts of D-glucosamine and alpha-D-glucose-1-phosphate (G-1-P), and 2-deoxy-D-glucose and alpha-D-glucose-1-phosphate (G-1-P) respectively, in the presence of cellobiose phosphorylase from Cellvibrio gilvus. The yields were 55% and 50% based on the initial amounts of D-glucosamine and 2-deoxy-D-glucose, respectively. The structure of disaccharides were confirmed by NMR analysis.
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