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(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-((2S,3S,4S,5R)-3,4-Dihydroxy-2,5-bis-hydroxymethyl-tetrahydro-furan-2-yloxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yloxy]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol

中文名称
——
中文别名
——
英文名称
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-((2S,3S,4S,5R)-3,4-Dihydroxy-2,5-bis-hydroxymethyl-tetrahydro-furan-2-yloxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yloxy]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol
英文别名
Glc(b1-2)Glc(a1-2b)Fruf;(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-((2S,3S,4S,5R)-3,4-Dihydroxy-2,5-bis-hydroxymethyl-tetrahydro-furan-2-yloxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yloxy]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol化学式
CAS
——
化学式
C18H32O16
mdl
——
分子量
504.442
InChiKey
LNRUEZIDUKQGRH-HRUWSWHBSA-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):
    -5.3
  • 重原子数:
    34
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    269
  • 氢给体数:
    11
  • 氢受体数:
    16

反应信息

  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 sodium tetrahydroborate 作用下, 以 为溶剂, 生成 O-α-D-glucopyranosyl-(1â 4)-β-D-glucopyranosyl α-D-glucopyranoside 、 α-glucosyl-sucrose 、 (2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-((2S,3S,4S,5R)-3,4-Dihydroxy-2,5-bis-hydroxymethyl-tetrahydro-furan-2-yloxy)-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-3-yloxy]-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 、 O-α-D-glucopyranosyl-(1â 4)-α-D-glucopyranosyl β-D-glucopyranoside
    参考文献:
    名称:
    Structural determination of some new oligosaccharides and analysis of the branching pattern of isomaltooligosaccharides from beer
    摘要:
    Separation of the low molecular weight fraction of oligosaccharides from beer and subsequent NMR analysis led to the identification of several new derivatives of trehalose, sucrose, maltooligosaccharides glucosylated at O-2 of reducing end Glc, and linear Glc oligomers with alpha-(1-->3) and alpha-(1-->4)-linkages. Reducing oligosaccharides were labeled with 7-amino-4-methylcoumarin by reductive amination, separated according to their molecular weight and the branching pattern was studied using enzymatic (pullulanase) degradation in combination with MALDI-TOF mass spectrometry and HPLC analysis. It was found that up to DP 10 isomaltooligosaccharides mostly consisted of a linear reducing alpha-(1-->4)-linked Glc chain substituted by single maltose or maltotriose residue at O-6 of any residue except the reducing one. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(98)00119-0
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