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α-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranose | 3425-21-6

中文名称
——
中文别名
——
英文名称
α-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranose
英文别名
α-D-glucopyranosyl-(1->6)-cellobiose;beta-d-Glucopyranosyl-(1-6)-beta-d-glucopyranosyl-(1-4)-beta-d-glucopyranose;(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[(2R,3S,4R,5R,6R)-4,5,6-trihydroxy-2-(hydroxymethyl)oxan-3-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol
α-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranose化学式
CAS
3425-21-6
化学式
C18H32O16
mdl
——
分子量
504.442
InChiKey
OWEGMIWEEQEYGQ-MWMXWRIPSA-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):
    -6.9
  • 重原子数:
    34
  • 可旋转键数:
    7
  • 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

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:
    纤维素二糖蔗糖 在 Leuconostoc mesenteroides B-512 FMCM dextransucrase 作用下, 生成 α-D-glucopyranosyl-(1->2)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranose 、 α-D-glucopyranosyl-(1->2)-β-D-glucopyranosyl-(1->4)-α-D-glucopyranose 、 α-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl-(1->4)-β-D-glucopyranose 、 α-D-glucopyranosyl-(1->6)-β-D-glucopyranosyl-(1->4)-α-D-glucopyranose
    参考文献:
    名称:
    Potential Physiological Functions of Acceptor Products of Dextransucrase with Cellobiose as an Inhibitor of Mutansucrase and Fungal Cell Synthase
    摘要:
    A series of oligosaccharides (cellobio-oligosaccharides) ranging from degrees of polymer 3 to 6 were synthesized by Leuconostoc mesenteroides B-512 FMCM in the presence of cellobiose. The major oligosaccharides were the trisaccharides, alpha-D-glucopyranosyl-(1 -> 2)-beta-D-glucopyranosyl-(1-4)D-glucopyranose and alpha-D-glucopyranosyl-(1 -> 6)-[beta-D-glucopyranosyl-(1 -> 4)-D-glucopyranose. These cellobio-oligosaccharides were inhibitory on mutansucrase, an enzyme that causes dental caries. They were also found to be effective antifungal agents against Aspergillus terreus acting by inhibiting beta-(1 -> 3)-glucan synthase, which is required for fungal cell wall formation.
    DOI:
    10.1021/jf103140f
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文献信息

  • Potential Physiological Functions of Acceptor Products of Dextransucrase with Cellobiose as an Inhibitor of Mutansucrase and Fungal Cell Synthase
    作者:Misook Kim、Donal F. Day、Doman Kim
    DOI:10.1021/jf103140f
    日期:2010.11.10
    A series of oligosaccharides (cellobio-oligosaccharides) ranging from degrees of polymer 3 to 6 were synthesized by Leuconostoc mesenteroides B-512 FMCM in the presence of cellobiose. The major oligosaccharides were the trisaccharides, alpha-D-glucopyranosyl-(1 -> 2)-beta-D-glucopyranosyl-(1-4)D-glucopyranose and alpha-D-glucopyranosyl-(1 -> 6)-[beta-D-glucopyranosyl-(1 -> 4)-D-glucopyranose. These cellobio-oligosaccharides were inhibitory on mutansucrase, an enzyme that causes dental caries. They were also found to be effective antifungal agents against Aspergillus terreus acting by inhibiting beta-(1 -> 3)-glucan synthase, which is required for fungal cell wall formation.
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