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2-deoxy-β-D-arabino-hexopyranosyl-(1->4)-2-deoxy-D-arabino-hexose

中文名称
——
中文别名
——
英文名称
2-deoxy-β-D-arabino-hexopyranosyl-(1->4)-2-deoxy-D-arabino-hexose
英文别名
2-deoxy-D-araHex(b1-4)2-deoxy-D-araHex;(4R,5S,6R)-5-[(2S,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,4-diol
2-deoxy-β-D-arabino-hexopyranosyl-(1->4)-2-deoxy-D-arabino-hexose化学式
CAS
——
化学式
C12H22O9
mdl
——
分子量
310.301
InChiKey
IKIMNPXVMZDSPX-OQEOTTNJSA-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):
    -2.8
  • 重原子数:
    21
  • 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:
    149
  • 氢给体数:
    6
  • 氢受体数:
    9

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-D-glucoseD-葡萄烯糖 在 cellobiose phosphorylase from Cellvibrio gilvus 、 MOPS buffer 作用下, 以 为溶剂, 反应 170.0h, 以59%的产率得到2-deoxy-β-D-arabino-hexopyranosyl-(1->4)-2-deoxy-D-arabino-hexose
    参考文献:
    名称:
    Reaction on d-glucal by an inverting phosphorylase to synthesize derivatives of 2-deoxy-β-d-arabino-hexopyranosyl-(1→4)-d-glucose (2II-deoxycellobiose)
    摘要:
    Four derivatives of 2(11)-deoxycellobiose were synthesized from D-glucal and acceptor sugars (D-glucose, D-xylose, D-mannose, and 2-deoxy-D-arabino-hexose) using a cellobiose phosphorylase from Cellvibrio gilvus. The enzyme was found to be an effective catalyst to synthesize the beta-(1 -> 4) linkage of 2-dcoxy-D-arabhio-hexopyranoside. The acceptor specificity for the D-glucal reaction was identical to that for the alpha-D-glucose 1-phosphate reaction, but the activity Of (D)-glucal was approximately 500 times less than that Of alpha-D-glucose 1-phosphate, using 10 mM substrates. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2006.01.003
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文献信息

  • Reaction on d-glucal by an inverting phosphorylase to synthesize derivatives of 2-deoxy-β-d-arabino-hexopyranosyl-(1→4)-d-glucose (2II-deoxycellobiose)
    作者:Motomitsu Kitaoka、Satoru Nomura、Michiteru Yoshida、Kiyoshi Hayashi
    DOI:10.1016/j.carres.2006.01.003
    日期:2006.3
    Four derivatives of 2(11)-deoxycellobiose were synthesized from D-glucal and acceptor sugars (D-glucose, D-xylose, D-mannose, and 2-deoxy-D-arabino-hexose) using a cellobiose phosphorylase from Cellvibrio gilvus. The enzyme was found to be an effective catalyst to synthesize the beta-(1 -> 4) linkage of 2-dcoxy-D-arabhio-hexopyranoside. The acceptor specificity for the D-glucal reaction was identical to that for the alpha-D-glucose 1-phosphate reaction, but the activity Of (D)-glucal was approximately 500 times less than that Of alpha-D-glucose 1-phosphate, using 10 mM substrates. (c) 2006 Elsevier Ltd. All rights reserved.
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