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methyl(2-O-benzoyl-4,6-O-isopropylidene-3-O-methyl-α-L-idopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-α-D-glucopyranoside | 150204-66-3

中文名称
——
中文别名
——
英文名称
methyl(2-O-benzoyl-4,6-O-isopropylidene-3-O-methyl-α-L-idopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-α-D-glucopyranoside
英文别名
——
methyl(2-O-benzoyl-4,6-O-isopropylidene-3-O-methyl-α-L-idopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-α-D-glucopyranoside化学式
CAS
150204-66-3
化学式
C45H46O15
mdl
——
分子量
826.851
InChiKey
XOCXOFOXGHKOEL-XZEYSAQTSA-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):
    5.17
  • 重原子数:
    60.0
  • 可旋转键数:
    13.0
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    169.81
  • 氢给体数:
    0.0
  • 氢受体数:
    15.0

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

  • 作为反应物:
    描述:
    methyl(2-O-benzoyl-4,6-O-isopropylidene-3-O-methyl-α-L-idopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-α-D-glucopyranosidechromium(VI) oxide4-二甲氨基吡啶硫酸溶剂黄146三乙胺 作用下, 以 二氯甲烷丙酮 为溶剂, 反应 12.0h, 生成 (2R,3S,4S,5R,6R)-5-Benzoyloxy-6-((2R,3R,4S,5R,6S)-4,5-bis-benzoyloxy-2-benzoyloxymethyl-6-methoxy-tetrahydro-pyran-3-yloxy)-4-methoxy-3-(4-oxo-pentanoyloxy)-tetrahydro-pyran-2-carboxylic acid
    参考文献:
    名称:
    Identification of a hexasaccharide sequence able to inhibit thrombin and suitable for ‘polymerisation’
    摘要:
    Three hexasaccharides, having from low to very high affinity for antithrombin, were synthesised from disaccharide building block precursors. One of them, methyl(sodium 2,3-di-O-methyl-4-O-sodium sulfonato-alpha-L-idopyranosyluronate)-(1 --> 4)-[(2,3,6-tri-O-sodium sulfonato-alpha-D-glucopyranosyl)-(1 --> 4)-(sodium 2,3-di-O-methyl-alpha-L-idopyranosyluronate)-(1 --> 4)](2)-2,3,6-tri-O-sodium sulfonato-alpha-D-glucopyranoside, obtainable from a single disaccharide building block precursor, constitutes a good starting point for obtaining simple oligosaccharidic heparin mimetics able to inhibit the two coagulation factors thrombin and Factor Xa. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(99)00067-1
  • 作为产物:
    描述:
    methyl 2,3,6-tri-O-benzoyl-α-D-glucopyranoside 、 ethyl 2-O-benzoyl-4,6-O-isopropylidene-3-O-methyl-1-thio-L-idopyranoside 在 N-碘代丁二酰亚胺三氟甲磺酸 、 4 A molecular sieve 作用下, 以 甲苯 为溶剂, 反应 2.0h, 以93%的产率得到methyl(2-O-benzoyl-4,6-O-isopropylidene-3-O-methyl-α-L-idopyranosyl)-(1->4)-2,3,6-tri-O-benzoyl-α-D-glucopyranoside
    参考文献:
    名称:
    Identification of a hexasaccharide sequence able to inhibit thrombin and suitable for ‘polymerisation’
    摘要:
    Three hexasaccharides, having from low to very high affinity for antithrombin, were synthesised from disaccharide building block precursors. One of them, methyl(sodium 2,3-di-O-methyl-4-O-sodium sulfonato-alpha-L-idopyranosyluronate)-(1 --> 4)-[(2,3,6-tri-O-sodium sulfonato-alpha-D-glucopyranosyl)-(1 --> 4)-(sodium 2,3-di-O-methyl-alpha-L-idopyranosyluronate)-(1 --> 4)](2)-2,3,6-tri-O-sodium sulfonato-alpha-D-glucopyranoside, obtainable from a single disaccharide building block precursor, constitutes a good starting point for obtaining simple oligosaccharidic heparin mimetics able to inhibit the two coagulation factors thrombin and Factor Xa. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0008-6215(99)00067-1
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