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3-azidopropyl α-L-arabinofuranosyl-(1->3)-β-D-galactopyranosyl-(1->6)-β-D-galactopyranosyl-(1->6)-[α-L-arabinofuranosyl-(1->3)]-β-D-galactopyranosyl-(1->6)-β-D-galactopyranoside | 1190749-54-2

中文名称
——
中文别名
——
英文名称
3-azidopropyl α-L-arabinofuranosyl-(1->3)-β-D-galactopyranosyl-(1->6)-β-D-galactopyranosyl-(1->6)-[α-L-arabinofuranosyl-(1->3)]-β-D-galactopyranosyl-(1->6)-β-D-galactopyranoside
英文别名
——
3-azidopropyl α-L-arabinofuranosyl-(1->3)-β-D-galactopyranosyl-(1->6)-β-D-galactopyranosyl-(1->6)-[α-L-arabinofuranosyl-(1->3)]-β-D-galactopyranosyl-(1->6)-β-D-galactopyranoside化学式
CAS
1190749-54-2
化学式
C37H63N3O29
mdl
——
分子量
1013.91
InChiKey
BODYIRFCLXMEGE-WIMJLCSOSA-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

反应信息

  • 作为反应物:
    描述:
    3-azidopropyl α-L-arabinofuranosyl-(1->3)-β-D-galactopyranosyl-(1->6)-β-D-galactopyranosyl-(1->6)-[α-L-arabinofuranosyl-(1->3)]-β-D-galactopyranosyl-(1->6)-β-D-galactopyranoside 在 10% palladium on activated carbon 、 氢气 作用下, 以 为溶剂, 反应 2.0h, 以86%的产率得到3-aminopropyl α-L-arabinofuranosyl-(1->3)-β-D-galactopyranosyl-(1->6)-β-D-galactopyranosyl-(1->6)-[α-L-arabinofuranosyl-(1->3)]-β-D-galactopyranosyl-(1->6)-β-D-galactopyranoside
    参考文献:
    名称:
    Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies
    摘要:
    Synthesis of tetra- and hexasaccharides built up from a beta-(1 -> 6)-linked galactopyranosyl backbone with arabinofuranosyl side chains at position 3 and with a 3-aminopropyl spacer related to arabinogalactans is described. These oligosaccharides were prepared for investigation of monoclonal antibodies raised against arabinogalactan proteins (AGPs) from pressed juice of Echinacea purpurea. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2009.04.025
  • 作为产物:
    描述:
    3-azidopropyl 2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)-6-O-acetyl-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-1-thio-β-D-galactopyranosyl-(1->6)-[2,3,5-tri-O-benzoyl-α-L-arabinofuranosyl-(1->3)]-2,4-di-O-benzoyl-β-D-galactopyranosyl-(1->6)-2,3,4-tri-O-benzoyl-β-D-galactopyranoside 在 sodium methylate 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 24.0h, 以86%的产率得到3-azidopropyl α-L-arabinofuranosyl-(1->3)-β-D-galactopyranosyl-(1->6)-β-D-galactopyranosyl-(1->6)-[α-L-arabinofuranosyl-(1->3)]-β-D-galactopyranosyl-(1->6)-β-D-galactopyranoside
    参考文献:
    名称:
    Synthesis of 3,6-branched arabinogalactan-type tetra- and hexasaccharides for characterization of monoclonal antibodies
    摘要:
    Synthesis of tetra- and hexasaccharides built up from a beta-(1 -> 6)-linked galactopyranosyl backbone with arabinofuranosyl side chains at position 3 and with a 3-aminopropyl spacer related to arabinogalactans is described. These oligosaccharides were prepared for investigation of monoclonal antibodies raised against arabinogalactan proteins (AGPs) from pressed juice of Echinacea purpurea. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2009.04.025
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