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2-azido-2-deoxy-α-D-galactopyranosyl-1-phosphoryl 2-acetamido-2-deoxy-6-O-[2-deoxy-2-hexanoylamino-β-D-glucopyranosyl]-α-D-glucopyranose (triethylammonium salt) | 1616559-53-5

中文名称
——
中文别名
——
英文名称
2-azido-2-deoxy-α-D-galactopyranosyl-1-phosphoryl 2-acetamido-2-deoxy-6-O-[2-deoxy-2-hexanoylamino-β-D-glucopyranosyl]-α-D-glucopyranose (triethylammonium salt)
英文别名
——
2-azido-2-deoxy-α-D-galactopyranosyl-1-phosphoryl 2-acetamido-2-deoxy-6-O-[2-deoxy-2-hexanoylamino-β-D-glucopyranosyl]-α-D-glucopyranose (triethylammonium salt)化学式
CAS
1616559-53-5
化学式
C6H15N*C26H46N5O18P
mdl
——
分子量
848.839
InChiKey
MBQQABDROVRQRN-PKPYTUFFSA-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):
    -2.94
  • 重原子数:
    57.0
  • 可旋转键数:
    19.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.94
  • 拓扑面积:
    364.72
  • 氢给体数:
    11.0
  • 氢受体数:
    19.0

反应信息

  • 作为反应物:
    描述:
    2-azido-2-deoxy-α-D-galactopyranosyl-1-phosphoryl 2-acetamido-2-deoxy-6-O-[2-deoxy-2-hexanoylamino-β-D-glucopyranosyl]-α-D-glucopyranose (triethylammonium salt) 在 palladium on activated charcoal 、 氢气 作用下, 以 甲醇 为溶剂, 反应 4.0h, 以98.8%的产率得到2-amino-2-deoxy-α-D-galactopyranosyl-1-phosphoryl 2-acetamido-2-deoxy-6-O-[2-deoxy-2-hexanoylamino-β-D-glucopyranosyl]-α-D-glucopyranose
    参考文献:
    名称:
    Synthesis of Zwitterionic 1,1′-Glycosylphosphodiester: A Partial Structure of Galactosamine-Modified Francisella Lipid A
    摘要:
    Synthesis of a "double glycosidic" phosphodiester comprising anomeric centers of two 2-amino-2-deoxy-sugars is reported. The carbohydrate epitope of Francisella lipid A modified with alpha-D-galactosamine at the anomerically linked phosphate has been stereoselectively prepared and coupled to maleimide-activated bovine serum albumin via an amide-linked thiol-terminated spacer group. H-Phosphonate and phosphoramidite approaches have been explored for the coupling of 4,6-DTBS-2-azido-protected GalN lactol and peracetylated spacer-equipped reducing beta GlcN(1 -> 6)GlcN disaccharide via phosphodiester linkage. Deprotection conditions preserving the integrity of the labile glycosidic zwitterionic phosphodiester were elaborated.
    DOI:
    10.1021/ol501639c
  • 作为产物:
    描述:
    2-azido-3-O-tert-butyldimethylsilyl-4,6-O-di-tert-butylsilylene-2-deoxy-D-galactopyranosyl-1-hydrogenphosphonate (ammonium salt) 在 氟化氢吡啶 作用下, 以 四氢呋喃吡啶甲醇二氯甲烷 为溶剂, 反应 24.33h, 生成 2-azido-2-deoxy-α-D-galactopyranosyl-1-phosphoryl 2-acetamido-2-deoxy-6-O-[2-deoxy-2-hexanoylamino-β-D-glucopyranosyl]-α-D-glucopyranose (triethylammonium salt)
    参考文献:
    名称:
    Synthesis of Zwitterionic 1,1′-Glycosylphosphodiester: A Partial Structure of Galactosamine-Modified Francisella Lipid A
    摘要:
    Synthesis of a "double glycosidic" phosphodiester comprising anomeric centers of two 2-amino-2-deoxy-sugars is reported. The carbohydrate epitope of Francisella lipid A modified with alpha-D-galactosamine at the anomerically linked phosphate has been stereoselectively prepared and coupled to maleimide-activated bovine serum albumin via an amide-linked thiol-terminated spacer group. H-Phosphonate and phosphoramidite approaches have been explored for the coupling of 4,6-DTBS-2-azido-protected GalN lactol and peracetylated spacer-equipped reducing beta GlcN(1 -> 6)GlcN disaccharide via phosphodiester linkage. Deprotection conditions preserving the integrity of the labile glycosidic zwitterionic phosphodiester were elaborated.
    DOI:
    10.1021/ol501639c
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