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2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-3,6-di-O-acetyl-α-D-galactopyranosyl-(1->3)-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranosyl phosphate | 1186313-75-6

中文名称
——
中文别名
——
英文名称
2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-3,6-di-O-acetyl-α-D-galactopyranosyl-(1->3)-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranosyl phosphate
英文别名
——
2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-3,6-di-O-acetyl-α-D-galactopyranosyl-(1->3)-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranosyl phosphate化学式
CAS
1186313-75-6
化学式
C36H55N4O23P
mdl
——
分子量
942.819
InChiKey
XYISQPXBSGIQIL-AHSGPIHOSA-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):
    -3.0
  • 重原子数:
    64.0
  • 可旋转键数:
    17.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    360.81
  • 氢给体数:
    6.0
  • 氢受体数:
    21.0

反应信息

  • 作为反应物:
    描述:
    2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-3,6-di-O-acetyl-α-D-galactopyranosyl-(1->3)-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranosyl phosphate 、 disodium undecaprenyl phosphate 在 N,N'-羰基二咪唑 作用下, 以 N,N-二甲基甲酰胺甲醇1,2-二氯乙烷 为溶剂, 反应 78.0h, 以67%的产率得到undecaprenyl 2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-3,6-di-O-acetyl-α-D-galactopyranosyl-(1->3)-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranosyl diphosphate
    参考文献:
    名称:
    Synthesis of undecaprenyl pyrophosphate-linked glycans as donor substrates for bacterial protein N-glycosylation
    摘要:
    Synthesis of undecaprenyl pyrophosphate (Und-PP)-linked glycans is described. Bacterial ([E](3),[Z](7))-undecaprenol was synthesized from trans-geranylgeranyl sulfone and isoprenoid building blocks, which was converted to undecaprenyl phosphate (Und-P). It was coupled with glycosyl phosphates to afford Und-PP-linked glycans, including core trisaccharide of Campylobacter jejuni N-glycan. Our synthetic method for Und-PP-linked glycan would provide various substrates as a useful tool for systematic analysis of bacterial protein N-glycosylation. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.06.032
  • 作为产物:
    描述:
    2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-3,6-di-O-acetyl-α-D-galactopyranosyl-(1->3)-2,4-diacetamido-2,4,6-trideoxy-D-glucopyranoside 、 焦磷酸四苄酯lithium hexamethyldisilazane 作用下, 以 四氢呋喃N,N-二甲基甲酰胺 为溶剂, 反应 1.67h, 以37%的产率得到2-acetamido-2-deoxy-3,4,6-tri-O-acetyl-α-D-galactopyranosyl-(1->4)-2-acetamido-2-deoxy-3,6-di-O-acetyl-α-D-galactopyranosyl-(1->3)-2,4-diacetamido-2,4,6-trideoxy-α-D-glucopyranosyl phosphate
    参考文献:
    名称:
    Synthesis of undecaprenyl pyrophosphate-linked glycans as donor substrates for bacterial protein N-glycosylation
    摘要:
    Synthesis of undecaprenyl pyrophosphate (Und-PP)-linked glycans is described. Bacterial ([E](3),[Z](7))-undecaprenol was synthesized from trans-geranylgeranyl sulfone and isoprenoid building blocks, which was converted to undecaprenyl phosphate (Und-P). It was coupled with glycosyl phosphates to afford Und-PP-linked glycans, including core trisaccharide of Campylobacter jejuni N-glycan. Our synthetic method for Und-PP-linked glycan would provide various substrates as a useful tool for systematic analysis of bacterial protein N-glycosylation. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.06.032
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