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pent-4-enyl 2,6-di-O-acetyl-3-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-α-D-mannopyranoside | 150772-57-9

中文名称
——
中文别名
——
英文名称
pent-4-enyl 2,6-di-O-acetyl-3-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-α-D-mannopyranoside
英文别名
——
pent-4-enyl 2,6-di-O-acetyl-3-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-α-D-mannopyranoside化学式
CAS
150772-57-9
化学式
C57H61NO14
mdl
——
分子量
984.11
InChiKey
SEQFESDPJYOQHR-DHLCXZBKSA-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

物化性质

  • 沸点:
    957.1±65.0 °C(predicted)
  • 密度:
    1.29±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    7.94
  • 重原子数:
    72.0
  • 可旋转键数:
    24.0
  • 环数:
    8.0
  • sp3杂化的碳原子比例:
    0.37
  • 拓扑面积:
    163.82
  • 氢给体数:
    0.0
  • 氢受体数:
    14.0

反应信息

  • 作为反应物:
    描述:
    乙酸酐pent-4-enyl 2,6-di-O-acetyl-3-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-α-D-mannopyranoside甲胺 作用下, 生成 N-[(2S,3R,4R,5R,6R)-4,5-Bis-benzyloxy-2-((2R,3R,4R,5S,6S)-4-benzyloxy-5-hydroxy-2-hydroxymethyl-6-pent-4-enyloxy-tetrahydro-pyran-3-yloxy)-6-benzyloxymethyl-tetrahydro-pyran-3-yl]-acetamide
    参考文献:
    名称:
    Studies Related to Synthesis of Glycophosphatidylinositol Membrane-Bound Protein Anchors. 6. Convergent Assembly of Subunits
    摘要:
    Glycophosphatidylinositol anchors of membrane-bound proteins are thought to comprise a common pentasaccharide core containing mannan, glucosamine, and inositol residues. A synthetic route to this core is described. In addition, the complete heptasaccharide moiety of the rat brain Thy-1 membrane anchor, the first mammalian membrane anchor to be characterized, has been synthesized. In the case of the Thy-1 anchor, the synthetic plan is based on three building blocks comprising glucosamine-inositol, galactosamine-mannose, and trimannan residues. Although glycosyl donors other than n-pentenyl glycosides (NPGs) have been used in preparing each of these building blocks, the final assembly of the heptasaccharide utilizes NPGs as the only glycosyl donors. The mildness of the conditions for these coupling reactions has allowed us to make provisions for subsequent installation of the three phosphodiester units.
    DOI:
    10.1021/ja00110a011
  • 作为产物:
    描述:
    pent-4-enyl 2,6-di-O-acetyl-3-O-benzyl-α-D-mannopyranoside3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl trichloroacetimidate三氟甲磺酸三甲基硅酯 、 4 A molecular sieve 作用下, 以 甲苯 为溶剂, 反应 2.0h, 以79%的产率得到pent-4-enyl 2,6-di-O-acetyl-3-O-benzyl-4-O-(3,4,6-tri-O-benzyl-2-deoxy-2-phthalimido-β-D-galactopyranosyl)-α-D-mannopyranoside
    参考文献:
    名称:
    A ready, convergent synthesis of the heptasaccharide GPI membrane anchor of rat brain Thy-1 glycoprotein
    摘要:
    DOI:
    10.1021/ja00070a048
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