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tetradecyl 4-O-(4-O-(2-acetoamide-3-O-(3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-2-deoxy-β-D-galactopyranoside)-3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-β-D-glucopyranoside | 1093982-50-3

中文名称
——
中文别名
——
英文名称
tetradecyl 4-O-(4-O-(2-acetoamide-3-O-(3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-2-deoxy-β-D-galactopyranoside)-3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-β-D-glucopyranoside
英文别名
(2S,4S,5R,6R)-5-acetamido-2-[(2R,3R,4S,5S,6R)-2-[(2S,3R,4R,5R,6R)-3-acetamido-2-[(2R,3S,4R,5R,6S)-4-[(2S,4S,5R,6R)-5-acetamido-6-[(1S,2R)-2-[(2S,4S,5R,6R)-5-acetamido-6-[(1S,2R)-2-[(2S,4S,5R,6R)-5-acetamido-2-carboxy-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxan-2-yl]oxy-1,3-dihydroxypropyl]-2-carboxy-4-hydroxyoxan-2-yl]oxy-1,3-dihydroxypropyl]-2-carboxy-4-hydroxyoxan-2-yl]oxy-6-[(2R,3S,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-tetradecoxyoxan-3-yl]oxy-5-hydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxy-6-[(1S,2R)-2-[(2S,4S,5R,6R)-5-acetamido-2-carboxy-4-hydroxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxan-2-yl]oxy-1,3-dihydroxypropyl]-4-hydroxyoxane-2-carboxylic acid
tetradecyl 4-O-(4-O-(2-acetoamide-3-O-(3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-2-deoxy-β-D-galactopyranoside)-3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-β-D-glucopyranoside化学式
CAS
1093982-50-3
化学式
C95H158N6O61
mdl
——
分子量
2360.3
InChiKey
UVBKMROJLNJMME-SHTVWNMQSA-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):
    -13.6
  • 重原子数:
    162
  • 可旋转键数:
    60
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.88
  • 拓扑面积:
    1070
  • 氢给体数:
    38
  • 氢受体数:
    61

反应信息

  • 作为产物:
    描述:
    tetradecyl 4-O-(4-O-(2-acetoamide-3-O-(6-O-benzyl-3-O-(5-acetoamide-9-O-benzyl-3,5-dideoxy-8-O-(5-acetoamide-9-O-benzyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-4,6-di-O-benzyl-2-deoxy-β-D-galactopyranoside)-6-O-benzyl-3-O-(5-acetoamide-9-O-benzyl-3,5-dideoxy-8-O-(5-acetoamide-9-O-benzyl-3,5-dideoxy-8-O-(5-acetoamide-9-O-benzyl-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-2,3,6-tri-O-Bn-β-D-glucopyranoside 在 palladium dihydroxide氢气 作用下, 以 甲醇 为溶剂, 反应 5.0h, 以5.70 mg的产率得到tetradecyl 4-O-(4-O-(2-acetoamide-3-O-(3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-2-deoxy-β-D-galactopyranoside)-3-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-8-O-(5-acetoamide-3,5-dideoxy-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranosylonate)-D-glycero-α-D-galacto-2-nonulopyranoylonate)-β-D-galactopyranoside)-β-D-glucopyranoside
    参考文献:
    名称:
    An Efficient Convergent Synthesis of GP1c Ganglioside Epitope
    摘要:
    In this report, we describe an efficient convergent synthesis of the GP1c glycolipid epitope, which is one of the most complex c-series gangliosides. The alpha(2,3) and alpha(2,8) sialylations were accomplished by use of 5N,4O-carbonyl and 7,8-O-isopropyliden as well as 5N,4O-carbonyl- and 7,8-di-O-chloroacetyl-protected sialyl donors in good yields with excellent alpha-selectivity, respectively. The two sialyl donors enable synthesis of the di- and trisialylgalactosides by simple glycosylation and deprotection. We synthesized the protected GP1c glycolipid epitope, which is a compact, rigid, branched structure, via direct coupling of tetarasaccharide and pentasaccharide units.
    DOI:
    10.1021/ja807482t
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