5-aminopentanyl-3,6-dideoxy-α-L-xylo-hexopyranosyl-(1→3)-3,6-dideoxy-α-L-xylo-hexopyranosyl-(1→6)-α-L-galactopyranosyl-α-D-glucopyranosyl-(1→4)-α-D-galactopyranosyl-(1→3)-2-N-acetyl-β-D-glucopyranoside | 1429920-42-2

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 5-aminopentanyl-3,6-dideoxy-α-L-xylo-hexopyranosyl-(1→3)-3,6-dideoxy-α-L-xylo-hexopyranosyl-(1→6)-α-L-galactopyranosyl-α-D-glucopyranosyl-(1→4)-α-D-galactopyranosyl-(1→3)-2-N-acetyl-β-D-glucopyranoside
• 英文别名: N-[(2R,3R,4R,5S,6R)-2-(5-aminopentoxy)-4-[(2S,3R,4R,5R,6R)-5-[(2R,3R,4S,5R,6R)-4-[(2R,3S,5S,6S)-3,5-dihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3S,5S,6S)-3,5-dihydroxy-6-methyloxan-2-yl]oxymethyl]-3,5-dihydroxyoxan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)oxan-3-yl]acetamide
• CAS: 1429920-42-2
• 化学式: C₃₇H₆₆N₂O₂₂
• 分子量: 890.931
• InChiKey: BTRLIMWOJQVANC-GTJTWQKDSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -6.5
• 重原子数：
  61
• 可旋转键数：
  18
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.97
• 拓扑面积：
  370
• 氢给体数：
  13
• 氢受体数：
  23

反应信息

• 作为产物：
  描述：

  在 氢气 、 palladium(II) hydroxide 作用下， 以 四氢呋喃 、 水 为溶剂， 反应 24.0h， 以5 mg的产率得到5-aminopentanyl-3,6-dideoxy-α-L-xylo-hexopyranosyl-(1→3)-3,6-dideoxy-α-L-xylo-hexopyranosyl-(1→6)-α-L-galactopyranosyl-α-D-glucopyranosyl-(1→4)-α-D-galactopyranosyl-(1→3)-2-N-acetyl-β-D-glucopyranoside
  参考文献：
  名称：

  Total Synthesis of theEscherichia coliO111O-Specific Polysaccharide Repeating Unit

  摘要：

  AbstractThe first total synthesis of the O‐antigen pentasaccharide repeating unit from Gram‐negative bacteria Escherichia coli O111 was achieved starting from four monosaccharide building blocks. Key to the synthetic approach was a bis‐glycosylation reaction to combine trisaccharide 10 and colitose 5. The colitose building block (5) was obtained de novo from non‐carbohydrate precursors. The pentasaccharide was equipped at the reducing end with an amino spacer to provide a handle for subsequent conjugation to a carrier protein in anticipation of immunological studies.

  DOI：

  10.1002/chem.201204394