pent-4-enyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-acetyl-α-L-rhamnopyranoside | 1239318-76-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: pent-4-enyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-acetyl-α-L-rhamnopyranoside
• CAS: 1239318-76-3
• 化学式: C₂₇H₄₀O₁₄
• 分子量: 588.606
• InChiKey: HPSAIISDPYGBLV-KXKRACGXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  41.0
• 可旋转键数：
  12.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.74
• 拓扑面积：
  168.42
• 氢给体数：
  0.0
• 氢受体数：
  14.0

反应信息

• 作为反应物：
  描述：

  pent-4-enyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-acetyl-α-L-rhamnopyranoside 、 硫代乙酸 在 偶氮二异丁腈 作用下， 以 四氢呋喃 为溶剂， 以93%的产率得到5-thioacetylpentyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-acetyl-α-L-rhamnopyranoside
  参考文献：
  名称：

  Molecular Analysis of Carbohydrate−Antibody Interactions: Case Study Using a Bacillus anthracis Tetrasaccharide

  摘要：

  The process for selecting potent and effective carbohydrate antigens is not well-established. A combination of synthetic glycan microarray screening, surface plasmon resonance analysis, and saturation transfer difference NMR spectroscopy was used to dissect the antibody-binding surface of a carbohydrate antigen, revealing crucial binding elements with atomic-level detail. This analysis takes the first step toward uncovering the rules for structure-based design of carbohydrate antigens.

  DOI：

  10.1021/ja104027w
• 作为产物：
  描述：

  、 乙酸酐 在 4-二甲氨基吡啶 作用下， 以 吡啶 为溶剂， 以38 mg的产率得到pent-4-enyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3,4-di-O-acetyl-α-L-rhamnopyranoside
  参考文献：
  名称：

  Molecular Analysis of Carbohydrate−Antibody Interactions: Case Study Using a Bacillus anthracis Tetrasaccharide

  摘要：

  The process for selecting potent and effective carbohydrate antigens is not well-established. A combination of synthetic glycan microarray screening, surface plasmon resonance analysis, and saturation transfer difference NMR spectroscopy was used to dissect the antibody-binding surface of a carbohydrate antigen, revealing crucial binding elements with atomic-level detail. This analysis takes the first step toward uncovering the rules for structure-based design of carbohydrate antigens.

  DOI：

  10.1021/ja104027w