(2S,4S,5R)-5-[(2R,4S,5R)-5-[(2R,4S,5R)-3,4-dihydroxy-5-[(2R,4R,5R)-4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(2-hydroxyethoxymethyl)oxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,4-triol

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S,4S,5R)-5-[(2R,4S,5R)-5-[(2R,4S,5R)-3,4-dihydroxy-5-[(2R,4R,5R)-4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydroxy-6-(2-hydroxyethoxymethyl)oxan-2-yl]oxy-6-(hydroxymethyl)oxane-2,3,4-triol
• 化学式: C₂₉H₅₂O₂₃
• 分子量: 768.7
• InChiKey: UWZDLCWCJQHFRB-WAEZGTDSSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -9.3
• 重原子数：
  52
• 可旋转键数：
  17
• 环数：
  4.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  355
• 氢给体数：
  13
• 氢受体数：
  23

文献信息

• Method for Manufacturing Hydroxyethyl Starch Derivatives
  申请人：SERUMWERK BERNBURG AG

  公开号：US20140128594A1

  公开（公告）日：2014-05-08

  A method for manufacturing a modified hydroxyethyl starch carrying a heptonic acid residue on at least one of its termini is disclosed. Within this method, the following steps are carried out: a) dissolving hydroxyethyl starch in water, b) adjusting the pH value to a value of 8.0 to 10.0, c) adding a cyanide compound to the hydroxyethyl starch solution, heating the solution to a temperature of 80 to 99° C. and keeping it at this temperature for a first time period, and d) adjusting the pH value to a value of 2.0 to 4.0, bringing the solution to a temperature of 50 to 90° C. and keeping it at this temperature for a second time period.
• US9181353B2
  申请人：——

  公开号：US9181353B2

  公开（公告）日：2015-11-10
• US9631032B2
  申请人：——

  公开号：US9631032B2

  公开（公告）日：2017-04-25