(2S,3R,4R,5R,6S)-3-((2S,3R,4R,5R,6S)-3-Acetylamino-6-carbamoyl-4,5-dihydroxy-tetrahydro-pyran-2-yloxy)-6-((3R,4R,5R,6R)-3-acetylamino-2,5-dihydroxy-6-methyl-tetrahydro-pyran-4-yloxy)-5-formylamino-4-hydroxy-tetrahydro-pyran-2-carboxylic acid

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S,3R,4R,5R,6S)-3-((2S,3R,4R,5R,6S)-3-Acetylamino-6-carbamoyl-4,5-dihydroxy-tetrahydro-pyran-2-yloxy)-6-((3R,4R,5R,6R)-3-acetylamino-2,5-dihydroxy-6-methyl-tetrahydro-pyran-4-yloxy)-5-formylamino-4-hydroxy-tetrahydro-pyran-2-carboxylic acid
• 英文别名: (2S,3R,4R,5R,6S)-3-[(2S,3R,4R,5R,6S)-3-acetamido-6-carbamoyl-4,5-dihydroxyoxan-2-yl]oxy-6-[(3R,4R,5R,6R)-3-acetamido-2,5-dihydroxy-6-methyloxan-4-yl]oxy-5-formamido-4-hydroxyoxane-2-carboxylic acid
• 化学式: C₂₃H₃₆N₄O₁₆
• 分子量: 624.556
• InChiKey: OPLAIWNOUYXZLX-NDGGPHRXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -6
• 重原子数：
  43
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.78
• 拓扑面积：
  315
• 氢给体数：
  10
• 氢受体数：
  16

反应信息

• 作为反应物：
  描述：

  (2S,3R,4R,5R,6S)-3-((2S,3R,4R,5R,6S)-3-Acetylamino-6-carbamoyl-4,5-dihydroxy-tetrahydro-pyran-2-yloxy)-6-((3R,4R,5R,6R)-3-acetylamino-2,5-dihydroxy-6-methyl-tetrahydro-pyran-4-yloxy)-5-formylamino-4-hydroxy-tetrahydro-pyran-2-carboxylic acid 在 sodium tetrahydroborate 作用下， 生成 (2S,3R,4R,5R,6S)-3-((2S,3R,4R,5R,6S)-3-Acetylamino-6-carbamoyl-4,5-dihydroxy-tetrahydro-pyran-2-yloxy)-6-[(1R,2R,3R)-1-((S)-1-acetylamino-2-hydroxy-ethyl)-2,3-dihydroxy-butoxy]-5-formylamino-4-hydroxy-tetrahydro-pyran-2-carboxylic acid
  参考文献：
  名称：

  Vinogradov, Evgeny V.; Knirel, Yuriy A.; Shashkov, Alexander S., Carbohydrate Research, 1987, vol. 170, p. C5 - C8

  摘要：

  DOI：