1-(pent-3-yl) 2-acetamido-2-deoxy-β-D-glucopyranoside | 1402746-24-0

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1-(pent-3-yl) 2-acetamido-2-deoxy-β-D-glucopyranoside
• 英文别名: N-[(2R,3R,4R,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-pentan-3-yloxyoxan-3-yl]acetamide
• CAS: 1402746-24-0
• 化学式: C₁₃H₂₅NO₆
• 分子量: 291.345
• InChiKey: HLTOQPDGIJRCLN-SYLRKERUSA-N

物化性质

• 沸点：
  530.7±50.0 °C(predicted)
• 密度：
  1.22±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.2
• 重原子数：
  20
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  108
• 氢给体数：
  4
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  1-(pent-3-yl) 2-acetamido-2-deoxy-β-D-glucopyranoside 在 吡啶 、 甲醇 、 4-二甲氨基吡啶 、 sodium hypochlorite 、 2,2,6,6-四甲基哌啶氧化物 、 sodium methylate 、 碳酸氢钠 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 potassium bromide 、 sodium hydroxide 作用下， 以 甲醇 、 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 106.0h， 生成 1-(pent-3-yl) 2-acetamido-3-O-acetyl-2,4-dideoxy-α-L-threo-hex-4-enopyranosiduronic acid
  参考文献：
  名称：

  Exploring the Interactions of Unsaturated Glucuronides with Influenza Virus Sialidase

  摘要：

  A series of C3 O-functionalized 2-acetamido-2-deoxy-Delta(4)-beta-D-glucuronides were synthesized to explore noncharge interactions in subsite 2 of the influenza virus sialidase active site. In complex with A/N8 sialidase, the parent compound (C3 OH) inverts its solution conformation to bind with all substituents well positioned in the active site. The parent compound inhibits influenza virus sialidase at a sub-mu M level; the introduction of small alkyl substituents or an acetyl group at C3 is also tolerated.

  DOI：

  10.1021/jm301145k
• 作为产物：
  描述：

  D-GlcNAc 在 吡啶 、 甲醇 、 4-二甲氨基吡啶 、 三氟甲磺酸三甲基硅酯 、 sodium methylate 作用下， 以 二氯甲烷 、 1,2-二氯乙烷 为溶剂， 反应 86.25h， 生成 1-(pent-3-yl) 2-acetamido-2-deoxy-β-D-glucopyranoside
  参考文献：
  名称：

  Exploring the Interactions of Unsaturated Glucuronides with Influenza Virus Sialidase

  摘要：

  A series of C3 O-functionalized 2-acetamido-2-deoxy-Delta(4)-beta-D-glucuronides were synthesized to explore noncharge interactions in subsite 2 of the influenza virus sialidase active site. In complex with A/N8 sialidase, the parent compound (C3 OH) inverts its solution conformation to bind with all substituents well positioned in the active site. The parent compound inhibits influenza virus sialidase at a sub-mu M level; the introduction of small alkyl substituents or an acetyl group at C3 is also tolerated.

  DOI：

  10.1021/jm301145k

文献信息

• Exploring the Interactions of Unsaturated Glucuronides with Influenza Virus Sialidase
  作者：Beenu Bhatt、Raphael Böhm、Philip S. Kerry、Jeffrey C. Dyason、Rupert J. M. Russell、Robin J. Thomson、Mark von Itzstein

  DOI：10.1021/jm301145k

  日期：2012.10.25

  A series of C3 O-functionalized 2-acetamido-2-deoxy-Delta(4)-beta-D-glucuronides were synthesized to explore noncharge interactions in subsite 2 of the influenza virus sialidase active site. In complex with A/N8 sialidase, the parent compound (C3 OH) inverts its solution conformation to bind with all substituents well positioned in the active site. The parent compound inhibits influenza virus sialidase at a sub-mu M level; the introduction of small alkyl substituents or an acetyl group at C3 is also tolerated.