(4-nitro)phenyl α-L-altrofuranoside | 848310-02-1

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (4-nitro)phenyl α-L-altrofuranoside
• 英文别名: (2S,3R,4R,5S)-2-[(1S)-1,2-dihydroxyethyl]-5-(4-nitrophenoxy)oxolane-3,4-diol
• CAS: 848310-02-1
• 化学式: C₁₂H₁₅NO₈
• 分子量: 301.253
• InChiKey: RMQNVZDXEMOJCW-MTVMDMGHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.4
• 重原子数：
  21
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  145
• 氢给体数：
  4
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  1,2,3,5,6-penta-O-acetyl-α-L-altrofuranose 在 sodium methylate 、 对甲苯磺酸 作用下， 以 甲醇 、 甲苯 为溶剂， 反应 3.0h， 生成 (4-nitro)phenyl α-L-altrofuranoside
  参考文献：
  名称：

  Non-natural aldofuranosides as substrates of a β-glucosidase

  摘要：

  Based on glycosidase inhibitory activities of some known 1,4-iminoalditols, four aldofuranosides, (4-nitro)phenyl beta-D-glucofuranoside, -beta-D-galactofuranoside, -alpha-L-idofuranoside and -alpha-L-altrofuranoside, were identified as possible substrates of glucosidases and galactosidases. Three of them were found to be accepted by the beta-glucosidase from Agrobacterium sp. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetasy.2004.11.027

文献信息

• Non-natural aldofuranosides as substrates of a β-glucosidase
  作者：Andreas Tauss、Peter Greimel、Karen Rupitz、Andreas J. Steiner、Arnold E. Stütz、Stephen G. Withers、Tanja M. Wrodnigg

  DOI：10.1016/j.tetasy.2004.11.027

  日期：2005.1

  Based on glycosidase inhibitory activities of some known 1,4-iminoalditols, four aldofuranosides, (4-nitro)phenyl beta-D-glucofuranoside, -beta-D-galactofuranoside, -alpha-L-idofuranoside and -alpha-L-altrofuranoside, were identified as possible substrates of glucosidases and galactosidases. Three of them were found to be accepted by the beta-glucosidase from Agrobacterium sp. (C) 2004 Elsevier Ltd. All rights reserved.