1,5-anhydro-2-azido-2-deoxy-D-galactitol | 1196658-67-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1,5-anhydro-2-azido-2-deoxy-D-galactitol
• 英文别名: (2R,3R,4R,5S)-5-azido-2-(hydroxymethyl)oxane-3,4-diol
• CAS: 1196658-67-9
• 化学式: C₆H₁₁N₃O₄
• 分子量: 189.171
• InChiKey: UNPRDVHWNUYZCM-KCDKBNATSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.5
• 重原子数：
  13
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  84.3
• 氢给体数：
  3
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  3,4,6-tri-O-acetyl-1,5-anhydro-2-azido-2-deoxy-D-galactitol 在 甲醇 、 sodium 作用下， 以100%的产率得到1,5-anhydro-2-azido-2-deoxy-D-galactitol
  参考文献：
  名称：

  Design, synthesis and evaluation of monovalent ligands for the asialoglycoprotein receptor (ASGP-R)

  摘要：

  A series of novel aryl-substituted triazolyl D-galactosamine derivatives was synthesized as ligands for the carbohydrate recognition domain of the major subunit H1 (H1-CRD) of the human asialoglycoprotein receptor (ASGP-R). The compounds were biologically evaluated with a newly developed competitive binding assay, surface plasmon resonance and by a competitive NMR binding experiment. With compound 1b, a new ligand with a twofold improved affinity to the best so far known D-GalNAc was identified. This small, drug-like ligand can be used as targeting device for drug delivery to hepatocytes. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.08.049

文献信息

• Design, synthesis and evaluation of monovalent ligands for the asialoglycoprotein receptor (ASGP-R)
  作者：Daniela Stokmaier、Oleg Khorev、Brian Cutting、Rita Born、Daniel Ricklin、Thomas O.G. Ernst、Fabienne Böni、Kathrin Schwingruber、Martin Gentner、Matthias Wittwer、Morena Spreafico、Angelo Vedani、Said Rabbani、Oliver Schwardt、Beat Ernst

  DOI：10.1016/j.bmc.2009.08.049

  日期：2009.10

  A series of novel aryl-substituted triazolyl D-galactosamine derivatives was synthesized as ligands for the carbohydrate recognition domain of the major subunit H1 (H1-CRD) of the human asialoglycoprotein receptor (ASGP-R). The compounds were biologically evaluated with a newly developed competitive binding assay, surface plasmon resonance and by a competitive NMR binding experiment. With compound 1b, a new ligand with a twofold improved affinity to the best so far known D-GalNAc was identified. This small, drug-like ligand can be used as targeting device for drug delivery to hepatocytes. (C) 2009 Elsevier Ltd. All rights reserved.