6-azidohexyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(2-O-acetyl-4,6-O-benzylidene-3-O-(2-O-benzoyl-4,6-O-benzylidene-3-O-(4,6-O-benzylidene-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranoside | 1259035-97-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 6-azidohexyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(2-O-acetyl-4,6-O-benzylidene-3-O-(2-O-benzoyl-4,6-O-benzylidene-3-O-(4,6-O-benzylidene-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranoside
• CAS: 1259035-97-6
• 化学式: C₇₄H₇₉N₃O₂₄
• 分子量: 1394.45
• InChiKey: FUJZBOWMGHALRN-HZJYBEAXSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.49
• 重原子数：
  101.0
• 可旋转键数：
  23.0
• 环数：
  14.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  315.8
• 氢给体数：
  2.0
• 氢受体数：
  25.0

反应信息

• 作为反应物：
  描述：

  6-azidohexyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(2-O-acetyl-4,6-O-benzylidene-3-O-(2-O-benzoyl-4,6-O-benzylidene-3-O-(4,6-O-benzylidene-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranoside 、 ethylthio 2-O-benzoyl-3-O-(2-O-benzoyl-6-O-(2-O-benzoyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-3-O-(2-O-benzoyl-4,6-O-benzylidene-3-O-(4,6-O-benzylidene-2,3-di-O-levulinyl-β-D-glucopyranosyl)-β-D-glucopyranosyl)-4-O-benzyl-β-D-glucopyranosyl)-4,6-O-benzylidene-β-D-glucopyranoside 在 N-碘代丁二酰亚胺 、 三氟甲磺酸 作用下， 以 二氯甲烷 为溶剂， 反应 0.5h， 以89%的产率得到
  参考文献：
  名称：

  Synthesis of β(1,3) oligoglucans exhibiting a Dectin-1 binding affinity and their biological evaluation

  摘要：

  In this report, we describe the synthesis and biological evaluation of beta(1,3) oligosaccharides that contain an aminoalkyl group and their biological evaluation. A 2,3 diol glycoside with a 4,6 benzylidene protecting group was used as an effective glycosyl acceptor for the synthesis of some beta(1,3) linked glycosides. The use of a combination of a linear tetrasaccharide and a branched pentasaccharide as glycosyl donors led to the preparation of beta(1,3) linear octa-to hexadecasaccharides and branched nona-to heptadecasaccharides in good total yields. Measurements of the competitive effects of the oligosaccharides on the binding of a soluble form of Dectin-1 to a solid-supported Schizophyllan (SPG) revealed that the branched heptadecasaccharide and the linear hexadecasaccharides also have binding activity for Dectin-1. In addition, the two oligosaccharides, both of which contain a beta(1,3) hexadecasaccharide backbone, exhibited agonist activity in a luciferase-assisted NF-kappa B assay. STD-NMR analyses of complexes of Dectin-1 and the linear hexadecasaccharides clearly indicate Dectin-1 specifically recognizes the sugar part of the oligosaccharides and not the aminoalkyl chain. (C) 2012 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmc.2012.04.017
• 作为产物：
  描述：

  在 一水合肼 、 溶剂黄146 作用下， 以 四氢呋喃 为溶剂， 反应 0.33h， 以31 mg的产率得到6-azidohexyl 2-O-benzoyl-4,6-O-benzylidene-3-O-(2-O-acetyl-4,6-O-benzylidene-3-O-(2-O-benzoyl-4,6-O-benzylidene-3-O-(4,6-O-benzylidene-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranosyl)-β-D-glucopyranoside
  参考文献：
  名称：

  Synthesis of β(1,3) oligoglucans exhibiting a Dectin-1 binding affinity and their biological evaluation

  摘要：

  In this report, we describe the synthesis and biological evaluation of beta(1,3) oligosaccharides that contain an aminoalkyl group and their biological evaluation. A 2,3 diol glycoside with a 4,6 benzylidene protecting group was used as an effective glycosyl acceptor for the synthesis of some beta(1,3) linked glycosides. The use of a combination of a linear tetrasaccharide and a branched pentasaccharide as glycosyl donors led to the preparation of beta(1,3) linear octa-to hexadecasaccharides and branched nona-to heptadecasaccharides in good total yields. Measurements of the competitive effects of the oligosaccharides on the binding of a soluble form of Dectin-1 to a solid-supported Schizophyllan (SPG) revealed that the branched heptadecasaccharide and the linear hexadecasaccharides also have binding activity for Dectin-1. In addition, the two oligosaccharides, both of which contain a beta(1,3) hexadecasaccharide backbone, exhibited agonist activity in a luciferase-assisted NF-kappa B assay. STD-NMR analyses of complexes of Dectin-1 and the linear hexadecasaccharides clearly indicate Dectin-1 specifically recognizes the sugar part of the oligosaccharides and not the aminoalkyl chain. (C) 2012 Published by Elsevier Ltd.

  DOI：

  10.1016/j.bmc.2012.04.017