(2S,2'S,3S,3'S,4S,4'S,5R,5'R,6R,6'R)-6,6'-oxybis(3,4,5-tris(benzyloxy)tetrahydro-2H-pyran-2-carbaldehyde) | 897365-18-3

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: (2S,2'S,3S,3'S,4S,4'S,5R,5'R,6R,6'R)-6,6'-oxybis(3,4,5-tris(benzyloxy)tetrahydro-2H-pyran-2-carbaldehyde)
• CAS: 897365-18-3
• 化学式: C₅₄H₅₄O₁₁
• 分子量: 879.016
• InChiKey: GQMZSPUQAJJPMS-IPCGEZBZSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  8.36
• 重原子数：
  65.0
• 可旋转键数：
  22.0
• 环数：
  8.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  117.21
• 氢给体数：
  0.0
• 氢受体数：
  11.0

反应信息

• 作为反应物：
  描述：

  (2S,2'S,3S,3'S,4S,4'S,5R,5'R,6R,6'R)-6,6'-oxybis(3,4,5-tris(benzyloxy)tetrahydro-2H-pyran-2-carbaldehyde) 在 palladium dihydroxide sodium chlorite 、 disodium hydrogenphosphate 、 草酰氯 、 氢气 、 双氧水 、 三甲基铝 、 sodium hydride 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 水 、 甲苯 、 乙腈 为溶剂， 反应 50.0h， 生成
  参考文献：
  名称：

  Synthesis of trehalose-based compounds and their inhibitory activities against Mycobacterium smegmatis

  摘要：

  The synthesis of a library of trehalose-based compounds has been accomplished, and their activities against mycobacterium smegmatis have been determined. A preliminary structure-activity relationship (SAR) is reported. Despite not having a potent lead, one of the trehalose derivatives displays strong activity when applied with isoniazid (INH), which is known to have low sterilizing activity. The bacteriocidal nature of our compounds against Mycobacterium may be significant for the development of new therapies against tuberculosis. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2004.09.033
• 作为产物：
  描述：

  [(2R,3R,4S,5R,6R)-3,4,5-Tris-benzyloxy-6-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-2-yl]-methanol 在 草酰氯 、 二甲基亚砜 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 (2S,2'S,3S,3'S,4S,4'S,5R,5'R,6R,6'R)-6,6'-oxybis(3,4,5-tris(benzyloxy)tetrahydro-2H-pyran-2-carbaldehyde)
  参考文献：
  名称：

  Synthesis of trehalose-based compounds and their inhibitory activities against Mycobacterium smegmatis

  摘要：

  The synthesis of a library of trehalose-based compounds has been accomplished, and their activities against mycobacterium smegmatis have been determined. A preliminary structure-activity relationship (SAR) is reported. Despite not having a potent lead, one of the trehalose derivatives displays strong activity when applied with isoniazid (INH), which is known to have low sterilizing activity. The bacteriocidal nature of our compounds against Mycobacterium may be significant for the development of new therapies against tuberculosis. (C) 2004 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2004.09.033

文献信息

• 6- C -LINKED TREHALOSE GLYCOLIPIDS
  申请人：[en]VICTORIA LINK LIMITED

  公开号：WO2024105547A1

  公开（公告）日：2024-05-23

  The present invention relates to 6-C-linked trehalose glycolipids of formula (I) with Mincle- mediated adjuvant activity and their applications.