| 1187576-79-9

• 分子结构分类: 有机化合物 - 有机盐 - 有机金属盐
• CAS: 1187576-79-9
• 化学式: C₅₆H₁₁₄Br₆S₆Si₃
• 分子量: 1543.6
• InChiKey: WLXGJBRQDIGPEC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  24.5
• 重原子数：
  71.0
• 可旋转键数：
  62.0
• 环数：
  0.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  0.0
• 氢给体数：
  0.0
• 氢受体数：
  6.0

反应信息

• 作为反应物：
  描述：

  、 乙酸酐 、 ω-acetylthiopentyl 4-O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)- 在 sodium methylate 、 吡啶 作用下， 以 甲醇 、 N,N-二甲基甲酰胺 为溶剂， 以61.5%的产率得到
  参考文献：
  名称：

  Syntheses and biological evaluations of carbosilane dendrimers uniformly functionalized with sialyl α(2→3) lactose moieties as inhibitors for human influenza viruses

  摘要：

  A series of carbosilane dendrimers uniformly functionalized with sialyl lactose moieties (Neu5Ac alpha 2 -> 3-Gal beta 1 -> 4Glc) was systematically synthesized, and biological evaluations for anti-influenza virus activity using the glycodendrimers were performed. The results suggested that the glycodendrimers had unique biological activities depending on the form of their core frame, and Dumbbell(1)6-amide type glycoden-drimer 7 showed particularly strong inhibitory activities against human influenza viruses [A/PR/8/34 (H1N1) and A/Aichi/2/68 (H3N2)]. The results suggested that the structure-activity relationship (SAR) on the glycolibrary against various influenza viruses was observed, and dumbbell-shaped dendrimers as supporting carbohydrate moieties were found to be the most suitable core scaffolds in this study. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2009.06.035