sodium ((2,3-difluorobenzyl) 5-chloroacetamido-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate | 1209012-99-6

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: sodium ((2,3-difluorobenzyl) 5-chloroacetamido-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate
• 英文别名: sodium;(2R,4S,5R,6R)-5-[(2-chloroacetyl)amino]-6-[(1R,2R)-3-[(4-chlorobenzoyl)amino]-1,2-dihydroxypropyl]-2-[(2,3-difluorophenyl)methoxy]-4-hydroxyoxane-2-carboxylate
• CAS: 1209012-99-6
• 化学式: C₂₅H₂₅Cl₂F₂N₂O₉*Na
• 分子量: 629.374
• InChiKey: JPHKVUJYVHGLIV-QWNWARSQSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  -3.39
• 重原子数：
  41
• 可旋转键数：
  11
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  178
• 氢给体数：
  5
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  methyl ((2,3-difluorobenzyl) 5-chloroacetamido-4,7,8-tri-O-acetyl-9-(4-chloro-benzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate 在 水 、 lithium hydroxide 作用下， 以 四氢呋喃 为溶剂， 以60%的产率得到sodium ((2,3-difluorobenzyl) 5-chloroacetamido-9-(4-chlorobenzamido)-3,5,9-trideoxy-D-glycero-α-D-galacto-2-nonulopyranosid)onate
  参考文献：
  名称：

  Low Molecular Weight Antagonists of the Myelin-Associated Glycoprotein: Synthesis, Docking, and Biological Evaluation

  摘要：

  The Injured adult mammalian central nervous system Is all inhibitory environment for axon regeneration due to specific inhibitors,among them the myelin-associated glycoprotein (MAG), a member of the Siglec family (sialic-acid binding immunoglobulin-like lectin). In earlier Studies, we identified the lead structure5, which shows a 250-fold improved in vitro affinity for MAG compared to the tetrasaccharide binding epitope of GQ1b alpha (1), the best physiological MAG ligand described so far. By modifying the 2- and 5-position, the affinity of 5 could be further improved to the nanomolar range (-> 19a). Docking Studies to a homology model of MAG allowed the rationalization of the experimental binding properties. Finally, pharmacokinetic parameters (stability in the cerebrospinal fluid, logD and Permeation through the BBB) indicate the drug-like properties of the high-affinity antagonist 19a.

  DOI：

  10.1021/jm901517k