6-dimethylaminopyridoxal-3,α⁵-di(methoxymethyl ether) | 582322-89-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 6-dimethylaminopyridoxal-3,α⁵-di(methoxymethyl ether)
• 英文别名: 2-(Dimethylamino)-5-(methoxymethoxy)-3-(methoxymethoxymethyl)-6-methylpyridine-4-carbaldehyde；2-(dimethylamino)-5-(methoxymethoxy)-3-(methoxymethoxymethyl)-6-methylpyridine-4-carbaldehyde
• CAS: 582322-89-2
• 化学式: C₁₄H₂₂N₂O₅
• 分子量: 298.339
• InChiKey: VRVMUMKBJIVGIN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.7
• 重原子数：
  21
• 可旋转键数：
  9
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  70.1
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  6-dimethylaminopyridoxal-3,α⁵-di(methoxymethyl ether) 在 盐酸羟胺 、 sodium acetate 作用下， 以 甲醇 、 水 为溶剂， 反应 2.0h， 生成 6-dimethylaminopyridoxime-α⁵-methoxymethyl ether
  参考文献：
  名称：

  Synthesis of a Novel Radical Trapping and Carbonyl Group Trapping Anti-AGE Agent:  A Pyridoxamine Analogue for Inhibiting Advanced Glycation (AGE) and Lipoxidation (ALE) End Products

  摘要：

  [GRAPHICS]Pyridoxamine is known to be an effective inhibitor of both advanced glycation (AGE) and advanced lipoxidation (ALE) end products. The synthesis of a novel multifunctional AGE and ALE inhibitor, 6-dimethylaminopyridoxamine (dmaPM, 11) is described. The 6-dimethylamino substituent increases the radical trapping ability of pyridoxamine's phenolic group. Results obtained during ribose glycations show that both the new dmaPM and a known strong radical trapping agent, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox), prevent intermolecular protein cross-linking more effectively than pyridoxamine (PM).

  DOI：

  10.1021/ol0348147
• 作为产物：
  描述：

  6-dimethylaminopyridoxine-α⁴-(tert-butyldimethylsilyl ether) 在 manganese(IV) oxide 、 四丁基氟化铵 、 N,N-二异丙基乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 、 丙酮 为溶剂， 反应 73.0h， 生成 6-dimethylaminopyridoxal-3,α⁵-di(methoxymethyl ether)
  参考文献：
  名称：

  Synthesis of a Novel Radical Trapping and Carbonyl Group Trapping Anti-AGE Agent:  A Pyridoxamine Analogue for Inhibiting Advanced Glycation (AGE) and Lipoxidation (ALE) End Products

  摘要：

  [GRAPHICS]Pyridoxamine is known to be an effective inhibitor of both advanced glycation (AGE) and advanced lipoxidation (ALE) end products. The synthesis of a novel multifunctional AGE and ALE inhibitor, 6-dimethylaminopyridoxamine (dmaPM, 11) is described. The 6-dimethylamino substituent increases the radical trapping ability of pyridoxamine's phenolic group. Results obtained during ribose glycations show that both the new dmaPM and a known strong radical trapping agent, 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylic acid (Trolox), prevent intermolecular protein cross-linking more effectively than pyridoxamine (PM).

  DOI：

  10.1021/ol0348147