Culbertson Sean M, Enright Gary D, Ingold K U
Steacie Institute for Molecular Sciences, National Research Council Canada, Ottawa, Ontario K1A 0R6, Canada.
Org Lett. 2003 Jul 24;5(15):2659-62. doi: 10.1021/ol0348147.
[structure: see text] 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).
[结构:见正文] 已知吡哆胺是晚期糖基化终产物(AGE)和晚期脂质过氧化终产物(ALE)的有效抑制剂。本文描述了一种新型多功能AGE和ALE抑制剂6-二甲基氨基吡哆胺(dmaPM,11)的合成。6-二甲基氨基取代基增强了吡哆胺酚羟基的自由基捕获能力。核糖糖基化过程中获得的结果表明,新型dmaPM和一种已知的强自由基捕获剂6-羟基-2,5,7,8-四甲基色满-2-羧酸(Trolox)比吡哆胺(PM)更有效地防止分子间蛋白质交联。