Institute of Drug Synthesis and Pharmaceutical Processing, School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, China.
Eur J Med Chem. 2011 Dec;46(12):5885-93. doi: 10.1016/j.ejmech.2011.09.051. Epub 2011 Oct 5.
A series of 9-N-substituted berberine derivatives were synthesized and biologically evaluated as antioxidant and inhibitors of acetylcholinesterase (AChE), butyrylcholinesterase and amyloid-β aggregation. Most of these compounds exhibited very good antioxidant activities, inhibitive activities of AChE and amyloid-β aggregation. Among them, compound 8d, (o-methylphenethyl)amino linked at the 9-position of berberine, was found to be a good antioxidant (with 4.05 μM of Trolox equivalents), potent inhibitor of AChE (an IC(50) value of 0.027 μM), and high active inhibitor of amyloid-β aggregation (an IC(50) value of 2.73 μM).
一系列 9-N-取代小檗碱衍生物被合成并进行了生物评价,作为抗氧化剂和乙酰胆碱酯酶(AChE)、丁酰胆碱酯酶和淀粉样蛋白-β聚集的抑制剂。这些化合物大多数都表现出非常好的抗氧化活性、AChE 抑制活性和淀粉样蛋白-β聚集抑制活性。其中,化合物 8d,(邻-甲基苯乙基)氨基连接在小檗碱的 9 位,被发现是一种很好的抗氧化剂(具有 4.05 μM Trolox 当量),对 AChE 有很强的抑制作用(IC50 值为 0.027 μM),并且对淀粉样蛋白-β聚集有很高的抑制活性(IC50 值为 2.73 μM)。