Brühlmann Corinne, Marston Andrew, Hostettmann Kurt, Carrupt Pierre-Alain, Testa Bernard
Laboratoire de Chimie Thérapeutique, Section de Pharmacie Genève-Lausanne, Université de Genève, CH-1211 Genève 4.
Chem Biodivers. 2004 Jun;1(6):819-29. doi: 10.1002/cbdv.200490064.
Acetylcholinesterase (AChE) inhibitors are currently the only approved therapy for the treatment of Alzheimer's disease, only a limited number of drugs are commercially available. A library of non-alkaloidal natural compounds was investigated. To this end, a convenient microtitre plate method for assaying AChE inhibition, which allows a complete kinetic analysis of AChE inhibitors, was developed. Seven active compounds with Ki values in the micromolar range were identified, six of which were xanthones. This is the first report that a promising potential for AChE inhibition exists in such non-nitrogenous natural compounds. Furthermore, four xanthones among these xanthones had already been described as monoamine oxidase (MAO) inhibitors, making then dual AChE/MAO inhibitors of great interest.
乙酰胆碱酯酶(AChE)抑制剂是目前唯一被批准用于治疗阿尔茨海默病的疗法,市面上仅有有限的几种药物可供使用。对一个非生物碱天然化合物库进行了研究。为此,开发了一种便捷的用于测定AChE抑制作用的微量滴定板方法,该方法能够对AChE抑制剂进行完整的动力学分析。鉴定出了七种Ki值处于微摩尔范围内的活性化合物,其中六种是呫吨酮。这是首份关于此类非含氮天然化合物具有AChE抑制潜在前景的报告。此外,这些呫吨酮中的四种已被描述为单胺氧化酶(MAO)抑制剂,这使得它们成为极具吸引力的双重AChE/MAO抑制剂。