Departamento de Química e Bioquímica, Faculdade de Ciências, Universidade do Porto, Rua Campo Alegre 687, 4169 - 007 Porto, Portugal.
Mini Rev Med Chem. 2012 Sep 1;12(10):907-19. doi: 10.2174/138955712802762301.
Parkinson's disease (PD) is one of the most common neurodegenerative disorders. The role of monoamine oxidase (MAO) inhibitors has expanded in the PD treatment. The present review will summarize the current structureactivity relationship information available on MAOs inhibitors of unrelated families of compounds of oxygen heterocyclic type based on coumarin, chromone and chalcone scaffolds. As the current hitting-one-target therapeutic strategy has been proved to be quite inefficient in PD, this review will also discuss about the development of multi-target drugs, in which MAO inhibition plays a counter-part, as a novel and promising treatment approach for PD.
帕金森病(PD)是最常见的神经退行性疾病之一。单胺氧化酶(MAO)抑制剂在 PD 治疗中的作用不断扩大。本综述将总结基于香豆素、色酮和查尔酮骨架的氧杂环型无关家族化合物的 MAO 抑制剂的现有构效关系信息。由于目前的单一靶点治疗策略已被证明在 PD 中效率不高,因此本综述还将讨论多靶点药物的开发,其中 MAO 抑制作为一个新的、有前途的 PD 治疗方法,起到了重要作用。