Rampa Angela, Montanari Serena, Pruccoli Letizia, Bartolini Manuela, Falchi Federico, Feoli Alessandra, Cavalli Andrea, Belluti Federica, Gobbi Silvia, Tarozzi Andrea, Bisi Alessandra
Department of Pharmacy & Biotechnology, Alma Mater Studiorum-University of Bologna, Via Belmeloro 6, I-40126 Bologna, Italy.
Department for Life Quality Studies, Alma Mater Studiorum-University of Bologna, Corso d'Augusto 237, I-47921 Rimini, Italy.
Future Med Chem. 2017 May;9(8):749-764. doi: 10.4155/fmc-2017-0029. Epub 2017 May 12.
Alzheimer's disease is a still untreatable multifaceted pathology, and drugs able to stop or reverse its progression are urgently needed. In this picture, the recent reformulation of the cholinergic hypothesis renewed the interest for acetylcholinesterase inhibitors. In this paper, a series of naturally inspired chalcone-based carbamates was designed to target cholinesterase enzymes and possibly generate fragments endowed with neuroprotective activity in situ. Results & methodology: All compounds presented in this study showed nanomolar potency for cholinesterase inhibition. Notably, fragment 11d also displayed an interesting neuroprotective profile.
These new derivatives are able to simultaneously modulate different key targets involved in Alzheimer's disease, and could be regarded as promising starting points for the development of disease-modifying drug candidates. [Formula: see text].
阿尔茨海默病是一种仍无法治愈的多方面病理疾病,迫切需要能够阻止或逆转其进展的药物。在此背景下,胆碱能假说的最新重新阐述重新激发了人们对乙酰胆碱酯酶抑制剂的兴趣。在本文中,设计了一系列受天然启发的基于查尔酮的氨基甲酸酯,以靶向胆碱酯酶,并可能原位产生具有神经保护活性的片段。结果与方法:本研究中呈现的所有化合物对胆碱酯酶抑制均表现出纳摩尔效力。值得注意的是,片段11d还展现出有趣的神经保护特性。
这些新衍生物能够同时调节参与阿尔茨海默病的不同关键靶点,可被视为开发疾病修饰候选药物的有前景的起点。[公式:见正文]