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单杂环化合物作为单胺氧化酶抑制剂:从过去到现在。

Single Heterocyclic Compounds as Monoamine Oxidase Inhibitors: From Past to Present.

机构信息

College of Science & Technology, Ningbo University, Ningbo, 315212, China.

State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China.

出版信息

Mini Rev Med Chem. 2020;20(10):908-920. doi: 10.2174/1389557520666200302114620.

Abstract

Inhibitors of monoamine oxidase (MAO) have shown therapeutic values in a variety of neurodegenerative diseases such as depression, Parkinson's disease and Alzheimer's disease. Heterocyclic compounds exhibit a broad spectrum of biological activities and vital leading compounds for the development of chemical drugs. Herein, we focus on the synthesis and screening of novel single heterocyclic derivatives with MAO inhibitory activities during the past decade. This review covers recent pharmacological advancements of single heterocyclic moiety along with structure- activity relationship to provide better correlation among different structures and their receptor interactions.

摘要

单胺氧化酶(MAO)抑制剂在多种神经退行性疾病中显示出治疗价值,如抑郁症、帕金森病和阿尔茨海默病。杂环化合物表现出广泛的生物活性,是开发化学药物的重要先导化合物。本文重点介绍了过去十年中具有 MAO 抑制活性的新型单杂环衍生物的合成和筛选。本综述涵盖了单杂环部分的最新药理学进展以及构效关系,旨在提供不同结构及其与受体相互作用之间更好的相关性。

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