Literature DB >> 32116191

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

Su-Min Wu1, Xiao-Yang Qiu1,2, Shu-Juan Liu1, Juan Sun3.   

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. Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.

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Keywords:  FAD; H2O2; Monoamine oxidase inhibitors; bioactivities; heterocyclic compounds; structure-activity relationship.

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Year:  2020        PMID: 32116191     DOI: 10.2174/1389557520666200302114620

Source DB:  PubMed          Journal:  Mini Rev Med Chem        ISSN: 1389-5575            Impact factor:   3.862


  1 in total

1.  Regioselective synthesis of heterocyclic N-sulfonyl amidines from heteroaromatic thioamides and sulfonyl azides.

Authors:  Vladimir Ilkin; Vera Berseneva; Tetyana Beryozkina; Tatiana Glukhareva; Lidia Dianova; Wim Dehaen; Eugenia Seliverstova; Vasiliy Bakulev
Journal:  Beilstein J Org Chem       Date:  2020-12-01       Impact factor: 2.883

  1 in total

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