Quercetin and Related Chromenone Derivatives as Monoamine Oxidase Inhibitors: Targeting Neurological and Mental Disorders

被引:73
作者
Dhiman, Priyanka [1 ]
Malik, Neelam [1 ]
Sobarzo-Sanchez, Eduardo [2 ,3 ]
Uriarte, Eugenio [4 ,5 ]
Khatkar, Anurag [1 ]
机构
[1] Maharshi Dayanand Univ, Fac Pharmaceut Sci, Rohtak 124001, Haryana, India
[2] Univ Santiago de Compostela, Fac Pharm, Lab Pharmaceut Chem, Campus Vida, Santiago De Compostela 15782, Spain
[3] Univ Cent Chile, Fac Ciencias Salud, Inst Invest & Innovac Salud, Santiago 8370178, Chile
[4] Univ Santiago de Compostela, Fac Farm, Dept Quim Organ, Santiago De Compostela 15782, Spain
[5] Univ Autonoma Chile, Inst Ciencias Quim Aplicadas, Santiago 7500912, Chile
来源
MOLECULES | 2019年 / 24卷 / 03期
关键词
monoamine oxidase; neurodegenerative disorder; mental disorders; quercetin; flavonoids; monoamine oxidase inhibitors; in-silico design; MAO-B INHIBITORS; ALZHEIMERS-DISEASE; HYDROGEN-PEROXIDE; ANXIETY DISORDERS; ACTIVE PRINCIPLES; NATURAL-PRODUCTS; GLOBAL BURDEN; PART I; FLAVONOIDS; ANTIOXIDANT;
D O I
10.3390/molecules24030418
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Monoamine oxidase inhibitions are considered as important targets for the treatment of depression, anxiety, and neurodegenerative disorders, including Alzheimer's and Parkinson's diseases. This has encouraged many medicinal chemistry research groups for the development of most promising selective monoamine oxidase (MAO) inhibitors. A large number of plant isolates also reported for significant MAO inhibition potential in recent years. Differently substituted flavonoids have been prepared and investigated as MAO-A and MAO-B inhibitors. Flavonoid scaffold showed notable antidepressant and neuroprotective properties as revealed by various and established preclinical trials. The current review made an attempt to summarizing and critically evaluating the new findings on the quercetin and related flavonoid derivatives functions as potent MAO isoform inhibitors.
引用
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页数:18
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