Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B-Reference-Cited by-同舟云学术

Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B

Published:2017-01-01 Issue:1 Volume:32 Page:264-270
ISSN:1475-6366
Container-title:Journal of Enzyme Inhibition and Medicinal Chemistry
language:en
Short-container-title:Journal of Enzyme Inhibition and Medicinal Chemistry

Author:

Meleddu Rita¹,Distinto Simona¹,Cirilli Roberto²,Alcaro Stefano³,Yanez Matilde⁴,Sanna Maria Luisa¹,Corona Angela¹,Melis Claudia¹,Bianco Giulia¹,Matyus Peter⁵,Cottiglia Filippo¹,Maccioni Elias¹

Affiliation:

1. Department of Life and Environmental Sciences, University of Cagliari, Cagliari, Italy;

2. Dipartimento del Farmaco, Istituto Superiore di Sanità, Rome, Italy;

3. Dipartimento di Scienze della Salute, Università Magna Græcia di Catanzaro, Catanzaro, Italy;

4. Departamento de Farmacología and Instituto de Farmacia Industrial, Universidad de Santiago de Compostela, Campus Universitario Sur, Santiago de Compostela, Spain;

5. Department of Organic Chemistry, Semmelweis University, Budapest, Hungary

Publisher

Informa UK Limited

Subject

Drug Discovery,Pharmacology,General Medicine

Link

https://tandfonline.com/doi/pdf/10.1080/14756366.2016.1247061

Reference43 articles.

1. Catalytic Mechanism of the Topa Quinone Containing Copper Amine Oxidases

2. Recent developments on the structure–activity relationship studies of MAO inhibitors and their role in different neurological disorders

3. Type A and B Monoamine Oxidase in Age-Related Neurodegenerative Disorders: Their Distinct Roles in Neuronal Death and Survival

4. MONOAMINE OXIDASE: From Genes to Behavior

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