Synthesis, in vitro, and in silico studies of new derivatives of diphenylpiperazine scaffold: A key substructure for MAO inhibition-Reference-Cited by-同舟云学术

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Synthesis, in vitro, and in silico studies of new derivatives of diphenylpiperazine scaffold: A key substructure for MAO inhibition

Published:2024-02 Issue: Volume:143 Page:107011
ISSN:0045-2068
Container-title:Bioorganic Chemistry
language:en
Short-container-title:Bioorganic Chemistry

Author:

El-Halaby Lamiaa O.^ORCID,El-Husseiny Walaa M.,El-Messery Shahenda M.^ORCID,Goda Fatma E.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry

Reference46 articles.

1. The global burden of neurological disorders: translating evidence into policy;Feigin;Lancet Neurol,2020

2. Monoamine Oxidase Inhibitors: From Classic to New Clinical Approaches;Duarte;Handb Exp Pharmacol,2021

3. 8-Amide and 8-carbamate substitution patterns as modulators of 7-hydroxy-4-methylcoumarin's antidepressant profile: Synthesis, biological evaluation and docking studies;Matos;European Journal of Medicinal Chemistry,2023

4. A critical appraisal of MAO-B inhibitors in the treatment of Parkinson's disease;Jost;J Neural Transm (vienna),2022

5. Overview of the Neuroprotective Effects of the MAO-Inhibiting Antidepressant Phenelzine;Matveychuk;Cell Mol Neurobiol,2022

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis, In-Vitro, In-Vivo screening, and molecular docking of disubstituted aminothiazole derivatives and their selenium nanoparticles as potential antiparkinson agents;Journal of Molecular Structure;2024-11

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