Recent advances in the development of selective human MAO-B inhibitors: (Hetero)arylidene-(4-substituted-thiazol-2-yl)hydrazines-Reference-Cited by-同舟云学术

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Recent advances in the development of selective human MAO-B inhibitors: (Hetero)arylidene-(4-substituted-thiazol-2-yl)hydrazines

Published:2012-12 Issue: Volume:58 Page:405-417
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Secci Daniela,Bolasco Adriana,Carradori Simone,D'Ascenzio Melissa,Nescatelli Riccardo,Yáñez Matilde

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference34 articles.

1. Molecular and Mechanistic Properties of the Membrane-Bound Mitochondrial Monoamine Oxidases

2. cDNA cloning of human liver monoamine oxidase A and B: molecular basis of differences in enzymatic properties.

3. Molecular neuroanatomy of human monoamine oxidases A and B revealed by quantitative enzyme radioautography and in situ hybridization histochemistry

4. The effect of age on the activity and molecular properties of human brain monoamine oxidase

5. Monoamine oxidase, brain ageing and degenerative diseases

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1. Design, Synthesis, and Biological Effect Studies of Novel Benzofuran–Thiazolylhydrazone Derivatives as Monoamine Oxidase Inhibitors;ACS Omega;2024-02-29

2. Correlation intensity index-index of ideality of correlation: A hyphenated target function for furtherance of MAO-B inhibitory activity assessment;Computational Biology and Chemistry;2024-02

3. Synthetic strategies of functionalized pyridines and their therapeutic potential as multifunctional anti-Alzheimer's agents;Recent Developments in the Synthesis and Applications of Pyridines;2023

4. Synthesis of new derivatives containing pyridine, investigation of MAO inhibitory activities and molecular docking studies;Zeitschrift für Naturforschung C;2022-07-20

5. Synthesis of novel thiazolyl hydrazone derivatives as potent dual monoamine oxidase-aromatase inhibitors;European Journal of Medicinal Chemistry;2022-02

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