28 articles for thisTarget
The following articles (labelled with PubMed ID or TBD) are for your review
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Article Title
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Pyrrole: An emerging scaffold for construction of valuable therapeutic agents.
Padmashri Vikhe Patil College
Design, synthesis, and biological evaluation of oxindole derivatives as antidepressive agents.
Manipal College of Pharmaceutical Sciences
Synthesis and evaluation of quinazoline amino acid derivatives as mono amine oxidase (MAO) inhibitors.
Alexandria University
Synthesis, biological investigation and molecular docking study of N-malonyl-1,2-dihydroisoquinoline derivatives as brain specific and shelf-stable MAO inhibitors.
Assiut University
Exploring new selective 3-benzylquinoxaline-based MAO-A inhibitors: design, synthesis, biological evaluation and docking studies.
Alexandria University
Synthesis, molecular modeling studies and selective inhibitory activity against MAO of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives.
Sapienza University of Rome
Synthesis of new 7-oxycoumarin derivatives as potent and selective monoamine oxidase A inhibitors.
National Research Center
Prenylated xanthones from the root bark of Cudrania tricuspidata.
Chungbuk National University
3-(1H-Pyrrol-1-yl)-2-oxazolidinones as reversible, highly potent, and selective inhibitors of monoamine oxidase type A.
Sapienza University of Rome
Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-(1H-pyrrol-3-yl)-2-oxazolidinones.
Sapienza University of Rome
Proposed structural basis of interaction of piperine and related compounds with monoamine oxidases.
University of Cambridge
Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B.
Sapienza University of Rome
Quercetin as the active principle of Hypericum hircinum exerts a selective inhibitory activity against MAO-A: extraction, biological analysis, and computational study.
Sapienza University of Rome
Research progress in pharmacological activities and structure-activity relationships of tetralone scaffolds as pharmacophore and fluorescent skeleton.
Northwest University
Design, Synthesis, and Monoamine Oxidase B Selective Inhibitory Activity of
Osaka University
Structure-activity relationship around PI-2620 highlights the importance of the nitrogen atom position in the tricyclic core.
Ac Immune
Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B.
Sapienza University of Rome
3-[(2-Methyl-1,3-thiazol-4-yl)ethynyl]-pyridine: a potent and highly selective metabotropic glutamate subtype 5 receptor antagonist with anxiolytic activity.
Merck Research Laboratories
Inhibition of amine oxidases activity by 1-acetyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives.
Sapienza University of Rome
Potent selective monoamine oxidase B inhibition by maackiain, a pterocarpan from the roots of Sophora flavescens.
Sunchon National University
Osthenol, a prenylated coumarin, as a monoamine oxidase A inhibitor with high selectivity.
Sunchon National University
A comprehensive review on synthesis and designing aspects of coumarin derivatives as monoamine oxidase inhibitors for depression and Alzheimer's disease.
R.C. Patel Institute of Pharmaceutical Education and Research
Selective inhibitory activity against MAO and molecular modeling studies of 2-thiazolylhydrazone derivatives.
Universit?????? Degli Studi Di Roma "La Sapienza
Synthesis, molecular modeling studies, and selective inhibitory activity against monoamine oxidase of N,N'-bis[2-oxo-2H-benzopyran]-3-carboxamides.
Universit£
Synthesis of some novel potent and selective catechol O-methyltransferase inhibitors.
Orion
New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity.
Sapienza University of Rome