Proteins > Amine oxidase [flavin-containing] A
Page last updated: 2024-08-07 13:05:44
Amine oxidase [flavin-containing] A
An amine oxidase [flavin-containing] A that is encoded in the genome of cow. [OMA:P21398, PRO:DNx]
Synonyms
EC 1.4.3.4;
Monoamine oxidase type A;
MAO-A
Research
Bioassay Publications (16)
| Timeframe | Studies on this Protein(%) | All Drugs % |
|---|
| pre-1990 | 1 (6.25) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (43.75) | 29.6817 |
| 2010's | 7 (43.75) | 24.3611 |
| 2020's | 1 (6.25) | 2.80 |
Compounds (13)
Drugs with Inhibition Measurements
Drugs with Other Measurements
Exploring new selective 3-benzylquinoxaline-based MAO-A inhibitors: design, synthesis, biological evaluation and docking studies.European journal of medicinal chemistry, , Mar-26, Volume: 93, 2015
Design, synthesis, and biological evaluation of oxindole derivatives as antidepressive agents.Bioorganic & medicinal chemistry letters, , Nov-15, Volume: 25, Issue:22, 2015
Synthesis of new 7-oxycoumarin derivatives as potent and selective monoamine oxidase A inhibitors.Journal of medicinal chemistry, , Dec-13, Volume: 55, Issue:23, 2012
Synthesis, molecular modeling studies and selective inhibitory activity against MAO of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives.European journal of medicinal chemistry, , Volume: 43, Issue:10, 2008
Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B.Bioorganic & medicinal chemistry, , Nov-15, Volume: 16, Issue:22, 2008
Monoamine oxidase isoform-dependent tautomeric influence in the recognition of 3,5-diaryl pyrazole inhibitors.Journal of medicinal chemistry, , Feb-08, Volume: 50, Issue:3, 2007
New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity.Journal of medicinal chemistry, , Mar-08, Volume: 50, Issue:5, 2007
Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B.Journal of medicinal chemistry, , Mar-13, Volume: 46, Issue:6, 2003
Exploring new selective 3-benzylquinoxaline-based MAO-A inhibitors: design, synthesis, biological evaluation and docking studies.European journal of medicinal chemistry, , Mar-26, Volume: 93, 2015
Design, synthesis, and biological evaluation of oxindole derivatives as antidepressive agents.Bioorganic & medicinal chemistry letters, , Nov-15, Volume: 25, Issue:22, 2015
Synthesis and evaluation of quinazoline amino acid derivatives as mono amine oxidase (MAO) inhibitors.Bioorganic & medicinal chemistry, , Jul-01, Volume: 23, Issue:13, 2015
Synthesis, biological investigation and molecular docking study of N-malonyl-1,2-dihydroisoquinoline derivatives as brain specific and shelf-stable MAO inhibitors.European journal of medicinal chemistry, , Mar-26, Volume: 93, 2015
Synthesis of new 7-oxycoumarin derivatives as potent and selective monoamine oxidase A inhibitors.Journal of medicinal chemistry, , Dec-13, Volume: 55, Issue:23, 2012
Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B.Bioorganic & medicinal chemistry, , Nov-15, Volume: 16, Issue:22, 2008
New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity.Journal of medicinal chemistry, , Mar-08, Volume: 50, Issue:5, 2007
Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B.Journal of medicinal chemistry, , Mar-13, Volume: 46, Issue:6, 2003
Synthesis of new 7-oxycoumarin derivatives as potent and selective monoamine oxidase A inhibitors.Journal of medicinal chemistry, , Dec-13, Volume: 55, Issue:23, 2012
Synthesis, molecular modeling studies and selective inhibitory activity against MAO of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives.European journal of medicinal chemistry, , Volume: 43, Issue:10, 2008
Synthesis, structure-activity relationships and molecular modeling studies of new indole inhibitors of monoamine oxidases A and B.Bioorganic & medicinal chemistry, , Nov-15, Volume: 16, Issue:22, 2008
Monoamine oxidase isoform-dependent tautomeric influence in the recognition of 3,5-diaryl pyrazole inhibitors.Journal of medicinal chemistry, , Feb-08, Volume: 50, Issue:3, 2007
New pyrrole inhibitors of monoamine oxidase: synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity.Journal of medicinal chemistry, , Mar-08, Volume: 50, Issue:5, 2007
Simple, potent, and selective pyrrole inhibitors of monoamine oxidase types A and B.Journal of medicinal chemistry, , Mar-13, Volume: 46, Issue:6, 2003
Novel reversible monoamine oxidase A inhibitors: highly potent and selective 3-(1H-pyrrol-3-yl)-2-oxazolidinones.Journal of medicinal chemistry, , Dec-08, Volume: 54, Issue:23, 2011
Synthesis, molecular modeling studies and selective inhibitory activity against MAO of N1-propanoyl-3,5-diphenyl-4,5-dihydro-(1H)-pyrazole derivatives.European journal of medicinal chemistry, , Volume: 43, Issue:10, 2008
Monoamine oxidase isoform-dependent tautomeric influence in the recognition of 3,5-diaryl pyrazole inhibitors.Journal of medicinal chemistry, , Feb-08, Volume: 50, Issue:3, 2007
Quercetin as the active principle of Hypericum hircinum exerts a selective inhibitory activity against MAO-A: extraction, biological analysis, and computational study.Journal of natural products, , Volume: 69, Issue:6, 2006
3-(1H-Pyrrol-1-yl)-2-oxazolidinones as reversible, highly potent, and selective inhibitors of monoamine oxidase type A.Journal of medicinal chemistry, , Mar-14, Volume: 45, Issue:6, 2002