Chromone-3-carboxylic acid has been researched along with selegiline in 2 studies
Studies (Chromone-3-carboxylic acid) | Trials (Chromone-3-carboxylic acid) | Recent Studies (post-2010) (Chromone-3-carboxylic acid) | Studies (selegiline) | Trials (selegiline) | Recent Studies (post-2010) (selegiline) |
---|---|---|---|---|---|
6 | 0 | 1 | 2,575 | 319 | 394 |
Protein | Taxonomy | Chromone-3-carboxylic acid (IC50) | selegiline (IC50) |
---|---|---|---|
Cholinesterase | Homo sapiens (human) | 0.0055 | |
Cytochrome P450 3A4 | Homo sapiens (human) | 0.0039 | |
Alpha-2A adrenergic receptor | Homo sapiens (human) | 1.798 | |
Alpha-2B adrenergic receptor | Homo sapiens (human) | 0.376 | |
Amine oxidase [flavin-containing] B | Rattus norvegicus (Norway rat) | 0.2127 | |
Amine oxidase [flavin-containing] A | Rattus norvegicus (Norway rat) | 0.9046 | |
Amine oxidase [flavin-containing] A | Homo sapiens (human) | 1.4408 | |
Adenosine receptor A1 | Rattus norvegicus (Norway rat) | 0.0067 | |
Amine oxidase [flavin-containing] B | Homo sapiens (human) | 0.1001 | |
Type-1 angiotensin II receptor | Sus scrofa (pig) | 0.048 | |
Alpha-synuclein | Homo sapiens (human) | 0.27 | |
Amine oxidase [flavin-containing] B | Bos taurus (cattle) | 1 | |
Sigma intracellular receptor 2 | Rattus norvegicus (Norway rat) | 0.017 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 2 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Alcaro, S; Borges, F; Gaspar, A; Milhazes, N; Orallo, F; Ortuso, F; Uriarte, E; Yáñez, M | 1 |
Borges, F; Fonseca, A; Gaspar, A; Milhazes, N; Reis, J; Uriarte, E; Viña, D | 1 |
2 other study(ies) available for Chromone-3-carboxylic acid and selegiline
Article | Year |
---|---|
Chromone-2- and -3-carboxylic acids inhibit differently monoamine oxidases A and B.
Topics: Binding Sites; Chromones; Computer Simulation; Humans; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Protein Isoforms | 2010 |
Chromone 3-phenylcarboxamides as potent and selective MAO-B inhibitors.
Topics: Animals; Cell Line; Chromones; Humans; Inhibitory Concentration 50; Models, Molecular; Monoamine Oxidase; Monoamine Oxidase Inhibitors; Neurodegenerative Diseases; Protein Isoforms; Structure-Activity Relationship | 2011 |