phenserine has been researched along with trazodone in 1 studies
Studies (phenserine) | Trials (phenserine) | Recent Studies (post-2010) (phenserine) | Studies (trazodone) | Trials (trazodone) | Recent Studies (post-2010) (trazodone) |
---|---|---|---|---|---|
88 | 6 | 39 | 1,466 | 295 | 312 |
Protein | Taxonomy | phenserine (IC50) | trazodone (IC50) |
---|---|---|---|
5-hydroxytryptamine receptor 4 | Cavia porcellus (domestic guinea pig) | 0.091 | |
Alpha-2A adrenergic receptor | Homo sapiens (human) | 0.909 | |
D(2) dopamine receptor | Homo sapiens (human) | 4.485 | |
5-hydroxytryptamine receptor 2A | Rattus norvegicus (Norway rat) | 0.017 | |
Alpha-1B adrenergic receptor | Rattus norvegicus (Norway rat) | 0.281 | |
Alpha-2B adrenergic receptor | Homo sapiens (human) | 0.389 | |
Alpha-2C adrenergic receptor | Homo sapiens (human) | 1.942 | |
5-hydroxytryptamine receptor 1A | Rattus norvegicus (Norway rat) | 0.311 | |
Alpha-1D adrenergic receptor | Rattus norvegicus (Norway rat) | 0.281 | |
Alpha-1D adrenergic receptor | Homo sapiens (human) | 0.265 | |
5-hydroxytryptamine receptor 2A | Homo sapiens (human) | 0.1315 | |
5-hydroxytryptamine receptor 2C | Homo sapiens (human) | 0.091 | |
5-hydroxytryptamine receptor 1B | Rattus norvegicus (Norway rat) | 0.311 | |
Sodium-dependent serotonin transporter | Homo sapiens (human) | 0.192 | |
Histamine H1 receptor | Homo sapiens (human) | 0.361 | |
D(3) dopamine receptor | Homo sapiens (human) | 3.743 | |
5-hydroxytryptamine receptor 2B | Homo sapiens (human) | 0.107 | |
Alpha-1A adrenergic receptor | Rattus norvegicus (Norway rat) | 0.281 | |
Sigma non-opioid intracellular receptor 1 | Homo sapiens (human) | 2.203 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Duncton, MA; Emerling, DE; Kelly, MG; Nguyen, MT; Vincent, F | 1 |
1 other study(ies) available for phenserine and trazodone
Article | Year |
---|---|
Mining biologically-active molecules for inhibitors of fatty acid amide hydrolase (FAAH): identification of phenmedipham and amperozide as FAAH inhibitors.
Topics: Amidohydrolases; Carbamates; Dose-Response Relationship, Drug; Drug Design; Enzyme Inhibitors; Humans; Models, Molecular; Molecular Structure; Piperazines; Stereoisomerism; Structure-Activity Relationship | 2009 |