pramipexole has been researched along with milnacipran in 3 studies
Studies (pramipexole) | Trials (pramipexole) | Recent Studies (post-2010) (pramipexole) | Studies (milnacipran) | Trials (milnacipran) | Recent Studies (post-2010) (milnacipran) |
---|---|---|---|---|---|
1,103 | 219 | 517 | 473 | 112 | 187 |
1,103 | 219 | 517 | 13 | 1 | 5 |
Protein | Taxonomy | pramipexole (IC50) | milnacipran (IC50) |
---|---|---|---|
Cytochrome P450 2D6 | Homo sapiens (human) | 0.064 | |
Sodium-dependent noradrenaline transporter | Homo sapiens (human) | 5.5 | |
Sodium-dependent serotonin transporter | Homo sapiens (human) | 1.782 | |
Sodium-dependent serotonin transporter | Rattus norvegicus (Norway rat) | 0.125 | |
Sodium-dependent dopamine transporter | Homo sapiens (human) | 6.1 | |
Transporter | Rattus norvegicus (Norway rat) | 0.065 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 2 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Andricopulo, AD; Moda, TL; Montanari, CA | 1 |
Alelyunas, YW; Bui, K; Empfield, JR; McCarthy, D; Pelosi-Kilby, L; Shen, C; Spreen, RC | 1 |
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K | 1 |
1 review(s) available for pramipexole and milnacipran
Article | Year |
---|---|
DILIrank: the largest reference drug list ranked by the risk for developing drug-induced liver injury in humans.
Topics: Chemical and Drug Induced Liver Injury; Databases, Factual; Drug Labeling; Humans; Pharmaceutical Preparations; Risk | 2016 |
2 other study(ies) available for pramipexole and milnacipran
Article | Year |
---|---|
Hologram QSAR model for the prediction of human oral bioavailability.
Topics: Administration, Oral; Biological Availability; Holography; Humans; Models, Biological; Models, Molecular; Molecular Structure; Pharmaceutical Preparations; Pharmacokinetics; Quantitative Structure-Activity Relationship | 2007 |
Experimental solubility profiling of marketed CNS drugs, exploring solubility limit of CNS discovery candidate.
Topics: Central Nervous System Agents; Drug Evaluation, Preclinical; Hydrogen-Ion Concentration; Pharmaceutical Preparations; Solubility | 2010 |