pramipexole has been researched along with candesartan in 2 studies
Studies (pramipexole) | Trials (pramipexole) | Recent Studies (post-2010) (pramipexole) | Studies (candesartan) | Trials (candesartan) | Recent Studies (post-2010) (candesartan) |
---|---|---|---|---|---|
1,103 | 219 | 517 | 1,929 | 412 | 589 |
Protein | Taxonomy | pramipexole (IC50) | candesartan (IC50) |
---|---|---|---|
Epidermal growth factor receptor | Homo sapiens (human) | 3.2769 | |
Receptor tyrosine-protein kinase erbB-2 | Homo sapiens (human) | 5.9472 | |
Aldo-keto reductase family 1 member B1 | Rattus norvegicus (Norway rat) | 3.0652 | |
Cytochrome P450 3A4 | Homo sapiens (human) | 9 | |
Adenosine receptor A3 | Homo sapiens (human) | 1.2199 | |
Cytochrome P450 2C9 | Homo sapiens (human) | 3 | |
Beta-3 adrenergic receptor | Homo sapiens (human) | 4.3 | |
Alpha-1B adrenergic receptor | Rattus norvegicus (Norway rat) | 1.2199 | |
Alpha-2B adrenergic receptor | Homo sapiens (human) | 3.843 | |
Sodium-dependent noradrenaline transporter | Homo sapiens (human) | 3.0652 | |
Thromboxane-A synthase | Homo sapiens (human) | 3.0594 | |
Type-1 angiotensin II receptor | Homo sapiens (human) | 0.0405 | |
Alpha-1A adrenergic receptor | Rattus norvegicus (Norway rat) | 1.2199 |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (50.00) | 29.6817 |
2010's | 1 (50.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Andricopulo, AD; Moda, TL; Montanari, CA | 1 |
Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K | 1 |
1 review(s) available for pramipexole and candesartan
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 |
1 other study(ies) available for pramipexole and candesartan
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 |