gefitinib has been researched along with tiagabine in 3 studies
| Studies (gefitinib) | Trials (gefitinib) | Recent Studies (post-2010) (gefitinib) | Studies (tiagabine) | Trials (tiagabine) | Recent Studies (post-2010) (tiagabine) |
|---|---|---|---|---|---|
| 5,231 | 566 | 2,919 | 571 | 102 | 111 |
| Protein | Taxonomy | gefitinib (IC50) | tiagabine (IC50) |
|---|---|---|---|
| Sodium- and chloride-dependent GABA transporter 1 | Rattus norvegicus (Norway rat) | 2.2107 | |
| Sodium- and chloride-dependent GABA transporter 1 | Homo sapiens (human) | 0.2213 | |
| Sodium- and chloride-dependent GABA transporter 1 | Mus musculus (house mouse) | 0.1968 | |
| Sodium- and chloride-dependent betaine transporter | Mus musculus (house mouse) | 0.27 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Andricopulo, AD; Moda, TL; Montanari, CA | 1 |
| Lombardo, F; Obach, RS; Waters, NJ | 1 |
| Chen, M; Hu, C; Suzuki, A; Thakkar, S; Tong, W; Yu, K | 1 |
1 review(s) available for gefitinib and tiagabine
| 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 gefitinib and tiagabine
| 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 |
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds.
Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding | 2008 |