sr 48692 has been researched along with amiloride hydrochloride, anhydrous in 1 studies
| Studies (sr 48692) | Trials (sr 48692) | Recent Studies (post-2010) (sr 48692) | Studies (amiloride hydrochloride, anhydrous) | Trials (amiloride hydrochloride, anhydrous) | Recent Studies (post-2010) (amiloride hydrochloride, anhydrous) |
|---|---|---|---|---|---|
| 203 | 3 | 36 | 12 | 0 | 5 |
| Protein | Taxonomy | sr 48692 (IC50) | amiloride hydrochloride, anhydrous (IC50) |
|---|---|---|---|
| serine/threonine-protein kinase D1 isoform 2 | Homo sapiens (human) | 6.8848 | |
| serine/threonine-protein kinase PLK1 | Homo sapiens (human) | 6.629 | |
| Estrogen receptor beta | Mus musculus (house mouse) | 6.8848 | |
| Estrogen receptor | Mus musculus (house mouse) | 6.8848 | |
| Muscarinic receptor M1 | Bos taurus (cattle) | 6.8848 |
| 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 | 1 (100.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ | 1 |
1 other study(ies) available for sr 48692 and amiloride hydrochloride, anhydrous
| Article | Year |
|---|---|
Identification of potent Yes1 kinase inhibitors using a library screening approach.
Topics: Binding Sites; Cell Line; Cell Survival; Drug Design; Humans; Hydrogen Bonding; Molecular Docking Simulation; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-yes; Small Molecule Libraries; Structure-Activity Relationship | 2013 |