y 27632 has been researched along with pf-562,271 in 1 studies
| Studies (y 27632) | Trials (y 27632) | Recent Studies (post-2010) (y 27632) | Studies (pf-562,271) | Trials (pf-562,271) | Recent Studies (post-2010) (pf-562,271) |
|---|---|---|---|---|---|
| 1,924 | 3 | 891 | 28 | 0 | 25 |
| Protein | Taxonomy | y 27632 (IC50) | pf-562,271 (IC50) |
|---|---|---|---|
| Chain A, Focal adhesion kinase 1 | Homo sapiens (human) | 0.0015 | |
| Androgen receptor | Rattus norvegicus (Norway rat) | 0.014 | |
| Focal adhesion kinase 1 | Homo sapiens (human) | 0.0014 | |
| Protein-tyrosine kinase 2-beta | Homo sapiens (human) | 0.0104 |
| 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 y 27632 and pf-562,271
| 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 |