Page last updated: 2024-09-05
vx-745 and y 27632
vx-745 has been researched along with y 27632 in 1 studies
Compound Research Comparison
Studies (vx-745) | Trials (vx-745) | Recent Studies (post-2010) (vx-745) | Studies (y 27632) | Trials (y 27632) | Recent Studies (post-2010) (y 27632) |
58 | 1 | 35 | 1,924 | 3 | 891 |
Protein Interaction Comparison
Protein | Taxonomy | vx-745 (IC50) | y 27632 (IC50) |
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit | Bos taurus (cattle) | | 6 |
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit | Bos taurus (cattle) | | 6 |
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit | Bos taurus (cattle) | | 6 |
Chain I, cAMP-dependent protein kinase inhibitor alpha | synthetic construct | | 6 |
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit | Bos taurus (cattle) | | 6 |
Chain A, cAMP-dependent protein kinase, alpha-catalytic subunit | Bos taurus (cattle) | | 6 |
Chain I, cAMP-dependent protein kinase inhibitor alpha | synthetic construct | | 6 |
Rho-associated protein kinase 2 | Homo sapiens (human) | | 0.1942 |
Ribosomal protein S6 kinase alpha-5 | Homo sapiens (human) | | 8.3 |
cAMP-dependent protein kinase catalytic subunit alpha | Bos taurus (cattle) | | 6.1 |
C-C motif chemokine 2 | Homo sapiens (human) | | 2.6303 |
Rho-associated protein kinase 1 | Homo sapiens (human) | | 0.3713 |
Serine/threonine-protein kinase N2 | Homo sapiens (human) | | 0.6 |
Rho-associated protein kinase 2 | Bos taurus (cattle) | | 6.1 |
Rho-associated protein kinase 2 | Rattus norvegicus (Norway rat) | | 0.8 |
Research
Studies (1)
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
Authors | Studies |
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ | 1 |
Other Studies
1 other study(ies) available for vx-745 and y 27632
Article | Year |
Identification of potent Yes1 kinase inhibitors using a library screening approach.Bioorganic & medicinal chemistry letters, 2013, Aug-01, Volume: 23, Issue:15
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 |