birb 796 has been researched along with rwj 67657 in 3 studies
| Studies (birb 796) | Trials (birb 796) | Recent Studies (post-2010) (birb 796) | Studies (rwj 67657) | Trials (rwj 67657) | Recent Studies (post-2010) (rwj 67657) |
|---|---|---|---|---|---|
| 137 | 5 | 80 | 34 | 4 | 13 |
| Protein | Taxonomy | birb 796 (IC50) | rwj 67657 (IC50) |
|---|---|---|---|
| Mitogen-activated protein kinase 14 | Homo sapiens (human) | 1 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 2 (66.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Anderson, BD; Blanco-Urgoiti, J; Bonjouklian, R; Campbell, RM; de Dios, A; del Prado, M; Giera, DD; Johnson, LM; Lee, PA; Li, LC; López de Uralde, B; Lorite, MJ; Magnus, N; Martín Cabrejas, LM; McCann, DJ; Nevill, CR; Pleite, S; Sánchez, C; Schultz, RM; Shih, C; Vieth, M; Wang, Y; Wolos, JA; York, J | 1 |
| Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ | 1 |
| Bhat, R; Canan, S; Chojnowski, A; Goldberg, R; Hawryluk, N; Khetani, V; Kreiss, T; Mortensen, D; Prorok, M; Rotella, DP; Siekierka, JJ; Tummalapalli, SR; Zeldis, J | 1 |
3 other study(ies) available for birb 796 and rwj 67657
| Article | Year |
|---|---|
Design of potent and selective 2-aminobenzimidazole-based p38alpha MAP kinase inhibitors with excellent in vivo efficacy.
Topics: Administration, Oral; Animals; Anti-Inflammatory Agents; Arthritis, Experimental; Benzimidazoles; Binding Sites; Biological Availability; Collagen; Crystallography, X-Ray; Drug Design; Humans; Lipopolysaccharides; Macrophages, Peritoneal; Mice; Mice, Inbred BALB C; Mitogen-Activated Protein Kinase 14; Models, Molecular; Rats; Tumor Necrosis Factor-alpha | 2005 |
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 |
Discovery of a Stress-Activated Protein Kinase Inhibitor for Lymphatic Filariasis.
Topics: | 2018 |