erlotinib has been researched along with mk 0752 in 2 studies
Studies (erlotinib) | Trials (erlotinib) | Recent Studies (post-2010) (erlotinib) | Studies (mk 0752) | Trials (mk 0752) | Recent Studies (post-2010) (mk 0752) |
---|---|---|---|---|---|
221 | 0 | 180 | 12 | 0 | 11 |
Protein | Taxonomy | erlotinib (IC50) | mk 0752 (IC50) |
---|---|---|---|
Presenilin-1 | Homo sapiens (human) | 0.03 | |
Presenilin-2 | Homo sapiens (human) | 0.03 | |
Gamma-secretase subunit APH-1B | Homo sapiens (human) | 0.03 | |
Nicastrin | Homo sapiens (human) | 0.03 | |
Gamma-secretase subunit APH-1A | Homo sapiens (human) | 0.03 | |
Gamma-secretase subunit PEN-2 | Homo sapiens (human) | 0.03 |
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 (50.00) | 24.3611 |
2020's | 1 (50.00) | 2.80 |
Authors | Studies |
---|---|
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ | 1 |
Dranchak, PK; Huang, R; Inglese, J; Lamy, L; Oliphant, E; Queme, B; Tao, D; Wang, Y; Xia, M | 1 |
2 other study(ies) available for erlotinib and mk 0752
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 |
In vivo quantitative high-throughput screening for drug discovery and comparative toxicology.
Topics: Animals; Caenorhabditis elegans; Drug Discovery; High-Throughput Screening Assays; Humans; Proteomics; Small Molecule Libraries | 2023 |