lapatinib has been researched along with at 7519 in 3 studies
Studies (lapatinib) | Trials (lapatinib) | Recent Studies (post-2010) (lapatinib) | Studies (at 7519) | Trials (at 7519) | Recent Studies (post-2010) (at 7519) |
---|---|---|---|---|---|
1,919 | 305 | 1,442 | 27 | 0 | 24 |
Protein | Taxonomy | lapatinib (IC50) | at 7519 (IC50) |
---|---|---|---|
Cyclin-T1 | Homo sapiens (human) | 0.0093 | |
Cyclin-dependent kinase 14 | Homo sapiens (human) | 0.0198 | |
Cyclin-dependent kinase 1 | Homo sapiens (human) | 0.1729 | |
Cyclin-dependent kinase 4 | Homo sapiens (human) | 0.0939 | |
G2/mitotic-specific cyclin-B1 | Homo sapiens (human) | 0.1682 | |
Cyclin-A2 | Homo sapiens (human) | 0.063 | |
G1/S-specific cyclin-D1 | Homo sapiens (human) | 0.1168 | |
G1/S-specific cyclin-E1 | Homo sapiens (human) | 0.36 | |
Cyclin-dependent kinase 2 | Homo sapiens (human) | 0.0586 | |
G1/S-specific cyclin-D3 | Homo sapiens (human) | 0.153 | |
Glycogen synthase kinase-3 beta | Homo sapiens (human) | 0.2 | |
Cyclin-dependent kinase 7 | Homo sapiens (human) | 2.4 | |
Cyclin-dependent kinase 9 | Homo sapiens (human) | 0.0094 | |
Cyclin-H | Homo sapiens (human) | 2.4 | |
CDK-activating kinase assembly factor MAT1 | Homo sapiens (human) | 2.4 | |
Cyclin-A1 | Homo sapiens (human) | 0.047 | |
Cyclin-dependent kinase 3 | Homo sapiens (human) | 0.36 | |
Cyclin-dependent kinase 6 | Homo sapiens (human) | 0.1775 | |
Cyclin-dependent-like kinase 5 | Homo sapiens (human) | 0.1393 | |
Cyclin-dependent kinase 5 activator 1 | Homo sapiens (human) | 0.1813 | |
Cyclin-Y | Homo sapiens (human) | 0.0198 |
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 | 3 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ciceri, P; Davis, MI; Herrgard, S; Hocker, M; Hunt, JP; Pallares, G; Treiber, DK; Wodicka, LM; Zarrinkar, PP | 1 |
Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ | 1 |
Aiche, S; Bassermann, F; Becker, W; Canevari, G; Casale, E; Depaolini, SR; Ehrlich, HC; Felder, ER; Feuchtinger, A; Garz, AK; Gohlke, BO; Götze, K; Greif, PA; Hahne, H; Heinzlmeir, S; Helm, D; Huenges, J; Jeremias, I; Kayser, G; Klaeger, S; Koch, H; Koenig, PA; Kramer, K; Kuster, B; Médard, G; Meng, C; Petzoldt, S; Polzer, H; Preissner, R; Qiao, H; Reinecke, M; Reiter, K; Rueckert, L; Ruland, J; Ruprecht, B; Schlegl, J; Schmidt, T; Schneider, S; Schoof, M; Spiekermann, K; Tõnisson, N; Vick, B; Vooder, T; Walch, A; Wilhelm, M; Wu, Z; Zecha, J; Zolg, DP | 1 |
3 other study(ies) available for lapatinib and at 7519
Article | Year |
---|---|
Comprehensive analysis of kinase inhibitor selectivity.
Topics: Catalysis; Drug Design; Enzyme Stability; High-Throughput Screening Assays; Humans; Protein Binding; Protein Kinase Inhibitors; Protein Kinases; Proteomics; Signal Transduction; Substrate Specificity | 2011 |
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 |
The target landscape of clinical kinase drugs.
Topics: Animals; Antineoplastic Agents; Cell Line, Tumor; Cytokines; Drug Discovery; fms-Like Tyrosine Kinase 3; Humans; Leukemia, Myeloid, Acute; Lung Neoplasms; Mice; Molecular Targeted Therapy; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Proteomics; Xenograft Model Antitumor Assays | 2017 |