sorafenib has been researched along with dinaciclib in 5 studies
Studies (sorafenib) | Trials (sorafenib) | Recent Studies (post-2010) (sorafenib) | Studies (dinaciclib) | Trials (dinaciclib) | Recent Studies (post-2010) (dinaciclib) |
---|---|---|---|---|---|
6,520 | 730 | 5,251 | 133 | 12 | 129 |
Protein | Taxonomy | sorafenib (IC50) | dinaciclib (IC50) |
---|---|---|---|
Cyclin-T1 | Homo sapiens (human) | 0.0272 | |
Cyclin-K | Homo sapiens (human) | 0.0227 | |
Cyclin-dependent kinase 1 | Homo sapiens (human) | 0.0162 | |
Cyclin-dependent kinase 4 | Homo sapiens (human) | 0.0742 | |
G2/mitotic-specific cyclin-B1 | Homo sapiens (human) | 0.049 | |
Cyclin-A2 | Homo sapiens (human) | 0.002 | |
G1/S-specific cyclin-D1 | Homo sapiens (human) | 0.119 | |
G1/S-specific cyclin-E1 | Homo sapiens (human) | 0.0028 | |
Cyclin-dependent kinase 2 | Homo sapiens (human) | 0.0074 | |
Aldo-keto reductase family 1 member C3 | Homo sapiens (human) | 0.23 | |
Cyclin-dependent kinase 8 | Homo sapiens (human) | 0.0039 | |
Glycogen synthase kinase-3 alpha | Homo sapiens (human) | 0.414 | |
Glycogen synthase kinase-3 beta | Homo sapiens (human) | 0.324 | |
Cyclin-dependent kinase 7 | Homo sapiens (human) | 0.1273 | |
Cyclin-dependent kinase 9 | Homo sapiens (human) | 0.0227 | |
Cyclin-H | Homo sapiens (human) | 0.17 | |
CDK-activating kinase assembly factor MAT1 | Homo sapiens (human) | 0.17 | |
Cyclin-A1 | Homo sapiens (human) | 0.003 | |
Cyclin-dependent-like kinase 5 | Homo sapiens (human) | 0.011 | |
Heat shock factor protein 1 | Homo sapiens (human) | 0.007 | |
Cyclin-dependent kinase 13 | Homo sapiens (human) | 0.021 | |
Cyclin-dependent kinase 5 activator 1 | Homo sapiens (human) | 0.0219 | |
Cyclin-dependent kinase 12 | Homo sapiens (human) | 0.0323 |
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 | 2 (40.00) | 24.3611 |
2020's | 3 (60.00) | 2.80 |
Authors | Studies |
---|---|
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 |
Bharate, SB; Raghuvanshi, R | 1 |
Caballero, E; García-Cárceles, J; Gil, C; Martínez, A | 1 |
Laufer, S; Pillaiyar, T | 1 |
Deng, M; Huang, F; Jia, C; Liang, H; Lin, N; Xiong, Z; Xu, J; Yao, Z | 1 |
2 review(s) available for sorafenib and dinaciclib
Article | Year |
---|---|
Kinase Inhibitors as Underexplored Antiviral Agents.
Topics: Animals; Antiviral Agents; Drug Repositioning; Humans; Protein Kinase Inhibitors; Virus Diseases; Viruses | 2022 |
Kinases as Potential Therapeutic Targets for Anti-coronaviral Therapy.
Topics: Antiviral Agents; COVID-19; COVID-19 Drug Treatment; Humans; Protein Kinase Inhibitors; SARS-CoV-2; Signal Transduction; Virus Replication | 2022 |
3 other study(ies) available for sorafenib and dinaciclib
Article | Year |
---|---|
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 |
Recent Developments in the Use of Kinase Inhibitors for Management of Viral Infections.
Topics: Antiviral Agents; COVID-19; COVID-19 Drug Treatment; Drug Approval; Drug Repositioning; High-Throughput Screening Assays; Humans; Protein Kinase Inhibitors; SARS-CoV-2; United States; United States Food and Drug Administration; Virus Diseases | 2022 |
Inhibition of cyclin E1 sensitizes hepatocellular carcinoma cells to regorafenib by mcl-1 suppression.
Topics: Animals; Apoptosis; Bridged Bicyclo Compounds, Heterocyclic; Carcinoma, Hepatocellular; Cell Line, Tumor; Cyclic N-Oxides; Cyclin E; Drug Synergism; Flavonoids; Gene Expression Regulation, Neoplastic; Humans; Indolizines; Liver Neoplasms; Male; Mice; Myeloid Cell Leukemia Sequence 1 Protein; Oncogene Proteins; Phenylurea Compounds; Piperidines; Prognosis; Pyridines; Pyridinium Compounds; Sorafenib; STAT3 Transcription Factor; Xenograft Model Antitumor Assays | 2019 |