erlotinib has been researched along with docetaxel in 2 studies
Studies (erlotinib) | Trials (erlotinib) | Recent Studies (post-2010) (erlotinib) | Studies (docetaxel) | Trials (docetaxel) | Recent Studies (post-2010) (docetaxel) |
---|---|---|---|---|---|
221 | 0 | 180 | 101 | 0 | 33 |
Protein | Taxonomy | erlotinib (IC50) | docetaxel (IC50) |
---|---|---|---|
Tubulin beta-4A chain | Homo sapiens (human) | 0.5 | |
Tubulin beta chain | Homo sapiens (human) | 0.5 | |
Cytochrome P450 3A4 | Homo sapiens (human) | 2 | |
Tubulin alpha-3C chain | Homo sapiens (human) | 0.5 | |
Substance-K receptor | Homo sapiens (human) | 1.563 | |
Tubulin alpha-1B chain | Homo sapiens (human) | 0.5 | |
Tubulin alpha-4A chain | Homo sapiens (human) | 0.5 | |
Tubulin beta-4B chain | Homo sapiens (human) | 0.5 | |
Growth hormone-releasing hormone receptor | Homo sapiens (human) | 0.0001 | |
Tubulin beta-3 chain | Homo sapiens (human) | 0.5 | |
Tubulin beta-2A chain | Homo sapiens (human) | 0.5 | |
Tubulin beta-8 chain | Homo sapiens (human) | 0.5 | |
Tubulin alpha-3E chain | Homo sapiens (human) | 0.5 | |
Tubulin alpha-1A chain | Homo sapiens (human) | 0.5 | |
Tubulin alpha-1C chain | Homo sapiens (human) | 0.5 | |
Tubulin beta-6 chain | Homo sapiens (human) | 0.5 | |
Tubulin beta-2B chain | Homo sapiens (human) | 0.5 | |
Tubulin beta-1 chain | Homo sapiens (human) | 0.5 |
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 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Benfenati, E; Raska, I; Toropov, AA; Toropova, AP | 1 |
Bailey-Downs, LC; Bastian, A; Disch, BC; Dybdal-Hargreaves, NF; Gangjee, A; Hamel, E; Ihnat, M; Mooberry, SL; Raghavan, S; Rohena, CC; Thorpe, JE; Zhang, X | 1 |
2 other study(ies) available for erlotinib and docetaxel
Article | Year |
---|---|
QSPR modeling of octanol/water partition coefficient of antineoplastic agents by balance of correlations.
Topics: Antineoplastic Agents; Models, Chemical; Octanols; Quantitative Structure-Activity Relationship; Water | 2010 |
The design and discovery of water soluble 4-substituted-2,6-dimethylfuro[2,3-d]pyrimidines as multitargeted receptor tyrosine kinase inhibitors and microtubule targeting antitumor agents.
Topics: Aniline Compounds; Animals; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Discovery; Drug Screening Assays, Antitumor; Female; HeLa Cells; Humans; Mice; Mice, Inbred BALB C; Mice, Nude; Microtubules; Neoplasms, Experimental; Protein Kinase Inhibitors; Pyrimidines; Receptor Protein-Tyrosine Kinases; Solubility; Structure-Activity Relationship; Water | 2014 |