erlotinib has been researched along with methyl fluorone black in 1 studies
Studies (erlotinib) | Trials (erlotinib) | Recent Studies (post-2010) (erlotinib) | Studies (methyl fluorone black) | Trials (methyl fluorone black) | Recent Studies (post-2010) (methyl fluorone black) |
---|---|---|---|---|---|
221 | 0 | 180 | 12 | 0 | 4 |
Protein | Taxonomy | erlotinib (IC50) | methyl fluorone black (IC50) |
---|---|---|---|
integrase, partial | Human immunodeficiency virus 1 | 0.874 | |
lens epithelium-derived growth factor p75 | Homo sapiens (human) | 0.874 | |
Mcl-1 | Homo sapiens (human) | 33.23 | |
MPI protein | Homo sapiens (human) | 3.55 | |
nonstructural protein 1 | Influenza A virus (A/California/07/2009(H1N1)) | 30.511 | |
tyrosine-protein phosphatase non-receptor type 22 isoform 1 | Homo sapiens (human) | 0.48 | |
Vif | Human immunodeficiency virus 1 | 0.61 | |
Tat | Human immunodeficiency virus 1 | 52.18 | |
DNA dC->dU-editing enzyme APOBEC-3G isoform 1 | Homo sapiens (human) | 0.61 | |
Muscarinic acetylcholine receptor M1 | Rattus norvegicus (Norway rat) | 12.46 | |
Muscarinic acetylcholine receptor M3 | Rattus norvegicus (Norway rat) | 12.46 | |
Muscarinic acetylcholine receptor M4 | Rattus norvegicus (Norway rat) | 12.46 | |
Muscarinic acetylcholine receptor M5 | Rattus norvegicus (Norway rat) | 12.46 | |
Muscarinic acetylcholine receptor M2 | Rattus norvegicus (Norway rat) | 12.46 | |
Integrase | Human immunodeficiency virus 2 | 1.9 | |
Integrase | Human immunodeficiency virus 1 | 1.15 | |
BZLF2 | Human herpesvirus 4 type 2 (Epstein-Barr virus type 2) | 1 |
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 | 0 (0.00) | 24.3611 |
2020's | 1 (100.00) | 2.80 |
Authors | Studies |
---|---|
Choowongkomon, K; Eurtivong, C; Jiwacharoenchai, N; Niwetmarin, W; Ruchirawat, S; Saruengkhanphasit, R; Seetaha, S | 1 |
1 other study(ies) available for erlotinib and methyl fluorone black
Article | Year |
---|---|
Discovery of potent antiproliferative agents from selected oxygen heterocycles as EGFR tyrosine kinase inhibitors from the U.S. National Cancer Institute database by in silico screening and bioactivity evaluation.
Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Dose-Response Relationship, Drug; Drug Discovery; Drug Evaluation, Preclinical; Drug Screening Assays, Antitumor; ErbB Receptors; Heterocyclic Compounds; Humans; Molecular Docking Simulation; Molecular Structure; National Cancer Institute (U.S.); Oxygen; Protein Kinase Inhibitors; Structure-Activity Relationship; United States; Xanthenes | 2022 |