cki 7 has been researched along with 1-amino-4-hydroxyanthraquinone in 1 studies
| Studies (cki 7) | Trials (cki 7) | Recent Studies (post-2010) (cki 7) | Studies (1-amino-4-hydroxyanthraquinone) | Trials (1-amino-4-hydroxyanthraquinone) | Recent Studies (post-2010) (1-amino-4-hydroxyanthraquinone) |
|---|---|---|---|---|---|
| 35 | 0 | 7 | 10 | 0 | 2 |
| Protein | Taxonomy | cki 7 (IC50) | 1-amino-4-hydroxyanthraquinone (IC50) |
|---|---|---|---|
| Mcl-1 | Homo sapiens (human) | 4.3454 | |
| plectin 1 | Homo sapiens (human) | 2.9437 | |
| X-linked inhibitor of apoptosis | Homo sapiens (human) | 0.313 | |
| TPA: protein transporter TIM23 | Saccharomyces cerevisiae S288C | 11.3 | |
| neutrophil cytosol factor 1 | Homo sapiens (human) | 0.39 | |
| protein quaking isoform 1 | Mus musculus (house mouse) | 2.276 | |
| eukaryotic translation initiation factor 4 gamma 1 isoform 4 | Homo sapiens (human) | 25.6529 | |
| eukaryotic translation initiation factor 4E isoform 1 | Mus musculus (house mouse) | 25.6529 | |
| Female germline-specific tumor suppressor gld-1 | Caenorhabditis elegans | 3.0245 | |
| Casein kinase I isoform alpha | Homo sapiens (human) | 4 | |
| Casein kinase I isoform delta | Homo sapiens (human) | 0.66 | |
| BZLF2 | Human herpesvirus 4 type 2 (Epstein-Barr virus type 2) | 3.1 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (100.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Caparrotta, L; Cozza, G; Gianoncelli, A; Meggio, F; Montopoli, M; Moro, S; Pinna, LA; Venerando, A; Zagotto, G | 1 |
1 other study(ies) available for cki 7 and 1-amino-4-hydroxyanthraquinone
| Article | Year |
|---|---|
Identification of novel protein kinase CK1 delta (CK1delta) inhibitors through structure-based virtual screening.
Topics: Anthraquinones; Casein Kinase I; Chemistry, Pharmaceutical; Computer Simulation; Drug Design; Drug Evaluation, Preclinical; Enzyme Inhibitors; Humans; Inhibitory Concentration 50; Molecular Conformation; Phosphorylation; Protein Isoforms; Software; Tyrosine | 2008 |