gemcitabine has been researched along with azd 7762 in 3 studies
| 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 |
|---|---|
| Davis, MI; Khan, J; Li, SQ; Patel, PR; Shen, M; Sun, H; Thomas, CJ | 1 |
| Brassil, P; Breed, J; DeGrace, N; Deng, C; Grondine, M; Hird, AW; Ioannidis, S; Janetka, JW; Lyne, PD; Read, JA; Su, Q; Toader, D; Vasbinder, MM; Wang, H; Whitston, D; Yang, B; Yu, Y | 1 |
| Han, Z; Li, Y; Liu, J; Tian, C; Wang, M; Wang, X; Yang, J; Zhang, Z | 1 |
3 other study(ies) available for gemcitabine and azd 7762
| Article | Year |
|---|---|
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 |
Adventures in Scaffold Morphing: Discovery of Fused Ring Heterocyclic Checkpoint Kinase 1 (CHK1) Inhibitors.
Topics: Cell Line, Tumor; Cell Proliferation; Checkpoint Kinase 1; DNA Damage; Drug Discovery; Heterocyclic Compounds; Humans; Indoles; Models, Molecular; Protein Domains; Protein Kinase Inhibitors; Pyridines | 2018 |
Synthesis and biological evaluation of 2,6-disubstituted-9H-purine, 2,4-disubstitued-thieno[3,2-d]pyrimidine and -7H-pyrrolo[2,3-d]pyrimidine analogues as novel CHK1 inhibitors.
Topics: Antineoplastic Agents; Cell Cycle; Cell Proliferation; Checkpoint Kinase 1; Colonic Neoplasms; Drug Screening Assays, Antitumor; HEK293 Cells; HT29 Cells; Humans; Models, Molecular; Protein Kinase Inhibitors; Purines; Pyrimidines; Structure-Activity Relationship | 2018 |