staurosporine has been researched along with mechlorethamine in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| García-Mera, X; González-Díaz, H; Prado-Prado, FJ | 1 |
| Doppler, W; Grunicke, HH; Hofmann, J; Jakob, A; Maly, K; Posch, L; Uberall, F | 1 |
| Grunicke, H; Hofmann, J; Jackman, J; Kohn, KW; O'Connor, PM; Schubert, C; Ueberall, F | 1 |
3 other study(ies) available for staurosporine and mechlorethamine
| Article | Year |
|---|---|
Multi-target spectral moment QSAR versus ANN for antiparasitic drugs against different parasite species.
Topics: Antiparasitic Agents; Molecular Structure; Neural Networks, Computer; Parasitic Diseases; Quantitative Structure-Activity Relationship; Species Specificity; Thermodynamics | 2010 |
Enhancement of the antiproliferative effect of cis-diamminedichloroplatinum(II) and nitrogen mustard by inhibitors of protein kinase C.
Topics: Alkaloids; Animals; Cell Division; Cisplatin; Drug Synergism; Mechlorethamine; Protein Kinase C; Quercetin; Rats; Staurosporine; Tamoxifen; Tetradecanoylphorbol Acetate | 1988 |
The protein kinase C inhibitor ilmofosine (BM 41 440) arrests cells in G2 phase and suppresses CDC2 kinase activation through a mechanism different from that of DNA damaging agents.
Topics: Alkaloids; Antineoplastic Agents; Burkitt Lymphoma; CDC2 Protein Kinase; Cell Cycle; Cell Line; DNA Damage; Dose-Response Relationship, Radiation; Electrophoresis, Polyacrylamide Gel; Enzyme Activation; G2 Phase; Humans; Kinetics; Mechlorethamine; Nocodazole; Phospholipid Ethers; Protein Kinase C; Radiation, Ionizing; Staurosporine; Tumor Cells, Cultured | 1994 |