bisindolylmaleimide iv has been researched along with arcyriaflavin a in 3 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (66.67) | 18.2507 |
2000's | 1 (33.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Ajakane, M; Baudet, V; Bellevergue, P; Boissin, P; Boursier, E; Coste, H; Grand-Perret, T; Loriolle, F; Pianetti, P; Toullec, D | 1 |
Buchdunger, E; Furet, P; Kump, W; Lydon, N; Mett, H; Meyer, T; Müller, M; Regenass, U; Rihs, G; Trinks, U | 1 |
Brooks, HB; Considine, E; DeHahn, TB; Dempsey, JA; Li, T; Ogg, CA; Patel, BK; Sanchez-Martinez, C; Schultz, RM; Shih, C; Spencer, CD; Watkins, SA; Zhang, F; Zhu, G | 1 |
3 other study(ies) available for bisindolylmaleimide iv and arcyriaflavin a
Article | Year |
---|---|
The bisindolylmaleimide GF 109203X is a potent and selective inhibitor of protein kinase C.
Topics: Adenosine Triphosphate; Alkaloids; Animals; Blood Platelets; Bombesin; Collagen; DNA; Electrophoresis, Polyacrylamide Gel; Epidermal Growth Factor; Fibroblasts; Humans; Indoles; Maleimides; Mice; Phorbol 12,13-Dibutyrate; Phosphorylation; Platelet Aggregation; Protein Kinase C; Staurosporine; Structure-Activity Relationship; Thymidine; Vimentin | 1991 |
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinase.
Topics: 3T3 Cells; Adenosine Triphosphate; Animals; Antineoplastic Agents; Binding, Competitive; Cells, Cultured; Drug Screening Assays, Antitumor; ErbB Receptors; Female; Humans; Mice; Mice, Inbred BALB C; Phosphorylation; Phthalimides; Proto-Oncogene Proteins c-fos; RNA, Messenger; Structure-Activity Relationship; Tumor Cells, Cultured; Tyrosine | 1994 |
Studies on cyclin-dependent kinase inhibitors: indolo-[2,3-a]pyrrolo[3,4-c]carbazoles versus bis-indolylmaleimides.
Topics: Antineoplastic Agents; Carbazoles; Cell Division; Cell Line, Tumor; Crystallography, X-Ray; Cyclin-Dependent Kinases; Drug Screening Assays, Antitumor; Enzyme Inhibitors; Flow Cytometry; Humans; Molecular Conformation; Pyrroles; Structure-Activity Relationship | 2003 |