2-(1-(2-(1-methylpyrrolidino)ethyl)-1h-indol-3-yl)maleimide has been researched along with bisindolylmaleimide i in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (33.33) | 18.2507 |
| 2000's | 4 (66.67) | 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 |
| Alessi, DR; Bain, J; Deak, M; Elliott, M; Garrido-Franco, M; Komander, D; Kozikowski, AP; Kular, GS; Prakash, KR; Schüttelkopf, AW; van Aalten, DM | 1 |
| Goekjian, P; Jochum, A; Jung, M; Kunick, C; Marshall, B; Meier, R; Saunders, L; Sippl, W; Trapp, J; Verdin, E | 1 |
| Chau, N; Chircop, M; Gordon, CP; Hill, TA; Mariana, A; McCluskey, A; McGeachie, AB; Odell, LR; Quan, A; Robinson, PJ; Sakoff, JA; Venn-Brown, B | 1 |
| Adler, MR; Botsford, SA; Gronau, RT; Light, DB; Ter Beest, JK | 1 |
| Harrison, RA; Jebe, E; Petrunkina, AM; Töpfer-Petersen, E; Tsolova, M | 1 |
6 other study(ies) available for 2-(1-(2-(1-methylpyrrolidino)ethyl)-1h-indol-3-yl)maleimide and bisindolylmaleimide i
| 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 |
Interactions of LY333531 and other bisindolyl maleimide inhibitors with PDK1.
Topics: 3-Phosphoinositide-Dependent Protein Kinases; Binding Sites; Crystallography, X-Ray; Enzyme Inhibitors; Indoles; Maleimides; Models, Molecular; Protein Kinase C; Protein Serine-Threonine Kinases; Protein Structure, Tertiary; Signal Transduction | 2004 |
Adenosine mimetics as inhibitors of NAD+-dependent histone deacetylases, from kinase to sirtuin inhibition.
Topics: Acetylation; Adenosine; Binding Sites; Cell Line, Tumor; Histone Deacetylase Inhibitors; Histone Deacetylases; Humans; Models, Molecular; Molecular Mimicry; Protein Kinase Inhibitors; Sirtuins; Structure-Activity Relationship; Tubulin | 2006 |
Inhibition of dynamin mediated endocytosis by the dynoles--synthesis and functional activity of a family of indoles.
Topics: Acrylamides; Animals; Cell Line; Cell Survival; Dose-Response Relationship, Drug; Drug Evaluation, Preclinical; Dynamin I; Endocytosis; Enzyme Inhibitors; Humans; Indoles; Mice; Molecular Structure; NIH 3T3 Cells; Small Molecule Libraries; Stereoisomerism; Structure-Activity Relationship | 2009 |
Protein kinase C and regulatory volume decrease in mudpuppy red blood cells.
Topics: 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine; Alkaloids; Animals; Benzophenanthridines; Calcium; Cell Size; Enzyme Inhibitors; Erythrocytes; Gramicidin; Hematocrit; Hypotonic Solutions; Indoles; Ion Channel Gating; Ion Transport; Isoquinolines; Maleimides; Models, Biological; Necturus; Osmotic Fragility; Osmotic Pressure; Patch-Clamp Techniques; Phenanthridines; Potassium Channels; Protein Kinase C; Sulfonamides | 1998 |
Signalling pathways involved in the control of sperm cell volume.
Topics: Animals; Cell Size; Cells, Cultured; Chloride Channels; Colforsin; Cyclic AMP; Dose-Response Relationship, Drug; Enzyme Inhibitors; Indoles; Ion Channels; Male; Maleimides; Marine Toxins; Okadaic Acid; Osmosis; Oxazoles; Papaverine; Phosphoprotein Phosphatases; Protein Kinase C; Signal Transduction; Spermatozoa; Staurosporine; Swine | 2007 |