5'-iodoindirubin has been researched along with 5-iodoindirubin-3'-monoxime in 3 studies
| Studies (5'-iodoindirubin) | Trials (5'-iodoindirubin) | Recent Studies (post-2010) (5'-iodoindirubin) | Studies (5-iodoindirubin-3'-monoxime) | Trials (5-iodoindirubin-3'-monoxime) | Recent Studies (post-2010) (5-iodoindirubin-3'-monoxime) |
|---|---|---|---|---|---|
| 6 | 0 | 1 | 8 | 0 | 0 |
| Protein | Taxonomy | 5'-iodoindirubin (IC50) | 5-iodoindirubin-3'-monoxime (IC50) |
|---|---|---|---|
| G2/mitotic-specific cyclin-B2 | Homo sapiens (human) | 0.025 | |
| Cyclin-dependent kinase 1 | Homo sapiens (human) | 0.015 | |
| G2/mitotic-specific cyclin-B1 | Homo sapiens (human) | 0.025 | |
| Receptor-type tyrosine-protein kinase FLT3 | Homo sapiens (human) | 0.418 | |
| Glycogen synthase kinase-3 beta | Homo sapiens (human) | 0.009 | |
| Cyclin-dependent-like kinase 5 | Homo sapiens (human) | 0.02 | |
| Cyclin-dependent kinase 5 activator 1 | Homo sapiens (human) | 0.02 | |
| G2/mitotic-specific cyclin-B3 | Homo sapiens (human) | 0.025 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (66.67) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Greengard, P; Leost, M; Magiatis, P; Meijer, L; Mikros, E; Musacchio, A; Myrianthopoulos, V; Pearl, L; Polychronopoulos, P; Roe, SM; Skaltsounis, AL; Tarricone, A | 1 |
| Grundt, P; Jones-Brando, L; Krivogorsky, B; Yolken, R | 1 |
| Choi, SJ; Choi, SU; Han, SY; Kim, YC; Lee, SD; Moon, MJ | 1 |
3 other study(ies) available for 5'-iodoindirubin and 5-iodoindirubin-3'-monoxime
| Article | Year |
|---|---|
Structural basis for the synthesis of indirubins as potent and selective inhibitors of glycogen synthase kinase-3 and cyclin-dependent kinases.
Topics: Cyclin-Dependent Kinases; Glycogen Synthase Kinase 3; Indoles; Models, Molecular; Oximes; Structure-Activity Relationship | 2004 |
Inhibition of Toxoplasma gondii by indirubin and tryptanthrin analogs.
Topics: Animals; Antiprotozoal Agents; Drugs, Chinese Herbal; Indoles; Isatis; Parasitic Sensitivity Tests; Quinazolines; Toxoplasma | 2008 |
Indirubin derivatives as potent FLT3 inhibitors with anti-proliferative activity of acute myeloid leukemic cells.
Topics: Antibiotics, Antineoplastic; Cell Line, Tumor; Cell Proliferation; Humans; Indoles; Leukemia, Myeloid, Acute | 2010 |