2-(4-morpholinyl)-4h-1-benzopyran-4-one has been researched along with 2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one in 4 studies
*2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one: specific inhibitor of phosphatidylinositol 3-kinase; structure in first source [MeSH]
*2-(4-morpholinyl)-8-phenyl-4H-1-benzopyran-4-one: specific inhibitor of phosphatidylinositol 3-kinase; structure in first source [MeSH]
| Studies (2-(4-morpholinyl)-4h-1-benzopyran-4-one) | Trials (2-(4-morpholinyl)-4h-1-benzopyran-4-one) | Recent Studies (post-2010) (2-(4-morpholinyl)-4h-1-benzopyran-4-one) | Studies (2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one) | Trials (2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one) | Recent Studies (post-2010) (2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one) |
|---|---|---|---|---|---|
| 6 | 0 | 0 | 4,823 | 5 | 1,810 |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (75.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Chiosis, G; Rosen, N; Sepp-Lorenzino, L | 1 |
| Golding, BT; Griffin, RJ; Hardcastle, IR; Leahy, JJ; Richardson, C; Rigoreau, L; Smith, GC | 1 |
| Fontana, G; Golding, BT; Griffin, RJ; Guiard, S; Hardcastle, IR; Leahy, JJ; Martin, N; Richardson, C; Rigoreau, L; Smith, GC; Stockley, M | 1 |
| Bardos, J; Cano, C; Golding, BT; Griffin, RJ; Hardcastle, IR; Parveen, N; Payne, SL; Peacock, M; Rodriguez-Aristegui, S | 1 |
4 other study(ies) available for 2-(4-morpholinyl)-4h-1-benzopyran-4-one and 2-(4-morpholinyl)-8-phenyl-4h-1-benzopyran-4-one
| Article | Year |
|---|---|
LY294002-geldanamycin heterodimers as selective inhibitors of the PI3K and PI3K-related family.
Topics: Ataxia Telangiectasia Mutated Proteins; Benzoquinones; Cell Cycle Proteins; Chromones; Dimerization; DNA-Activated Protein Kinase; DNA-Binding Proteins; HSP90 Heat-Shock Proteins; Inhibitory Concentration 50; Lactams, Macrocyclic; Morpholines; Phosphoinositide-3 Kinase Inhibitors; Protein Serine-Threonine Kinases; Quinones; Tumor Suppressor Proteins | 2001 |
Identification of a highly potent and selective DNA-dependent protein kinase (DNA-PK) inhibitor (NU7441) by screening of chromenone libraries.
Topics: Chromones; DNA-Activated Protein Kinase; DNA-Binding Proteins; Enzyme Inhibitors; Molecular Structure; Morpholines; Protein Serine-Threonine Kinases; Structure-Activity Relationship | 2004 |
Selective benzopyranone and pyrimido[2,1-a]isoquinolin-4-one inhibitors of DNA-dependent protein kinase: synthesis, structure-activity studies, and radiosensitization of a human tumor cell line in vitro.
Topics: Benzopyrans; Chromones; DNA-Activated Protein Kinase; DNA-Binding Proteins; Drug Screening Assays, Antitumor; HeLa Cells; Humans; Isoquinolines; Morpholines; Nuclear Proteins; Protein Serine-Threonine Kinases; Pyrimidines; Radiation-Sensitizing Agents; Radiation, Ionizing; Stereoisomerism; Structure-Activity Relationship | 2005 |
Mapping the ATP-binding domain of DNA-dependent protein kinase (DNA-PK) with coumarin- and isocoumarin-derived inhibitors.
Topics: Adenosine Triphosphate; Antineoplastic Agents; Binding Sites; Chromones; Coumarins; DNA-Activated Protein Kinase; Humans; Inhibitory Concentration 50; Isocoumarins; Structure-Activity Relationship | 2010 |