ag 1295 and d-64406

ag 1295 has been researched along with d-64406 in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Baasner, S; Beckers, T; Böhmer, FD; Botzki, A; Dove, S; Hufsky, H; Kassack, MU; Mahboobi, S; Pongratz, H; Schächtele, C; Sellmer, A; Teller, S; Uberall, F; Uecker, A	1
Böhmer, FD; Cénac, C; Dove, S; Eichhorn, E; Elz, S; Fischer, T; Heidel, F; Höcher, H; Hufsky, H; Mahboobi, S; Pongratz, H; Sellmer, A; Sicker, M; Stocking, C; Trümpler, A; Uecker, A	1

Other Studies

2 other study(ies) available for ag 1295 and d-64406

Article	Year
Bis(1H-2-indolyl)methanones as a novel class of inhibitors of the platelet-derived growth factor receptor kinase. Journal of medicinal chemistry, 2002, Feb-28, Volume: 45, Issue:5 Topics: Animals; Cell Division; DNA; Enzyme Inhibitors; Glycine; Humans; Indoles; Ketones; Kinetics; Models, Molecular; Molecular Structure; Phosphorylation; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 1; Receptors, Fibroblast Growth Factor; Receptors, Platelet-Derived Growth Factor; Structure-Activity Relationship	2002
Novel bis(1H-indol-2-yl)methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase. Journal of medicinal chemistry, 2006, Jun-01, Volume: 49, Issue:11 Topics: Acute Disease; Animals; Antineoplastic Agents; Apoptosis; Binding Sites; Cell Line; Cell Line, Tumor; fms-Like Tyrosine Kinase 3; Humans; In Vitro Techniques; Indoles; Leukemia, Myeloid; Ligands; Mice; Models, Molecular; Phosphorylation; Pyrroles; Receptors, Platelet-Derived Growth Factor; Structure-Activity Relationship	2006

Article

Year

Bis(1H-2-indolyl)methanones as a novel class of inhibitors of the platelet-derived growth factor receptor kinase.

Journal of medicinal chemistry, 2002, Feb-28, Volume: 45, Issue:5

Topics: Animals; Cell Division; DNA; Enzyme Inhibitors; Glycine; Humans; Indoles; Ketones; Kinetics; Models, Molecular; Molecular Structure; Phosphorylation; Receptor Protein-Tyrosine Kinases; Receptor, Fibroblast Growth Factor, Type 1; Receptors, Fibroblast Growth Factor; Receptors, Platelet-Derived Growth Factor; Structure-Activity Relationship

2002

Novel bis(1H-indol-2-yl)methanones as potent inhibitors of FLT3 and platelet-derived growth factor receptor tyrosine kinase.

Journal of medicinal chemistry, 2006, Jun-01, Volume: 49, Issue:11

Topics: Acute Disease; Animals; Antineoplastic Agents; Apoptosis; Binding Sites; Cell Line; Cell Line, Tumor; fms-Like Tyrosine Kinase 3; Humans; In Vitro Techniques; Indoles; Leukemia, Myeloid; Ligands; Mice; Models, Molecular; Phosphorylation; Pyrroles; Receptors, Platelet-Derived Growth Factor; Structure-Activity Relationship

2006