Inhibitors | Comment | Organism | Structure |
---|---|---|---|
1-(4-((5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) amino)piperidin-1-yl)ethan-1-one | 100 nM, 53.9% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
1-(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) piperazin-1-yl)ethan-1-one | 100 nM, 45.3% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
1-(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) piperazin-1-yl)pentane-1,4-dione | 100 nM, 9.5% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
1-(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl) piperazin-1-yl)propan-1-one | 100 nM, 41.7% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
1-(4-acetylphenyl)-3-(1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)azetidin-3-yl)urea | 100 nM, 50.0% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
1-(4-acetylphenyl)-3-(1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)pyrrolidin-3-yl)urea | 100 nM, 75.7% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
2-(4-acetylphenyl)-1-(4-(2-((4-morpholinophenyl)amino)thieno[3,2-d]pyrimidin-4-yl)piperazin-1-yl)ethan-1-one | 100 nM, 68.0% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
4-(2-(4-(2-((4-morpholinophenyl)amino)thieno[3,2-d]pyrimidin-4-yl)piperazin-1-yl)-2-oxoethyl)benzonitrile | 100 nM, 69.4% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
4-(4-(cyclopropylsulfonyl)piperazin-1-yl)-5-methyl-N-(4-morpholinophenyl)pyrimidin-2-amine | 100 nM, 51.7% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
5-methyl-4-(4-(methylsulfonyl)piperazin-1-yl)-N-(4-morpholinophenyl)pyrimidin-2-amine | 100 nM, 16.7% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
8-(1-acetylpiperidin-4-yl)-2-((4-morpholinophenyl)amino)pteridin-7(8H)-one | 100 nM, 16.7% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
cyclopropyl(4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazin-1-yl)methanone | 100 nM, 31.4% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N,N-dimethyl-4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 68.0% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)piperidine-4-carboxamide | 100 nM, 97.0% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-3-((5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)amino)azetidine-1-carboxamide | 100 nM, 16.2% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-3-((5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)amino)pyrrolidine-1-carboxamide | 100 nM, 57.3% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-((5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)amino)piperidine-1-carboxamide | 100 nM, 78.6% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)-5-(trifluoromethyl)pyr-imidin-4-yl)piperazine-1-carboxamide | 100 nM, 82.5% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)-5-nitropyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 97.8 inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)-7-oxopteridin-8(7H)-yl)piperidine-1-carboxamide | 100 nM, 35.9% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(2-((4-morpholinophenyl)amino)quinazolin-4-yl)piperazine-1-carboxamide | 100 nM, 36.0% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(5-amino-2-((4-morpholinophenyl)amino) pyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 67.9% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(5-chloro-2-((4-morpholinophenyl)amino) pyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 98.7% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(5-fluoro-2-((4-morpholinophenyl)amino) pyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 99.3% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)piperazine-1-sulfonamide | 100 nM, 54.5% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide | 2.9 nM, 81.8% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-(6-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 20.9% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-acetylphenyl)-4-[2-[4-(morpholin-4-yl)anilino]pyrimidin-4-yl]piperazine-1-carboxamide | 30 nM,0.7 % inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-cyanophenyl)-1-(5-methyl-2-((4-morpholinophenyl) amino)pyrimidin-4-yl)piperidine-4-carboxamide | 100 nM, 94.3% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-cyanophenyl)-4-(2-((4-morpholinophenyl)amino)quinazolin-4-yl)piperazine-1-carboxamide | 100 nM, 40.5% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-cyanophenyl)-4-(5-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 95.2% inhibition. 28°C, pH not specified in the publication | Homo sapiens | |
N-(4-cyanophenyl)-4-(6-methyl-2-((4-morpholinophenyl)amino)pyrimidin-4-yl)piperazine-1-carboxamide | 100 nM, 15.8% inhibition. 28°C, pH not specified in the publication | Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | P36888 | - |
- |
Synonyms | Comment | Organism |
---|---|---|
FLT3 | - |
Homo sapiens |