n3-(4-Morpholin-4-yl-phenyl)-1-pyridin-2-yl-1h-[1,2,4]triazole-3,5-diamine

Name: Inhibition of human recombinant FLT3 by radiometric assay
Source: ChEMBL
Target: Receptor-type tyrosine-protein kinase FLT3
External Id: CHEMBL1958984

Name: Selectivity ratio of Ki for SRC to Ki for human recombinant FLT3
Source: ChEMBL
Target: N/A
External Id: CHEMBL1840414

Name: Selectivity ratio of Ki for JNK3 to Ki for human recombinant FLT3
Source: ChEMBL
Target: N/A
External Id: CHEMBL1840413

Name: Selectivity ratio of Ki for CDK2 to Ki for human recombinant FLT3
Source: ChEMBL
Target: N/A
External Id: CHEMBL1839830

Name: Selectivity ratio of Ki for GSK3 to Ki for human recombinant FLT3
Source: ChEMBL
Target: N/A
External Id: CHEMBL1839829

Name: Selectivity ratio of Ki for PKA to Ki for human recombinant FLT3
Source: ChEMBL
Target: N/A
External Id: CHEMBL1839832

Name: Selectivity ratio of Ki for KDR to Ki for human recombinant FLT3
Source: ChEMBL
Target: N/A
External Id: CHEMBL1839831

Name: Cytotoxicity against human primary leukemia cells isolated from acute myeloid leukemi...
Source: ChEMBL
Target: NON-PROTEIN TARGET
External Id: CHEMBL1959553

Name: Selectivity ratio of IC50 for human recombinant c-Kit to IC50 for wild type human rec...
Source: ChEMBL
Target: N/A
External Id: CHEMBL1959552

Name: Displacement of [33P]ATP from human recombinant FLT3 domain after 20 mins by scintill...
Source: ChEMBL
Target: Receptor-type tyrosine-protein kinase FLT3
External Id: CHEMBL1840408