BDBM50444241 CHEMBL3093756::US9649309, Compound UNC2881A
SMILES CCCCNc1ncc(C(=O)NCc2ccc(cc2)-n2ccnc2)c(N[C@H]2CC[C@H](O)CC2)n1
InChI Key InChIKey=NPVXOWLPOFYACO-UHFFFAOYSA-N
Data 9 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 9 hits for monomerid = 50444241
Affinity DataIC50: 4.30nMAssay Description:Briefly, activity assays were performed in a 384 well, polypropylene microplate in a final volume of 50 μL of 50 mM Hepes, Ph 7.4 containing 10 ...More data for this Ligand-Target Pair
Affinity DataIC50: 4.30nMAssay Description:Inhibition of Mer kinase (unknown origin) using 5-FAM-EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluidic capillary electrophoresis assayMore data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Briefly, activity assays were performed in a 384 well, polypropylene microplate in a final volume of 50 μL of 50 mM Hepes, Ph 7.4 containing 10 ...More data for this Ligand-Target Pair
Affinity DataIC50: 22nMAssay Description:Inhibition of Mer kinase phosphorylation in human 697 B-ALL cells after 1 hr by Western blot analysisMore data for this Ligand-Target Pair
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
University of North Carolina at Chapel Hill
US Patent
University of North Carolina at Chapel Hill
US Patent
Affinity DataIC50: 55nMAssay Description:Briefly, activity assays were performed in a 384 well, polypropylene microplate in a final volume of 50 μL of 50 mM Hepes, Ph 7.4 containing 10 ...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase receptor TYRO3(Human)
Eshelman School of Pharmacy�Department of Pharmacology�Lineberger Compreh
Curated by ChEMBL
Eshelman School of Pharmacy�Department of Pharmacology�Lineberger Compreh
Curated by ChEMBL
Affinity DataIC50: 250nMAssay Description:Inhibition of Tyro-3 kinase (unknown origin) using 5-FAM-EFPIYDFLPAKKK-CONH2 as substrate after 180 mins by microfluidic capillary electrophoresis as...More data for this Ligand-Target Pair
Affinity DataIC50: 254nMAssay Description:Briefly, activity assays were performed in a 384 well, polypropylene microplate in a final volume of 50 μL of 50 mM Hepes, Ph 7.4 containing 10 ...More data for this Ligand-Target Pair
TargetTyrosine-protein kinase receptor UFO(Human)
Eshelman School of Pharmacy�Department of Pharmacology�Lineberger Compreh
Curated by ChEMBL
Eshelman School of Pharmacy�Department of Pharmacology�Lineberger Compreh
Curated by ChEMBL
Affinity DataIC50: 360nMAssay Description:Inhibition of Axl kinase (unknown origin) using 5-FAM-KKKKEEIYFFF-CONH2 as substrate after 180 mins by microfluidic capillary electrophoresis assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase receptor TYRO3(Human)
Eshelman School of Pharmacy�Department of Pharmacology�Lineberger Compreh
Curated by ChEMBL
Eshelman School of Pharmacy�Department of Pharmacology�Lineberger Compreh
Curated by ChEMBL
Affinity DataIC50: 563nMAssay Description:Briefly, activity assays were performed in a 384 well, polypropylene microplate in a final volume of 50 μL of 50 mM Hepes, Ph 7.4 containing 10 ...More data for this Ligand-Target Pair
