BDBM50444247 CHEMBL3093750::US9649309, Compound UNC2775A
SMILES CCCCNc1ncc(C(=O)Nc2ccccc2OC)c(N[C@H]2CC[C@H](O)CC2)n1
InChI Key InChIKey=OPZZIKZUGSMEPY-UHFFFAOYSA-N
Data 8 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 8 hits for monomerid = 50444247
TargetTyrosine-protein kinase Mer(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: 39nMAssay 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
TargetTyrosine-protein kinase Mer(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: 39nMAssay 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 Mer(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: 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
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: 501nMAssay 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: 1.47E+3nMAssay 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: 1.50E+3nMAssay 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
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: 3.80E+3nMAssay 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: 3.81E+3nMAssay 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
