BDBM50556317 CHEMBL4795732
SMILES CCN1CCN(CC1)c1cc(cc(c1)C(F)(F)F)C(=O)Nc1cccc(Nc2ccc3c(OC)cccc3n2)c1
InChI Key InChIKey=OTASYYGEHSXRJI-UHFFFAOYSA-N
Data 5 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 50556317
TargetRAF proto-oncogene serine/threonine-protein kinase(Human)
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Affinity DataIC50: 229nMAssay Description:Inhibition of human CRAF using MEK1 (K97R) as substrate in presence of [gamma-33P]ATP by scintillation counting methodMore data for this Ligand-Target Pair
TargetEpithelial discoidin domain-containing receptor 1(Human)
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Affinity DataIC50: 538nMAssay Description:Inhibition of human DDR1 using KKSRGDYMTMQIG as substrate in presence of [gamma-33P]ATP by scintillation counting methodMore data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor(Human)
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Affinity DataIC50: 1.67E+3nMAssay Description:Inhibition of human TRKA using poly[Glu:Tyr] (4:1) as substrate in presence of [gamma-33P]ATP by scintillation counting methodMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase B-raf(Human)
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Affinity DataIC50: 2.23E+3nMAssay Description:Inhibition of human BRAF using MEK1 (K97R) as substrate in presence of [gamma-33P]ATP by scintillation counting methodMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase B-raf(Human)
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Korea Institute of Science & Technology (Kist)
Curated by ChEMBL
Affinity DataIC50: 888nMAssay Description:Inhibition of human BRAF V600E mutant using MEK1 (K97R) as substrate in presence of [gamma-33P]ATP by scintillation counting methodMore data for this Ligand-Target Pair
