BDBM50664122 CHEMBL6162402

SMILES COc1ccc(CN2C3CC2CN(c2ccc(-c4nc(-c5cnn(C)c5)cc5ncccc45)cn2)C3)cc1C#N

InChI Key InChIKey=AVDOTNJRJLVJBV-UHFFFAOYSA-N

Data  35 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 35 hits for monomerid = 50664122   

TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 0.200nMAssay Description:Inhibition of RET V804L mutant (unknown origin) by FRET-based ZLyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 0.400nMAssay Description:Inhibition of RET M918T mutant (unknown origin) by FRET-based ZLyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 1.80nMAssay Description:Inhibition of RET V804M mutant (unknown origin) by FRET-based ZLyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.20nMAssay Description:Inhibition of wild type RET (unknown origin) by FRET-based ZLyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetVascular endothelial growth factor receptor 3(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 5.10nMAssay Description:Inhibition of FLT4 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 5.70nMAssay Description:Inhibition of RET G810S mutant (unknown origin) by FRET-based ZLyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 7.10nMAssay Description:Inhibition of RET G810C mutant (unknown origin) by FRET-based ZLyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase receptor Ret(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 8.30nMAssay Description:Inhibition of RET G810R mutant (unknown origin) by FRET-based ZLyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetVascular endothelial growth factor receptor 2(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 27nMAssay Description:Inhibition of KDR (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetVascular endothelial growth factor receptor 1(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 35nMAssay Description:Inhibition of FLT1 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 53nMAssay Description:Inhibition of FLT3 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFibroblast growth factor receptor 1(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 90nMAssay Description:Inhibition of FGFR1 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFibroblast growth factor receptor 4(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 113nMAssay Description:Inhibition of FGFR4 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetEpithelial discoidin domain-containing receptor 1(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 334nMAssay Description:Inhibition of DDR1 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase JAK2(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 2.65E+3nMAssay Description:Inhibition of JAK2 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase Mer(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of MER (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHepatocyte growth factor receptor(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of MET (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetSerine/threonine-protein kinase Nek2(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of NEK2 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetMitogen-activated protein kinase kinase kinase kinase 4(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of NIK (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetMitogen-activated protein kinase kinase kinase kinase 2(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of GCK (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase HCK(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of HCK (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetMast/stem cell growth factor receptor Kit(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of KIT (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetMitogen-activated protein kinase kinase kinase kinase 4(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of MAP4K4 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetPhosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of PI3Ka (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetMacrophage-stimulating protein receptor(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of RON (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProto-oncogene tyrosine-protein kinase ROS(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of ROS1 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHigh affinity nerve growth factor receptor(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of TRKA (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetMacrophage colony-stimulating factor 1 receptor(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of CSF-1R (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetEpidermal growth factor receptor(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of EGFR (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetMitogen-activated protein kinase 3(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of ERK1 (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetFocal adhesion kinase 1(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of FAK (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetAurora kinase A(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of Aurora A (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetAurora kinase B(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of Aurora B (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetProtein-tyrosine kinase 6(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of BRK (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetTyrosine-protein kinase BTK(Human)
Affiliated Hengyang Hospital of Hunan Normal University & Hengyang Central Hospital

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50664122BDBM50664122(CHEMBL6162402)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of BTK (unknown origin) by FRET-based Z-Lyte kinase assayMore data for this Ligand-Target Pair
Ligand Info
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed