null

SMILES CN1CCN(CCc2ccc(NC(=O)c3cc(c[nH]c3=O)-c3ccc4OCOc4c3)cc2)CC1

InChI Key InChIKey=JNAZGEGXKHNDBG-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50181672   

TargetBreakpoint cluster region protein/Tyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 9.50E+3nMAssay Description:Antiproliferative activity against human BCR-ABL positive chronic myeloid leukemia K562 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 7.50E+3nMAssay Description:Antiproliferative activity against human NPM-ALK positive anaplastic large cell lymphoma karpas299 cell lineMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Inhibitory activity against ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetALK tyrosine kinase receptor/Nucleophosmin(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 1.74E+4nMAssay Description:Antiproliferative activity against murine BaF3 cell line expressing NPM-ALKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibitory activity against IGF1RMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibitory activity against Flt3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against SrcMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory activity against AblMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed
TargetInsulin receptor(Homo sapiens (Human))
ChemBridge Research Laboratories and ChemBridge Corporation

Curated by ChEMBL
LigandPNGBDBM50181672(5-benzo[1,3]dioxol-5-yl-2-oxo-1,2-dihydro-pyridine...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibitory activity against IRKMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H994T6PubMed