null

SMILES COc1cc2ncnc(Nc3ccc(-c4nc5ccccc5s4)c(OC)c3)c2cc1OC

InChI Key InChIKey=CBIHKNQEUSGCEN-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50248349   

TargetAurora kinase B(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Aurora B by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed
TargetInsulin receptor(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of insulin receptor by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of IGF1R by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 63nMAssay Description:Inhibition of EGFR by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of VEGFR2 by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed
TargetProto-oncogene tyrosine-protein kinase Src(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Src by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed
TargetAurora kinase A(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of Aurora A by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed
TargetEphrin type-B receptor 4(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50248349(CHEMBL473553 | N-(4-(benzo[d]thiazol-2-yl)-3-metho...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of EphB4 by virtual HTS assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736QS3PubMed