null

SMILES COc1ccc2nc(sc2c1)-c1ccc(Nc2ncnc3cc(OCCCN4CCN(C)CC4)c(OC)cc23)cc1

InChI Key InChIKey=MOQBNQNUPNPLCH-UHFFFAOYSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 8 hits for monomerid = 50304212   

TargetVascular endothelial growth factor receptor 3(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of VEGFR3 by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed
TargetAurora kinase B(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 48nMAssay Description:Inhibition of Aurora-B by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed
TargetAurora kinase A(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:Inhibition of Aurora-A by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of wild type EGF-R by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed
TargetAngiopoietin-1 receptor(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 390nMAssay Description:Inhibition of TIE2 by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed
TargetReceptor tyrosine-protein kinase erbB-2(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of ERBB2 by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of PDGFRbeta by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
4SC AG

Curated by ChEMBL
LigandPNGBDBM50304212(CHEMBL593306 | N-[4-(Benzo[d]thiazol-2''-yl)-3-chl...)copy SMILEScopy InChI
Affinity DataIC50: 690nMAssay Description:Inhibition of VEGFR2 by microplate scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FJ2GWCPubMed