BDBM50248085 CHEMBL460746::N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamothioyl)-4-nitrobenzamide

SMILES Oc1ccc(NC(=S)NC(=O)c2ccc(cc2)[N+]([O-])=O)cc1-c1nc2ccccc2s1

InChI Key InChIKey=FRHDZWLQTMKUPC-UHFFFAOYSA-N

Data  11 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 11 hits for monomerid = 50248085   

LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of VEGFR3 by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetInsulin receptor(Human)
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 900nMAssay Description:Inhibition of insulin receptor by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PDGFRbeta by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetFocal adhesion kinase 1(Human)
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 900nMAssay Description:Inhibition of FAK by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetAngiopoietin-1 receptor(Human)
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of TIE2 by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of VEGFR2 by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetCyclin-dependent kinase 2(Human)
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 700nMAssay Description:Inhibition of CDK2 by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetEphrin type-B receptor 4(Human)
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 610nMAssay Description:Inhibition of EphB4 by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 310nMAssay Description:Inhibition of IGF1R by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetEpidermal growth factor receptor(Human)
4Sc

Curated by ChEMBL
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 280nMAssay Description:Inhibition of EGFR by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
LigandPNGBDBM50248085(N-(3-(benzo[d]thiazol-2-yl)-4-hydroxyphenylcarbamo...)
Affinity DataIC50: 190nMAssay Description:Inhibition of Src by virtual HTS assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed