BDBM69369 2-(4-methoxyanilino)benzoic acid::2-(p-anisidino)benzoic acid::2-[(4-methoxyphenyl)amino]benzoic acid::MLS000775662::SMR000370544::cid_202918

SMILES COc1ccc(Nc2ccccc2C(O)=O)cc1

InChI Key InChIKey=AOTGWRVCPVLSPA-UHFFFAOYSA-N

Data  5 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 69369   

TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Broad Institute

Curated by PubChem BioAssay
LigandPNGBDBM69369(2-(4-methoxyanilino)benzoic acid | 2-(p-anisidino)...)
Affinity DataEC50: >3.00E+5nMAssay Description:Keywords: GSK3beta, dose response, kinase, inhibition, HTS Assay Overview: The glycogen synthase kinase-3 beta (GSK-3b) is a known master regulator f...More data for this Ligand-Target Pair
In DepthDetails PCBioAssay
TargetDihydroorotate dehydrogenase (quinone), mitochondrial(Homo sapiens (Human))
Broad Institute

Curated by ChEMBL
LigandPNGBDBM69369(2-(4-methoxyanilino)benzoic acid | 2-(p-anisidino)...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of human recombinant DHODHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProcathepsin L(Homo sapiens (Human))
Universidade Federal De S£O Carlos

Curated by ChEMBL
LigandPNGBDBM69369(2-(4-methoxyanilino)benzoic acid | 2-(p-anisidino)...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of human recombinant cathepsin L expressed in Pichia pastoris using Z-Phe-Arg-MCA as substrate by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM69369(2-(4-methoxyanilino)benzoic acid | 2-(p-anisidino)...)
Affinity DataIC50:  90nMAssay Description:Inhibition of recombinant AKR1C3 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin L2(Homo sapiens (Human))
Universidade Federal De S£O Carlos

Curated by ChEMBL
LigandPNGBDBM69369(2-(4-methoxyanilino)benzoic acid | 2-(p-anisidino)...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of human recombinant cathepsin V expressed in Pichia pastoris using Z-Phe-Arg-MCA as substrate by fluorometric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM69369(2-(4-methoxyanilino)benzoic acid | 2-(p-anisidino)...)
Affinity DataIC50:  700nMAssay Description:Inhibition of recombinant AKR1C2 assessed as NADP+ dependent oxidation of S-tetralol by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed