BDBM50115731 4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic acid methyl ester::CHEMBL301254

SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12

InChI Key InChIKey=BRCFETUVTSSJSP-UHFFFAOYSA-N

Data  4 IC50

  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 4 hits for monomerid = 50115731   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50115731(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Affinity DataIC50: 1.54E+3nMAssay Description:In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluorescein diphosphate (FDP) as a substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetReceptor-type tyrosine-protein phosphatase C(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50115731(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Affinity DataIC50: 1.65E+3nMAssay Description:In vitro inhibitory activity against recombinant human CD45 using fluorescein diphosphate (FDP) as a substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50115731(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Affinity DataIC50: 2.13E+3nMAssay Description:In vitro inhibitory activity against recombinant human Cdc25B using fluorescein diphosphate (FDP) as a substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetReceptor-type tyrosine-protein phosphatase F(Human)
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50115731(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Affinity DataIC50: 7.09E+3nMAssay Description:In vitro inhibitory activity against recombinant human LAR using fluorescein diphosphate (FDP) as a substrateMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed