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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

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50115731   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Protein-tyrosine phosphatase 1B


(Homo sapiens (Human))
BDBM50115731
PNG
(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Show SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:11|
Show InChI InChI=1S/C18H12O4/c1-22-18(21)12-8-6-11(7-9-12)15-10-16(19)17(20)14-5-3-2-4-13(14)15/h2-10H,1H3
PDB
MMDB

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PC sid
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PubMed
n/an/a 1.54E+3n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against recombinant human protein-tyrosine phosphatase 1B (PTP1B) using fluoreacein diphosphate (FDP) as a substrate


Bioorg Med Chem Lett 12: 1941-6 (2002)


BindingDB Entry DOI: 10.7270/Q2QZ2999
More data for this
Ligand-Target Pair
Leukocyte common antigen


(Homo sapiens (Human))
BDBM50115731
PNG
(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Show SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:11|
Show InChI InChI=1S/C18H12O4/c1-22-18(21)12-8-6-11(7-9-12)15-10-16(19)17(20)14-5-3-2-4-13(14)15/h2-10H,1H3
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PubMed
n/an/a 1.65E+3n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
In vitro inhibitory activity of the compound against recombinant human CD45 using fluoreacein diphosphate (FDP) as a substrate


Bioorg Med Chem Lett 12: 1941-6 (2002)


BindingDB Entry DOI: 10.7270/Q2QZ2999
More data for this
Ligand-Target Pair
Dual specificity phosphatase Cdc25B


(Homo sapiens (Human))
BDBM50115731
PNG
(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Show SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:11|
Show InChI InChI=1S/C18H12O4/c1-22-18(21)12-8-6-11(7-9-12)15-10-16(19)17(20)14-5-3-2-4-13(14)15/h2-10H,1H3
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PubMed
n/an/a 2.13E+3n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
In vitro inhibitory activity of the compound against recombinant human Cdc25B using fluoreacein diphosphate (FDP) as a substrate


Bioorg Med Chem Lett 12: 1941-6 (2002)


BindingDB Entry DOI: 10.7270/Q2QZ2999
More data for this
Ligand-Target Pair
Receptor-type tyrosine-protein phosphatase F (LAR)


(Homo sapiens (Human))
BDBM50115731
PNG
(4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...)
Show SMILES COC(=O)c1ccc(cc1)C1=CC(=O)C(=O)c2ccccc12 |t:11|
Show InChI InChI=1S/C18H12O4/c1-22-18(21)12-8-6-11(7-9-12)15-10-16(19)17(20)14-5-3-2-4-13(14)15/h2-10H,1H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
n/an/a 7.09E+3n/an/an/an/an/an/a



Korea Research Institute of Chemical Technology

Curated by ChEMBL


Assay Description
In vitro inhibitory activity of the compound against recombinant human LAR using fluoreacein diphosphate (FDP) as a substrate


Bioorg Med Chem Lett 12: 1941-6 (2002)


BindingDB Entry DOI: 10.7270/Q2QZ2999
More data for this
Ligand-Target Pair