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
Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
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Protein-tyrosine phosphatase 1B (Homo sapiens (Human)) | BDBM50115731 (4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...) | PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 1.54E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 1.65E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...) | PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 2.13E+3 | n/a | n/a | n/a | n/a | n/a | n/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 (4-(3,4-Dioxo-3,4-dihydro-naphthalen-1-yl)-benzoic ...) | PDB MMDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet | CHEMBL PC cid PC sid UniChem Similars | PubMed | n/a | n/a | 7.09E+3 | n/a | n/a | n/a | n/a | n/a | n/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 |