null

SMILES COc1ccc(cc1)-c1cc(cc(Br)c1OCC(O)=O)-c1ccc(cc1)-c1c(Cc2ccccc2)sc2ccccc12

InChI Key InChIKey=PEGJJUMNONDEID-UHFFFAOYSA-N

  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 3 hits for monomerid = 50086954   

TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50086954(CHEMBL278092 | [4-(2-Benzyl-benzo[b]thiophen-3-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:In vitro inhibitory activity against human recombinant protein tyrosine phosphatase 1b (PTP1B)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2W958FTPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50086954(CHEMBL278092 | [4-(2-Benzyl-benzo[b]thiophen-3-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 28.8nMAssay Description:Binding affinity to human recombinant PTP1BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27D2WCCPubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50086954(CHEMBL278092 | [4-(2-Benzyl-benzo[b]thiophen-3-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 2.88E+7nMAssay Description:Concentration required for 50% inhibition of tyrosine phosphatase 1BMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2416Z8NPubMed