null

SMILES COc1ccc(cc1)-c1cc(cc(-c2ccc(OC)cc2)c1OCC(O)=O)-c1ccc(cc1)-c1c(Cc2ccccc2)sc2ccccc12

InChI Key InChIKey=MXPGUEIHEJPIBY-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50086950   

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

Curated by ChEMBL
LigandPNGBDBM50086950(2-[4-[4-(2-benzylbenzo[b]thiophen-3-yl)phenyl]-2,6...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay 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
LigandPNGBDBM50086950(2-[4-[4-(2-benzylbenzo[b]thiophen-3-yl)phenyl]-2,6...)copy SMILEScopy InChI
Affinity DataIC50: 25.1nMAssay 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
LigandPNGBDBM50086950(2-[4-[4-(2-benzylbenzo[b]thiophen-3-yl)phenyl]-2,6...)copy SMILEScopy InChI
Affinity DataIC50: 2.51E+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