BDBM50326159 8-[2-(4-Carboxyphenyl)thiazol-4-yl]dibenzo[b,d]furan-4-carboxylic acid::CHEMBL1242735

SMILES OC(=O)c1ccc(cc1)-c1nc(cs1)-c1ccc2oc3c(cccc3c2c1)C(O)=O

InChI Key InChIKey=OLLCUWXYFSWOKO-UHFFFAOYSA-N

Data  3 IC50

  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 = 50326159   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326159(8-[2-(4-Carboxyphenyl)thiazol-4-yl]dibenzo[b,d]fur...)
Affinity DataIC50: 388nMAssay Description:Inhibition of human recombinant PTP1B after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326159(8-[2-(4-Carboxyphenyl)thiazol-4-yl]dibenzo[b,d]fur...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of human recombinant TCPTP after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetReceptor-type tyrosine-protein phosphatase F(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326159(8-[2-(4-Carboxyphenyl)thiazol-4-yl]dibenzo[b,d]fur...)
Affinity DataIC50: 3.25E+3nMAssay Description:Inhibition of human recombinant LAR after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed