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SMILES Cc1ccc(cc1)-c1nc(cs1)-c1ccc2oc3c(cccc3c2c1)C(O)=O

InChI Key InChIKey=SJDIGYUJVHXLGI-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 = 50326151   

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

Curated by ChEMBL
LigandPNGBDBM50326151(8-(2-Methylthiazol-4-yl)dibenzo[b,d]furan-4-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 515nMAssay Description:Inhibition of human recombinant PTP1B after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7V6SPubMed
TargetReceptor-type tyrosine-protein phosphatase F(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326151(8-(2-Methylthiazol-4-yl)dibenzo[b,d]furan-4-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 1.32E+3nMAssay Description:Inhibition of human recombinant LAR after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7V6SPubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Homo sapiens (Human))
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326151(8-(2-Methylthiazol-4-yl)dibenzo[b,d]furan-4-carbox...)copy SMILEScopy InChI
Affinity DataIC50: 730nMAssay Description:Inhibition of human recombinant TCPTP after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24Q7V6SPubMed