BDBM50326156 8-{2-[4-(Piperidin-1-yl)phenyl]thiazol-4-yl}dibenzo[b,d]furan-4-carboxylic acid::CHEMBL1242553

SMILES OC(=O)c1cccc2c3cc(ccc3oc12)-c1csc(n1)-c1ccc(cc1)N1CCCCC1

InChI Key InChIKey=SWMIHBFCUYUTFG-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50326156   

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

Curated by ChEMBL
LigandPNGBDBM50326156(8-{2-[4-(Piperidin-1-yl)phenyl]thiazol-4-yl}dibenz...)
Affinity DataIC50: 121nMAssay Description:Inhibition of human recombinant PTP1B after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/11/2011
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 2(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326156(8-{2-[4-(Piperidin-1-yl)phenyl]thiazol-4-yl}dibenz...)
Affinity DataIC50: 2.07E+3nMAssay Description:Inhibition of human recombinant TCPTP after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/11/2011
Entry Details Article
PubMed
TargetReceptor-type tyrosine-protein phosphatase F(Human)
Glenmark Research Center

Curated by ChEMBL
LigandPNGBDBM50326156(8-{2-[4-(Piperidin-1-yl)phenyl]thiazol-4-yl}dibenz...)
Affinity DataIC50: 2.07E+3nMAssay Description:Inhibition of human recombinant LAR after 30 mins by spectrophotometryMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/11/2011
Entry Details Article
PubMed