BDBM50096707 (E)-2-(2-Chloro-phenyl)-ethenesulfonic acid (4,5-diphenyl-thiazol-2-yl)-amide::CHEMBL110566

SMILES Clc1ccccc1\C=C\S(=O)(=O)Nc1nc(c(s1)-c1ccccc1)-c1ccccc1

InChI Key InChIKey=PGKUWFJHCPBEKI-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 = 50096707   

TargetDual specificity protein phosphatase 3(Human)
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50096707((E)-2-(2-Chloro-phenyl)-ethenesulfonic acid (4,5-d...)
Affinity DataIC50: 4.00E+4nMAssay Description:In vitro inhibitory activity against human recombinant VHR phosphatase enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50096707((E)-2-(2-Chloro-phenyl)-ethenesulfonic acid (4,5-d...)
Affinity DataIC50: 3.80E+4nMAssay Description:In vitro inhibitory activity against human recombinant PTP1B phosphatase enzymeMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 2(Human)
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50096707((E)-2-(2-Chloro-phenyl)-ethenesulfonic acid (4,5-d...)
Affinity DataIC50: 2.60E+4nMAssay Description:In vitro inhibitory activity against human recombinant Cell division cycle 25BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed