BDBM50096708 (E)-2-(3,4-Difluoro-phenyl)-ethenesulfonic acid [4-(4-chloro-phenyl)-5-propyl-thiazol-2-yl]-amide::CHEMBL432801

SMILES CCCc1sc(NS(=O)(=O)\C=C\c2ccc(F)c(F)c2)nc1-c1ccc(Cl)cc1

InChI Key InChIKey=YMTGCYFDOUHFBJ-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50096708   

TargetDual specificity protein phosphatase 3(Human)
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50096708((E)-2-(3,4-Difluoro-phenyl)-ethenesulfonic acid [4...)
Affinity DataIC50: 2.00E+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
LigandPNGBDBM50096708((E)-2-(3,4-Difluoro-phenyl)-ethenesulfonic acid [4...)
Affinity DataIC50: 2.00E+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
LigandPNGBDBM50096708((E)-2-(3,4-Difluoro-phenyl)-ethenesulfonic acid [4...)
Affinity DataIC50: 2.10E+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