BDBM50106506 6-Chloro-7-{4-[2-(2-hydroxy-ethoxy)-ethyl]-piperazin-1-yl}-quinoline-5,8-dione::CHEMBL131657

SMILES OCCOCCN1CCN(CC1)C1=C(Cl)C(=O)c2cccnc2C1=O

InChI Key InChIKey=QIBWVZPGFJORRR-UHFFFAOYSA-N

Data  3 IC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50106506   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50106506(6-Chloro-7-{4-[2-(2-hydroxy-ethoxy)-ethyl]-piperaz...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory Activity against Recombinant Human PTP1More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
University of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50106506(6-Chloro-7-{4-[2-(2-hydroxy-ethoxy)-ethyl]-piperaz...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory Activity against Recombinant Human VHRMore 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
LigandPNGBDBM50106506(6-Chloro-7-{4-[2-(2-hydroxy-ethoxy)-ethyl]-piperaz...)
Affinity DataIC50: 900nMAssay Description:Inhibitory activity against recombinant human cell division cycle 25BMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed