BDBM84505 Acyclic analogue, 11

SMILES COC1=CC(=NC1=Cc1ccc(CCCCC=C)[nH]1)c1ccc([nH]1)C(=O)CCC=C

InChI Key InChIKey=GDSKYCIHLWZEPI-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 = 84505   

TargetTyrosine-protein phosphatase non-receptor type 1(Human)
Max-Planck-Institut FÜR Kohlenforschung

LigandPNGBDBM84505(Acyclic analogue, 11)
Affinity DataIC50: 3.20E+4nMpH: 7.2 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetDual specificity protein phosphatase 3(Human)
Max-Planck-Institut FÜR Kohlenforschung

LigandPNGBDBM84505(Acyclic analogue, 11)
Affinity DataIC50: 5.00E+4nMpH: 6.5 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed
TargetM-phase inducer phosphatase 1(Human)
Max-Planck-Institut FÜR Kohlenforschung

LigandPNGBDBM84505(Acyclic analogue, 11)
Affinity DataIC50: 5.00E+4nMpH: 8.0 T: 2°CAssay Description:Enzyme concentrations were chose to yield absorption changes of 0.2 OD at 405 nm within 80 min for 4-nitrophenyl phosphate (pNPP) in the absence of i...More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/16/2012
Entry Details Article
PubMed