BDBM84510 Acyclic analogue, 17

SMILES CCc1ccc(\C=C2/NC(=O)C=C2OC)[nH]1

InChI Key InChIKey=GXKBJPISIZIVGA-POHAHGRESA-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 = 84510   

TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
Max-Planck-Institut FÜR Kohlenforschung

LigandPNGBDBM84510(Acyclic analogue, 17)
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 DepthDetails ArticlePubMed
TargetDual specificity protein phosphatase 3(Homo sapiens (Human))
Max-Planck-Institut FÜR Kohlenforschung

LigandPNGBDBM84510(Acyclic analogue, 17)
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 DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Max-Planck-Institut FÜR Kohlenforschung

LigandPNGBDBM84510(Acyclic analogue, 17)
Affinity DataIC50: >5.00E+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 DepthDetails ArticlePubMed