BDBM84504 Acyclic analogue, 10

SMILES COC1=CC(=N\C1=C/c1ccc(CCCCC=C)[nH]1)c1ccc(CCCC=C)[nH]1

InChI Key InChIKey=DXRIGSOKHFFAEB-SWBQMFLXSA-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 = 84504   

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

LigandPNGBDBM84504(Acyclic analogue, 10)
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

LigandPNGBDBM84504(Acyclic analogue, 10)
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

LigandPNGBDBM84504(Acyclic analogue, 10)
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