BDBM84506 Acyclic analogue, 12

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

InChI Key InChIKey=FUGACCVMYUBSAM-XIMSKFEESA-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 = 84506   

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

LigandPNGBDBM84506(Acyclic analogue, 12)
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

LigandPNGBDBM84506(Acyclic analogue, 12)
Affinity DataIC50:  9.00E+3nMpH: 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

LigandPNGBDBM84506(Acyclic analogue, 12)
Affinity DataIC50:  1.20E+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 DepthDetails ArticlePubMed