BDBM84511 Acyclic analogue, 16

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

InChI Key InChIKey=HVEJKGZVUHFRID-UVTDQMKNSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 84511   

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

LigandPNGBDBM84511(Acyclic analogue, 16)
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

LigandPNGBDBM84511(Acyclic analogue, 16)
Affinity DataIC50:  8.00E+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

LigandPNGBDBM84511(Acyclic analogue, 16)
Affinity DataIC50:  4.60E+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