null

SMILES COC1=CC(=O)C(CC(=O)Cc2ccc(O)c(OC)c2)=C(C1=O)c1cc(CCCc2ccc(O)c(OC)c2)c(OC)cc1O

InChI Key InChIKey=JEXSYRYFKRSWCY-UHFFFAOYSA-N

  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 2 hits for monomerid = 112632   

TargetCystathionine gamma-lyase(Homo sapiens (Human))
Shanghai Center for Systems Biomedicine, School of Pharmacy, and State Key Laboratory of Microbial Metabolism & School of Life Sciences and Biotechnology

LigandPNGBDBM112632(Euonyquinone A (5))copy SMILEScopy InChI
Affinity DataIC50: 2.00E+5nMpH: 7.0 T: 2°CAssay Description:500 nM hCSE in optimal buffer (50 mM Hepes, pH 7.0; final concentration) was incubated with compound for 45 min in the 192-tandem-well plate before a...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75F0FPubMed
TargetDopa decarboxylase (Aromatic L-amino acid decarboxylase), isoform CRA_a(Homo sapiens (Human))
Shanghai Center for Systems Biomedicine, School of Pharmacy, and State Key Laboratory of Microbial Metabolism & School of Life Sciences and Biotechnology

LigandPNGBDBM112632(Euonyquinone A (5))copy SMILEScopy InChI
Affinity DataIC50: 1.15E+4nMpH: 8.05 T: 2°CAssay Description:To the wells of a 384-well polypropylene plate, 1 µL DMSO (control) or test compounds at indicated concentrations were added, followed by the ad...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2S75F0FPubMed