null

SMILES Oc1ccc(C=CC(=O)CC(=O)C=Cc2ccc(O)c(O)c2)cc1O

InChI Key InChIKey=OJFGQVZAISEIPG-UHFFFAOYSA-N

  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 4 hits for monomerid = 50067030   

TargetHistone acetyltransferase p300(Homo sapiens (Human))
Università di Roma La Sapienza

Curated by ChEMBL
LigandPNGBDBM50067030((1E,4Z,6E)-1,7-Bis-(3,4-dihydroxy-phenyl)-5-hydrox...)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+4nMAssay Description:Inhibition of GST-p300 HAT assessed as histone acetylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WM1D3KPubMed
TargetIntegrase(Human immunodeficiency virus 1)
Universit£ di Roma"La Sapienza"

Curated by ChEMBL
LigandPNGBDBM50067030((1E,4Z,6E)-1,7-Bis-(3,4-dihydroxy-phenyl)-5-hydrox...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Compound concentration required to reduce HIV-1 Integrase 3'-processing activity by 50%More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29024G3PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Universit£ di Roma"La Sapienza"

Curated by ChEMBL
LigandPNGBDBM50067030((1E,4Z,6E)-1,7-Bis-(3,4-dihydroxy-phenyl)-5-hydrox...)copy SMILEScopy InChI
Affinity DataIC50: 708nMAssay Description:Inhibitory activity against HIV-1 Integrase (HIV-1-IN)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q28W3FGVPubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Yamagata University

Curated by ChEMBL
LigandPNGBDBM50067030((1E,4Z,6E)-1,7-Bis-(3,4-dihydroxy-phenyl)-5-hydrox...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+6nMAssay Description:Inhibition of recombinant BACE1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26T0QMHPubMed