null

SMILES O[C@@H]1Cc2c(O)cc(O)cc2O[C@@H]1c1ccc(O)cc1

InChI Key InChIKey=RSYUFYQTACJFML-UKRRQHHQSA-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 3 hits for monomerid = 50240892   

TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50240892((-)-epiafzelechin | (2R,3R)-2-(4-Hydroxy-phenyl)-c...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of COX1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q27S7PN5PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University of Illinois at Chicago

Curated by ChEMBL
LigandPNGBDBM50240892((-)-epiafzelechin | (2R,3R)-2-(4-Hydroxy-phenyl)-c...)copy SMILEScopy InChI
Affinity DataIC50: 6.97E+4nMAssay Description:Inhibition of COX2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38TGVPubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50240892((-)-epiafzelechin | (2R,3R)-2-(4-Hydroxy-phenyl)-c...)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+3nMAssay Description:Inhibition of COX1More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2J38TGVPubMed