BDBM50164888 6-Hydroxy-3-[1-(4-hydroxy-phenyl)-meth-(E)-ylidene]-3H-benzofuran-2-one::CHEMBL195416::isoaurostatin

SMILES Oc1ccc(\C=C2\C(=O)Oc3cc(O)ccc23)cc1

InChI Key InChIKey=DJGNNZVFOBIPMK-UHFFFAOYSA-N

Data  21 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 = 50164888   

TargetDNA topoisomerase 2-alpha(Human)
Kumamoto University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50164888BDBM50164888(6-Hydroxy-3-[1-(4-hydroxy-phenyl)-meth-(E)-ylidene...)
Affinity DataIC50: 4.00E+5nMAssay Description:Inhibitory concentration against DNA topoisomerase II activityMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/20/2013
Entry Details Article
PubMed
TargetDNA topoisomerase 2-alpha(Human)
Kumamoto University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50164888BDBM50164888(6-Hydroxy-3-[1-(4-hydroxy-phenyl)-meth-(E)-ylidene...)
Affinity DataIC50: 4.00E+5nMAssay Description:Inhibition human placenta topoisomerase 2 assessed as conversion of catenated kinetoplast DNA to minicircle monomerMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed
TargetDNA topoisomerase 2-alpha(Human)
Kumamoto University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50164888BDBM50164888(6-Hydroxy-3-[1-(4-hydroxy-phenyl)-meth-(E)-ylidene...)
Affinity DataIC50: 4.00E+5nMAssay Description:Inhibition human placenta topoisomerase 2 assessed as conversion of supercoiled pBR322 DNA to relaxed formMore data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed