BDBM57115 (5Z)-2-oxidanylidene-4-phenyl-5-(phenylmethylidene)furan-3-carbonitrile::(5Z)-2-oxo-4-phenyl-5-(phenylmethylene)-3-furancarbonitrile::(5Z)-5-benzal-2-keto-4-phenyl-3-furonitrile::(5Z)-5-benzylidene-2-oxo-4-phenylfuran-3-carbonitrile::2-oxo-4-phenyl-5-(phenylmethylene)-2,5-dihydro-3-furancarbonitrile::MLS000539493::SMR000125151::cid_5919900

SMILES O=C1O\C(=C/c2ccccc2)C(=C1C#N)c1ccccc1

InChI Key InChIKey=PEODVUVNVGIRIB-UHFFFAOYSA-N

Data  2 EC50

  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 = 57115   

TargetStreptokinase A(Streptococcus pyogenes M1 GAS)
Broad Institute

Curated by PubChem BioAssay
LigandPNGBDBM57115(MLS000539493 | (5Z)-2-oxidanylidene-4-phenyl-5-(ph...)
Affinity DataEC50:  2.38E+3nMAssay Description:Keywords: Group A streptococcus, GAS, streptokinase, expression, virulence, inhibition, dose response, EC50 Assay Overview: The goal of this assa...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/8/2011
Entry Details
PCBioAssay
TargetNeurotensin receptor type 1(Human)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM57115(MLS000539493 | (5Z)-2-oxidanylidene-4-phenyl-5-(ph...)
Affinity DataEC50:  6.66E+3nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/3/2011
Entry Details
PCBioAssay