BDBM48089 (5E)-5-(4-hydroxybenzylidene)-3-(3-pyridyl)-2-thioxo-thiazolidin-4-one::(5E)-5-[(4-hydroxyphenyl)methylidene]-3-(3-pyridinyl)-2-sulfanylidene-4-thiazolidinone::(5E)-5-[(4-hydroxyphenyl)methylidene]-3-pyridin-3-yl-2-sulfanylidene-1,3-thiazolidin-4-one::5-(4-hydroxybenzylidene)-3-(3-pyridinyl)-2-thioxo-1,3-thiazolidin-4-one::MLS000701212::SMR000230559::cid_6115882

SMILES Oc1ccc(\C=C2\SC(=S)N(C2=O)c2cccnc2)cc1

InChI Key InChIKey=QMICZQHBCZSATN-MDWZMJQESA-N

Data  1 IC50  1 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 = 48089   

TargetKappa-type opioid receptor(Homo sapiens (Human))
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM48089((5E)-5-(4-hydroxybenzylidene)-3-(3-pyridyl)-2-thio...)
Affinity DataIC50:  1.14E+4nMAssay 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 DepthDetails PCBioAssay
TargetBeta-galactosidase(Escherichia coli)
Burnham Center For Chemical Genomics

Curated by PubChem BioAssay
LigandPNGBDBM48089((5E)-5-(4-hydroxybenzylidene)-3-(3-pyridyl)-2-thio...)
Affinity DataEC50:  1.47E+4nMAssay 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 DepthDetails PCBioAssay