BDBM50038412 2-Oxy-4-phenyl-furazan-3-carbonitrile::3-cyano-4-phenyl-1,2,5-oxadiazole 2-oxide::CHEMBL336467::furoxan

SMILES [O-][n+]1onc(c1C#N)-c1ccccc1

InChI Key InChIKey=PMYJGTWUVVVOFO-UHFFFAOYSA-N

Data  4 IC50  2 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 6 hits for monomerid = 50038412   

TargetThioredoxin reductase 1, cytoplasmic(Rattus norvegicus)
National Human Genome Research Institute

Curated by ChEMBL
LigandPNGBDBM50038412(2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...)
Affinity DataIC50: >4.00E+5nMAssay Description:Inhibition of rat recombinant TrxR1 after 10 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMultidrug resistance-associated protein 1(Homo sapiens (Human))
Universita Degli Studi Di Torino

Curated by ChEMBL
LigandPNGBDBM50038412(2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...)
Affinity DataEC50:  4.20E+4nMAssay Description:Inhibition of MRP1 expressed in MDCK cells assessed as calcein AM accumulation by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
Universita Degli Studi Di Torino

Curated by ChEMBL
LigandPNGBDBM50038412(2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...)
Affinity DataEC50: >1.00E+5nMAssay Description:Inhibition of MDR1 expressed in MDCK cells assessed as calcein AM accumulation by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThioredoxin glutathione reductase(Schistosoma mansoni)
National Human Genome Research Institute

Curated by ChEMBL
LigandPNGBDBM50038412(2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...)
Affinity DataIC50:  6.30E+3nMAssay Description:Inhibition of Schistosoma mansoni TGRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione reductase, mitochondrial(Homo sapiens (Human))
National Human Genome Research Institute

Curated by ChEMBL
LigandPNGBDBM50038412(2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of human recombinant GR after 15 mins in presence of NADPHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThioredoxin glutathione reductase(Schistosoma mansoni)
National Human Genome Research Institute

Curated by ChEMBL
LigandPNGBDBM50038412(2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of Schistosoma mansoni recombinant thioredoxin glutathione reductase assessed as 5-thio-2nitrobezoic acid formation after 3 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed