BDBM50182128 4-nitrobenzo[c][1,2,5]thiadiazole::CHEMBL383084

SMILES [O-][N+](=O)c1cccc2nsnc12

InChI Key InChIKey=IWQKAMJGVIHECB-UHFFFAOYSA-N

Data  2 KI  3 IC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50182128   

TargetThioredoxin reductase(Plasmodium falciparum (isolate 3D7))
University Of Michigan

Curated by ChEMBL
LigandPNGBDBM50182128(4-nitrobenzo[c][1,2,5]thiadiazole | CHEMBL383084)
Affinity DataKi:  650nMAssay Description:Binding affinity to Plasmodium falciparum TrxR in presence of thioredoxinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThioredoxin reductase(Plasmodium falciparum (isolate 3D7))
University Of Michigan

Curated by ChEMBL
LigandPNGBDBM50182128(4-nitrobenzo[c][1,2,5]thiadiazole | CHEMBL383084)
Affinity DataKi:  1.00E+3nMAssay Description:Binding affinity to Plasmodium falciparum TrxR in presence of NADPHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University Of Auckland

Curated by ChEMBL
LigandPNGBDBM50182128(4-nitrobenzo[c][1,2,5]thiadiazole | CHEMBL383084)
Affinity DataIC50:  3.20E+5nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThioredoxin reductase 1, cytoplasmic/2, mitochondrial/3(Homo sapiens (Human))
University Of Michigan

Curated by ChEMBL
LigandPNGBDBM50182128(4-nitrobenzo[c][1,2,5]thiadiazole | CHEMBL383084)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of human TrxRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThioredoxin reductase(Plasmodium falciparum (isolate 3D7))
University Of Michigan

Curated by ChEMBL
LigandPNGBDBM50182128(4-nitrobenzo[c][1,2,5]thiadiazole | CHEMBL383084)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of Plasmodium falciparum TrxRMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed