BDBM50300308 4-Amino-N-(3-chlorophenyl)-1,2,5-oxadiazole-3-carboximidamide::CHEMBL584992

SMILES NC(=Nc1cccc(Cl)c1)c1nonc1N

InChI Key InChIKey=ARPQKQSPFIFUCC-UHFFFAOYSA-N

Data  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 3 hits for monomerid = 50300308   

TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50300308(4-Amino-N-(3-chlorophenyl)-1,2,5-oxadiazole-3-carb...)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibition of IDO1 by magnetic circular dichroism spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50300308(4-Amino-N-(3-chlorophenyl)-1,2,5-oxadiazole-3-carb...)
Affinity DataIC50: >2.00E+3nMAssay Description:Inhibition of indoleamine 2,3-dioxygenase in IFN-gamma-stimulated human HeLa cells assessed as kynurenine formation by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50300308(4-Amino-N-(3-chlorophenyl)-1,2,5-oxadiazole-3-carb...)
Affinity DataIC50: >2.00E+4nMAssay Description:Inhibition of N-terminal his-tagged human indoleamine 2,3-dioxygenase expressed in Escherichia coli assessed as N'-formylkynurenine formation by spec...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed