BDBM50300297 4-Amino-N-(4-chlorophenyl)-N'-hydroxy-1,2,5-oxadiazole-3-carboximidamide::CHEMBL573686

SMILES Nc1nonc1C(NO)=Nc1ccc(Cl)cc1

InChI Key InChIKey=SOFDQJMABCOFNN-UHFFFAOYSA-N

Data  3 IC50

  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 3 hits for monomerid = 50300297   

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

Curated by ChEMBL
LigandPNGBDBM50300297(4-Amino-N-(4-chlorophenyl)-N'-hydroxy-1,2,5-oxadia...)
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of IDO1 by magnetic circular dichroism spectroscopic analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/22/2012
Entry Details Article
PubMed
TargetIndoleamine 2,3-dioxygenase 1(Human)
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50300297(4-Amino-N-(4-chlorophenyl)-N'-hydroxy-1,2,5-oxadia...)
Affinity DataIC50: 6.00E+3nMAssay 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 Depth
Date in BDB:
12/26/2012
Entry Details Article
PubMed
TargetIndoleamine 2,3-dioxygenase 1(Human)
Macquarie University

Curated by ChEMBL
LigandPNGBDBM50300297(4-Amino-N-(4-chlorophenyl)-N'-hydroxy-1,2,5-oxadia...)
Affinity DataIC50: 2.40E+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 Depth
Date in BDB:
12/26/2012
Entry Details Article
PubMed