BDBM50126145 CHEMBL3629570

SMILES O=C(CC1c2ccccc2-c2cncn12)C1CCCCC1

InChI Key InChIKey=HSQQWDUUFGXQKN-UHFFFAOYSA-N

Data  4 IC50  1 EC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50126145   

TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Colorado College

Curated by ChEMBL
LigandPNGBDBM50126145(CHEMBL3629570)
Affinity DataIC50: <1.00E+3nMAssay Description:Inhibition of human IDO1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Colorado College

Curated by ChEMBL
LigandPNGBDBM50126145(CHEMBL3629570)
Affinity DataIC50: <1.00E+3nMAssay Description:Inhibition of TDO (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Colorado College

Curated by ChEMBL
LigandPNGBDBM50126145(CHEMBL3629570)
Affinity DataIC50:  468nMAssay Description:Inhibition of IDO1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Colorado College

Curated by ChEMBL
LigandPNGBDBM50126145(CHEMBL3629570)
Affinity DataEC50:  749nMAssay Description:Inhibition of IDO1 in IFNgamma-stimulated human HeLa cells incubated for 24 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Colorado College

Curated by ChEMBL
LigandPNGBDBM50126145(CHEMBL3629570)
Affinity DataIC50:  468nMAssay Description:Inhibition of recombinant human IDO1 assessed as conversion of N-formylkynurenine to kynurenine incubated for 1 hr by fluorescence analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed