BDBM50287565 CHEMBL4163084::US11572354, Compound 10c

SMILES Oc1ccccc1-c1cncn1Cc1cc2cc(Br)ccc2[nH]1

InChI Key InChIKey=PIPVVXXXDHECFG-UHFFFAOYSA-N

Data  3 IC50  1 EC50

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50287565   

TargetIndoleamine 2,3-dioxygenase 1(Human)
University Health Network

US Patent
LigandPNGBDBM50287565(CHEMBL4163084 | US11572354, Compound 10c)
Affinity DataIC50: 180nMAssay Description:A standard reaction mixture (200uL/well) containing 50mM potassium phosphate buffer (pH 6.5), 20 mM ascorbic acid (neutralized with NaOH), 200 ug/mL ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/26/2023
Entry Details
US Patent

TargetIndoleamine 2,3-dioxygenase 1(Human)
University Health Network

US Patent
LigandPNGBDBM50287565(CHEMBL4163084 | US11572354, Compound 10c)
Affinity DataIC50: 180nMAssay Description:Inhibition of recombinant human IDO1 assessed as reduction in kynurenine production using L-tryptophan as substrate after 1 hrMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/23/2020
Entry Details Article
PubMed
TargetIndoleamine 2,3-dioxygenase 1(Human)
University Health Network

US Patent
LigandPNGBDBM50287565(CHEMBL4163084 | US11572354, Compound 10c)
Affinity DataEC50:  1.45E+3nMAssay Description:Inhibition of recombinant human IDO1 assessed as reduction in kynurenine production using L-tryptophan as substrate after 1 hrMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/23/2020
Entry Details Article
PubMed
TargetTryptophan 2,3-dioxygenase 2(Human)
University Health Network

US Patent
LigandPNGBDBM50287565(CHEMBL4163084 | US11572354, Compound 10c)
Affinity DataIC50: 1.58E+5nMAssay Description:A Standard reaction mixture (200 uL/well) containing 50 mM potassium phosphate buffer (pH 6.5), 20mM ascorbic acid (neutralized with NaOH), 200 ug/ml...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/26/2023
Entry Details
US Patent