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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Indoleamine 2,3-dioxygenase 1' and Ligand = 'BDBM50509635'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Indoleamine 2,3-dioxygenase 1


(Homo sapiens (Human))
BDBM50509635
PNG
(CHEMBL4465837)
Show SMILES NS(=O)(=O)CC(=O)NCCSc1nonc1\C(Nc1ccc(F)c(c1)C#N)=N\O
Show InChI InChI=1S/C14H14FN7O5S2/c15-10-2-1-9(5-8(10)6-16)19-13(20-24)12-14(22-27-21-12)28-4-3-18-11(23)7-29(17,25)26/h1-2,5,24H,3-4,7H2,(H,18,23)(H,19,20)(H2,17,25,26)
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PC cid
PC sid
UniChem
Article
PubMed
n/an/a 39n/an/an/an/an/an/a



Phenex Pharmaceuticals AG

Curated by ChEMBL


Assay Description
Inhibition of IDO1 in interferon-gamma-induced human SKOV3 cells assessed as N-formylkynurenine formation using L-tryptophan as substrate measured af...


ACS Med Chem Lett 11: 179-187 (2020)


Article DOI: 10.1021/acsmedchemlett.9b00572
BindingDB Entry DOI: 10.7270/Q2GX4FWT
More data for this
Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1


(Homo sapiens (Human))
BDBM50509635
PNG
(CHEMBL4465837)
Show SMILES NS(=O)(=O)CC(=O)NCCSc1nonc1\C(Nc1ccc(F)c(c1)C#N)=N\O
Show InChI InChI=1S/C14H14FN7O5S2/c15-10-2-1-9(5-8(10)6-16)19-13(20-24)12-14(22-27-21-12)28-4-3-18-11(23)7-29(17,25)26/h1-2,5,24H,3-4,7H2,(H,18,23)(H,19,20)(H2,17,25,26)
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 150n/an/an/an/an/an/a



Phenex Pharmaceuticals AG

Curated by ChEMBL


Assay Description
Inhibition of human N-terminal GST-tagged IDO1 expressed in Escherichia coli Rosetta(DE3) pLysS using L-tryptophan as substrate measured after 1 hr b...


ACS Med Chem Lett 11: 179-187 (2020)


Article DOI: 10.1021/acsmedchemlett.9b00572
BindingDB Entry DOI: 10.7270/Q2GX4FWT
More data for this
Ligand-Target Pair