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Assay Detail

CHEMBL4810787

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Binding
Inhibition of IDO1 in human whole blood assessed as unbound concentration
11
Total Activities
8
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Tissue Blood
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Indoleamine 2,3-dioxygenase 1 (CHEMBL4685)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Discovery of IDO1 inhibitors containing a decahydroquinoline, decahydro-1,6-naphthyridine, or octahydro-1H-pyrrolo[3,2-c]pyridine scaffold.
Yu W, Deng Y, Sloman D, Li D, Liu K, Fradera X, Lesburg CA, Martinot T, Doty A, Ferguson H, Richard Miller J, Knemeyer I, Otte K, Vincent S, Sciammetta N, Jonathan Bennett D, Han Y.
Bioorg Med Chem Lett (2021) 49 : 128314 -128314
PubMed 34391891 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 9.44 10.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4863767 1 10.00
CHEMBL4855797 2 9.89
CHEMBL4848630 1 9.54
CHEMBL4848366 2 9.14
CHEMBL4858599 1 9.07
CHEMBL4849622 1 9.01
CHEMBL4853448 1 -
CHEMBL4847151 2 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4863767 IC50 = 0.1 nM 10.00
CHEMBL4855797 IC50 = 0.13 nM 9.89
CHEMBL4848630 IC50 = 0.29 nM 9.54
CHEMBL4848366 IC50 = 0.73 nM 9.14
CHEMBL4858599 IC50 = 0.86 nM 9.07
CHEMBL4849622 IC50 = 0.98 nM 9.01
CHEMBL4855797 IC50 - -
CHEMBL4848366 IC50 - -
CHEMBL4853448 IC50 - -
CHEMBL4847151 IC50 - -
CHEMBL4847151 IC50 - -