Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5216253

Review assay metadata, readout intent, target linkage, and publication context from the same page.

Binding
Inhibition of IDO1 (unknown origin)
12
Total Activities
12
Compounds Tested
2
Activity Types
0
Assay Parameters

Assay Information

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

Target

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

Publication

Dual-target inhibitors of indoleamine 2, 3 dioxygenase 1 (Ido1): A promising direction in cancer immunotherapy.
Zhang Y, Hu Z, Zhang J, Ren C, Wang Y.
Eur J Med Chem (2022) 238 : 114524 -114524
PubMed 35696861 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 6.61 9.92
Ki 1 7.55 7.55

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4086143 PF-06840003 1.0 1 9.92
CHEMBL4787695 1 8.30
CHEMBL4756155 1 7.89
CHEMBL3989951 NAVOXIMOD 2.0 1 7.55
CHEMBL3545369 EPACADOSTAT 3.0 1 7.14
CHEMBL4300931 1 7.00
CHEMBL4763910 1 5.93
CHEMBL4749277 1 5.50
CHEMBL4790494 1 5.08
CHEMBL5219208 1 4.85
CHEMBL4749687 1 4.45
CHEMBL5220249 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4086143 PF-06840003 IC50 = 0.12 nM 9.92
CHEMBL4787695 IC50 = 5.0 nM 8.30
CHEMBL4756155 IC50 = 13.0 nM 7.89
CHEMBL3989951 NAVOXIMOD Ki = 28.0 nM 7.55
CHEMBL3545369 EPACADOSTAT IC50 = 73.0 nM 7.14
CHEMBL4300931 IC50 = 100.0 nM 7.00
CHEMBL4763910 IC50 = 1170.0 nM 5.93
CHEMBL4749277 IC50 = 3180.0 nM 5.50
CHEMBL4790494 IC50 = 8400.0 nM 5.08
CHEMBL5219208 IC50 = 14000.0 nM 4.85
CHEMBL4749687 IC50 = 35600.0 nM 4.45
CHEMBL5220249 IC50 = 227000.0 nM -