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Assay Detail

CHEMBL5216266

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

Binding
Inhibition of human recombinant N-terminal His tagged IDO1 expressed in Escherichia coli using L-Trp as substrate by measuring amount of N-formylkynurenine formed by UV based method
1
Total Activities
1
Compounds Tested
1
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 1 4.03 4.03

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4791168 1 4.03

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4791168 IC50 = 94500.0 nM 4.03