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Assay Detail

CHEMBL4355091

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

Binding
Inhibition of recombinant human IDO1 assessed as reduction in formation of N-formylkynurenine using L-tryptophan as substrate by UV-VIS spectrometric 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

Recent advances in the discovery of indoleamine 2,3-dioxygenase 1 (IDO1) inhibitors.
Wang XX, Sun SY, Dong QQ, Wu XX, Tang W, Xing YQ.
Medchemcomm (2019) 10 : 1740 -1754
PubMed 32055299 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 7.03 7.03

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL51085 EBSELEN 3.0 1 7.03

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL51085 EBSELEN Ki = 94.0 nM 7.03