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Assay Detail

CHEMBL3872635

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

Binding
Non-competitive inhibition of recombinant human C-terminal His6-tagged IDO2 (14-420 residues) expressed in Escherichia coli BL21(DE3) in presence of varying concentration of L-tryptophan substrate after 30 mins
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 2 (CHEMBL3627587)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Establishment of a human indoleamine 2, 3-dioxygenase 2 (hIDO2) bioassay system and discovery of tryptanthrin derivatives as potent hIDO2 inhibitors.
Li J, Li Y, Yang D, Hu N, Guo Z, Kuang C, Yang Q.
Eur J Med Chem (2016) 123 : 171 -179
PubMed 27475108 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 1 4.46 4.46

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL312537 1 4.46

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL312537 Ki = 34600.0 nM 4.46