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Assay Detail

CHEMBL3630804

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

Binding
Inhibition of IDO1 (unknown origin)
11
Total Activities
11
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

Challenges and Opportunities in the Discovery of New Therapeutics Targeting the Kynurenine Pathway.
Dounay AB, Tuttle JB, Verhoest PR.
J Med Chem (2015) 58 : 8762 -8782
PubMed 26207924 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 5.27 7.14
Ki 2 4.68 4.94

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3545369 EPACADOSTAT 3.0 1 7.14
CHEMBL457063 1 5.32
CHEMBL509549 1 5.28
CHEMBL446387 1 5.12
CHEMBL457610 1 5.11
CHEMBL195008 NECROSTATIN 1 4.94
CHEMBL457326 1 4.60
CHEMBL513172 1-METHYLTRYPTOPHAN 1 4.42
CHEMBL14145 1 4.32
CHEMBL444214 1 -
CHEMBL503942 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3545369 EPACADOSTAT IC50 = 72.0 nM 7.14
CHEMBL457063 IC50 = 4800.0 nM 5.32
CHEMBL509549 IC50 = 5300.0 nM 5.28
CHEMBL446387 IC50 = 7600.0 nM 5.12
CHEMBL457610 IC50 = 7700.0 nM 5.11
CHEMBL195008 NECROSTATIN Ki = 11400.0 nM 4.94
CHEMBL457326 IC50 = 25000.0 nM 4.60
CHEMBL513172 1-METHYLTRYPTOPHAN Ki = 38000.0 nM 4.42
CHEMBL14145 IC50 = 48000.0 nM 4.32
CHEMBL444214 IC50 = 365000.0 nM -
CHEMBL503942 IC50 = 1200000.0 nM -