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Assay Detail

CHEMBL3867378

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

Binding
Inhibition of N-terminus 6xHis-tagged human IDO1 expressed in Escherichia coli M15 using L-tryptophan as substrate preincubated for 1 hr measured after 15 mins in presence of bovine liver and methylene blue by HPLC analysis
14
Total Activities
14
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

Fused Heterocyclic Compounds as Potent Indoleamine-2,3-dioxygenase 1 Inhibitors.
Panda S, Roy A, Deka SJ, Trivedi V, Manna D.
ACS Med Chem Lett (2016) 7 : 1167 -1172
PubMed 27994758 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 7.11 7.11

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3909480 1 7.11
CHEMBL3913975 1 7.11
CHEMBL3971895 1 7.11
CHEMBL3971417 1 7.11
CHEMBL3930308 1 7.11
CHEMBL3940383 1 7.11
CHEMBL3913434 1 7.11
CHEMBL3945146 1 7.11
CHEMBL3974564 1 7.11
CHEMBL3936225 1 7.11
CHEMBL3966057 1 7.11
CHEMBL3927265 1 7.11
CHEMBL584991 1 7.11
CHEMBL504816 (L)-1-METHYLTRYPTOPHAN 1 7.11

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3909480 IC50 = 78.0 nM 7.11
CHEMBL3913975 IC50 = 78.0 nM 7.11
CHEMBL3971895 IC50 = 78.0 nM 7.11
CHEMBL3971417 IC50 = 78.0 nM 7.11
CHEMBL3930308 IC50 = 78.0 nM 7.11
CHEMBL3940383 IC50 = 78.0 nM 7.11
CHEMBL3913434 IC50 = 78.0 nM 7.11
CHEMBL3945146 IC50 = 78.0 nM 7.11
CHEMBL3974564 IC50 = 78.0 nM 7.11
CHEMBL3936225 IC50 = 78.0 nM 7.11
CHEMBL3966057 IC50 = 78.0 nM 7.11
CHEMBL3927265 IC50 = 78.0 nM 7.11
CHEMBL584991 IC50 = 78.0 nM 7.11
CHEMBL504816 (L)-1-METHYLTRYPTOPHAN IC50 = 78.0 nM 7.11