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Assay Detail

CHEMBL2330526

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

Binding
Inhibition of human recombinant N-terminus 6X-histidine-tagged indoleamine 2,3-dioxygenase expressed in Escherichia coli assessed as inhibition of L-tryptophan to N-formylkynurenine formation measured as residual enzyme activity incubated for 15 mins prior to substrate addition measured after 30 mins by UV-vis spectrophotometric analysis relative to DMSO-treated control
3
Total Activities
2
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

Aminophenoxazinones as inhibitors of indoleamine 2,3-dioxygenase (IDO). Synthesis of exfoliazone and chandrananimycin A.
Pasceri R, Siegel D, Ross D, Moody CJ.
J Med Chem (2013) 56 : 3310 -3317
PubMed 23521768 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 2 5.25 6.34
Ki 1 6.49 6.49

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2322655 CINNABARINIC ACID 2 6.49
CHEMBL14145 1 4.15

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2322655 CINNABARINIC ACID Ki = 326.0 nM 6.49
CHEMBL2322655 CINNABARINIC ACID IC50 = 460.0 nM 6.34
CHEMBL14145 IC50 = 70300.0 nM 4.15