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Assay Detail

CHEMBL4036033

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

Binding
Inhibition of IDO1 in IFN-gamma stimulated human HeLa cells using L-tryptophan as substrate after 24 hrs
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HeLa
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Indoleamine 2,3-dioxygenase 1 (CHEMBL4685)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Identification and preliminary structure-activity relationships of 1-Indanone derivatives as novel indoleamine-2,3-dioxygenase 1 (IDO1) inhibitors.
Gao D, Li Y.
Bioorg Med Chem (2017) 25 : 3780 -3791
PubMed 28526475 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 7 4.90 5.04

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4079351 1 5.04
CHEMBL4062551 1 5.01
CHEMBL4072215 1 4.90
CHEMBL4101667 1 4.88
CHEMBL4063611 1 4.82
CHEMBL4074982 1 4.76
CHEMBL571209 INDOXIMOD 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4079351 EC50 = 9171.0 nM 5.04
CHEMBL4062551 EC50 = 9703.0 nM 5.01
CHEMBL4072215 EC50 = 12520.0 nM 4.90
CHEMBL4101667 EC50 = 13260.0 nM 4.88
CHEMBL4063611 EC50 = 15310.0 nM 4.82
CHEMBL4074982 EC50 = 17540.0 nM 4.76
CHEMBL571209 INDOXIMOD EC50 = 110000.0 nM -