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Assay Detail

CHEMBL3756250

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

Binding
Inhibition of IDO1 in IFNgamma-stimulated human HeLa cells incubated for 24 hrs
10
Total Activities
10
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

Important Hydrogen Bond Networks in Indoleamine 2,3-Dioxygenase 1 (IDO1) Inhibitor Design Revealed by Crystal Structures of Imidazoleisoindole Derivatives with IDO1.
Peng YH, Ueng SH, Tseng CT, Hung MS, Song JS, Wu JS, Liao FY, Fan YS, Wu MH, Hsiao WC, Hsueh CC, Lin SY, Cheng CY, Tu CH, Lee LC, Cheng MF, Shia KS, Shih C, Wu SY.
J Med Chem (2016) 59 : 282 -293
PubMed 26642377 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 10 6.69 7.26

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3753837 1 7.26
CHEMBL3629569 1 7.21
CHEMBL3754460 1 6.14
CHEMBL3629570 1 6.13
CHEMBL3752239 1 -
CHEMBL3747548 1 -
CHEMBL3753777 1 -
CHEMBL3752209 1 -
CHEMBL3754016 1 -
CHEMBL3752732 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3753837 EC50 = 55.0 nM 7.26
CHEMBL3629569 EC50 = 61.0 nM 7.21
CHEMBL3754460 EC50 = 725.0 nM 6.14
CHEMBL3629570 EC50 = 749.0 nM 6.13
CHEMBL3752239 EC50 > 10000.0 nM -
CHEMBL3747548 EC50 > 10000.0 nM -
CHEMBL3753777 EC50 > 10000.0 nM -
CHEMBL3752209 EC50 - -
CHEMBL3754016 EC50 - -
CHEMBL3752732 EC50 - -