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Assay Detail

CHEMBL5215716

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Binding
Binding affinity to human IDO1 assessed as inhibition constant
2
Total Activities
2
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

X-ray Structure-Guided Discovery of a Potent, Orally Bioavailable, Dual Human Indoleamine/Tryptophan 2,3-Dioxygenase (hIDO/hTDO) Inhibitor That Shows Activity in a Mouse Model of Parkinson's Disease.
Ning XL, Li YZ, Huo C, Deng J, Gao C, Zhu KR, Wang M, Wu YX, Yu JL, Ren YL, Luo ZY, Li G, Chen Y, Wang SY, Peng C, Yang LL, Wang ZY, Wu Y, Qian S, Li GB.
J Med Chem (2021) 64 : 8303 -8332
PubMed 34110158 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 2 6.22 7.72

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3989951 NAVOXIMOD 2.0 1 7.72
CHEMBL571209 INDOXIMOD 2.0 1 4.72

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3989951 NAVOXIMOD Ki = 19.0 nM 7.72
CHEMBL571209 INDOXIMOD Ki = 19000.0 nM 4.72