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Assay Detail

CHEMBL4739633

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

Binding
Antagonist activity at human C-terminal His-tagged PD-L1 (18 to 239 residues)/human C-terminal IgG epitope-tagged PD1 (25 to 167 residues) expressed in HEK293 cells incubated for 15 mins by HTRF assay
1
Total Activities
1
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293
Confidence 7 — Homologous single protein target
Curated By Autocuration

Publication

Design, Synthesis, and Biological Evaluation of Imidazopyridines as PD-1/PD-L1 Antagonists.
Butera R,Ważyńska M,Magiera-Mularz K,Plewka J,Musielak B,Surmiak E,Sala D,Kitel R,de Bruyn M,Nijman HW,Elsinga PH,Holak TA,Dömling A
ACS Med Chem Lett (2021) 12 : 768 -773
PubMed 34055224 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.65 8.65

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4084368 1 8.65

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4084368 IC50 = 2.25 nM 8.65