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Assay Detail

CHEMBL5521333

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

Binding
Inhibition of interaction of human PD-1 expressed in Jurkat T cells co-transfected with NFAT/human PD-L1 expressed in CHO-K1 cells co-expressing aAPC preincubated with CHO-K1 cells followed by Jurkat cell addition and measured after 6 hrs by automated microplate spectrophotometer analysis
5
Total Activities
5
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CHO-K1
Confidence 7 — Homologous single protein target
Curated By Autocuration

Publication

Discovery of Novel PD-L1 Small-Molecular Inhibitors with Potent <i>In Vivo</i> Anti-tumor Immune Activity.
Liu L, Zhang H, Hou J, Zhang Y, Wang L, Wang S, Yao Z, Xie T, Wen X, Xu Q, Dai L, Feng Z, Zhang P, Wu Y, Sun H, Liu J, Yuan H.
J Med Chem (2024) 67 : 4977 -4997
PubMed 38465588 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 5 6.63 6.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5562590 1 6.82
CHEMBL5532575 1 6.80
CHEMBL5563757 1 6.45
CHEMBL5092744 1 6.45
CHEMBL5559838 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5562590 EC50 = 152.8 nM 6.82
CHEMBL5532575 EC50 = 158.4 nM 6.80
CHEMBL5563757 EC50 = 353.2 nM 6.45
CHEMBL5092744 EC50 = 356.4 nM 6.45
CHEMBL5559838 EC50 - -