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Assay Detail

CHEMBL5585351

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

Toxicity
Inhibition of fluorescence tracer red binding to human ERG measured after 3 hrs by fluorescence polarization assay
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Toxicity
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Publication

Design, synthesis, biological evaluation, and in silico studies of novel pyridopyridine derivatives as anticancer candidates targeting FMS kinase.
Sebastian A, Abu Rabah RR, Zaraei SO, Vunnam S, Sultan S, Anbar HS, El-Gamal R, Tarazi H, Sarg N, Alhamad DW, Al Shamma SA, Shahin AI, Omar HA, Al-Tel TH, El-Gamal MI.
Eur J Med Chem (2024) 274 : 116557 -116557
PubMed 38850857 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 5.31 7.83

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL536480 1 7.83
CHEMBL5598552 1 4.08
CHEMBL5598003 1 4.02

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL536480 IC50 = 14.7 nM 7.83
CHEMBL5598552 IC50 = 83450.0 nM 4.08
CHEMBL5598003 IC50 = 95900.0 nM 4.02