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Assay Detail

CHEMBL4050282

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

Binding
Inhibition of CK2alpha (unknown origin) (1 to 335 residues) using 5-TAMRA-RADDSDDDDD as substrate after 30 mins by fluorescence imaging method
3
Total Activities
3
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

Casein kinase II subunit alpha (CHEMBL3629)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Oligo-aspartic acid conjugates with benzo[c][2,6]naphthyridine-8-carboxylic acid scaffold as picomolar inhibitors of CK2.
Vahter J, Viht K, Uri A, Enkvist E.
Bioorg Med Chem (2017) 25 : 2277 -2284
PubMed 28274673 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 7.54 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4077554 1 8.40
CHEMBL1230165 SILMITASERTIB 2.0 1 7.70
CHEMBL4067866 1 6.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4077554 IC50 = 4.0 nM 8.40
CHEMBL1230165 SILMITASERTIB IC50 = 20.0 nM 7.70
CHEMBL4067866 IC50 = 300.0 nM 6.52