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Assay Detail

CHEMBL3097748

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

Binding
Inhibition of human recombinant DYRK2 expressed in Escherichia coli using GRSRSRSRSRSR as substrate
6
Total Activities
6
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

Publication

Chemical synthesis and biological validation of immobilized protein kinase inhibitory Leucettines.
Burgy G, Tahtouh T, Durieu E, Foll-Josselin B, Limanton E, Meijer L, Carreaux F, Bazureau JP.
Eur J Med Chem (2013) 62 : 728 -737
PubMed 23454515 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 6.79 6.89

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3092863 1 6.89
CHEMBL3092862 1 6.82
CHEMBL1802358 1 6.66
CHEMBL3092864 1 -
CHEMBL3092861 1 -
CHEMBL3092860 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3092863 IC50 = 130.0 nM 6.89
CHEMBL3092862 IC50 = 150.0 nM 6.82
CHEMBL1802358 IC50 = 220.0 nM 6.66
CHEMBL3092864 IC50 > 10000.0 nM -
CHEMBL3092861 IC50 > 10000.0 nM -
CHEMBL3092860 IC50 > 10000.0 nM -