Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL832927

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

Binding
Inhibitory concentration for Glycogen synthase kinase-3 beta was determined in the presence of 10 um ATP (Km 50 uM)
14
Total Activities
14
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

Glycogen synthase kinase-3 beta (CHEMBL262)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Structure-guided design of pyrazolo[1,5-a]pyrimidines as inhibitors of human cyclin-dependent kinase 2.
Williamson DS, Parratt MJ, Bower JF, Moore JD, Richardson CM, Dokurno P, Cansfield AD, Francis GL, Hebdon RJ, Howes R, Jackson PS, Lockie AM, Murray JB, Nunns CL, Powles J, Robertson A, Surgenor AE, Torrance CJ.
Bioorg Med Chem Lett (2005) 15 : 863 -867
PubMed 15686876 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 14 5.06 6.34

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL360573 1 6.34
CHEMBL178785 1 5.47
CHEMBL181114 1 5.40
CHEMBL367150 1 5.29
CHEMBL361833 1 5.28
CHEMBL178769 1 5.06
CHEMBL178268 1 4.92
CHEMBL178179 1 4.66
CHEMBL180814 1 4.55
CHEMBL361348 1 4.40
CHEMBL361231 1 4.30
CHEMBL181293 1 -
CHEMBL180714 1 -
CHEMBL181606 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL360573 IC50 = 460.0 nM 6.34
CHEMBL178785 IC50 = 3400.0 nM 5.47
CHEMBL181114 IC50 = 4000.0 nM 5.40
CHEMBL367150 IC50 = 5100.0 nM 5.29
CHEMBL361833 IC50 = 5300.0 nM 5.28
CHEMBL178769 IC50 = 8700.0 nM 5.06
CHEMBL178268 IC50 = 12000.0 nM 4.92
CHEMBL178179 IC50 = 22000.0 nM 4.66
CHEMBL180814 IC50 = 28000.0 nM 4.55
CHEMBL361348 IC50 = 40000.0 nM 4.40
CHEMBL361231 IC50 = 50000.0 nM 4.30
CHEMBL181293 IC50 > 50000.0 nM -
CHEMBL180714 IC50 > 50000.0 nM -
CHEMBL181606 IC50 > 50000.0 nM -