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Assay Detail

CHEMBL5386790

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

Binding
Inhibition of GSK3beta (unknown origin) incubated for 20 mins in presence of 33P-ATP
10
Total Activities
10
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

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

Publication

Novel 1,4,5,6-tetrahydrocyclopenta[d]imidazole-5-carboxamide-based JNK3 inhibitors: Design, synthesis, molecular docking, and therapeutic potential in neurodegenerative diseases.
Jun J, Baek J, Kang D, Moon H, Kim H, Cho H, Hah JM.
Eur J Med Chem (2023) 245 : 114917 -114917
PubMed 36395646 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 6.14 8.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL388978 STAUROSPORINE 1 8.39
CHEMBL5411160 1 6.71
CHEMBL5398642 1 6.33
CHEMBL5401511 1 5.90
CHEMBL5424946 1 5.78
CHEMBL5423620 1 5.75
CHEMBL5436023 1 5.65
CHEMBL5403678 1 5.41
CHEMBL5429577 1 5.31
CHEMBL5408675 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL388978 STAUROSPORINE IC50 = 4.106 nM 8.39
CHEMBL5411160 IC50 = 194.8 nM 6.71
CHEMBL5398642 IC50 = 470.0 nM 6.33
CHEMBL5401511 IC50 = 1249.5 nM 5.90
CHEMBL5424946 IC50 = 1659.7 nM 5.78
CHEMBL5423620 IC50 = 1800.1 nM 5.75
CHEMBL5436023 IC50 = 2248.0 nM 5.65
CHEMBL5403678 IC50 = 3889.7 nM 5.41
CHEMBL5429577 IC50 = 4861.0 nM 5.31
CHEMBL5408675 IC50 > 10000.0 nM -