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Assay Detail

CHEMBL709400

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

Functional
Inhibition of glycogen synthesis in rat skeletal muscle L6 cells
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Rattus norvegicus
Cell Type L6
Confidence 4 — Cell-line / Tissue
Curated By Autocuration

Target

Glycogen synthase kinase-3 (CHEMBL2095188)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

Novel GSK-3 inhibitors with improved cellular activity.
Peat AJ, Garrido D, Boucheron JA, Schweiker SL, Dickerson SH, Wilson JR, Wang TY, Thomson SA.
Bioorg Med Chem Lett (2004) 14 : 2127 -2130
PubMed 15080993 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 10 6.16 6.96

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL65944 1 6.96
CHEMBL306865 GW784752X 1 6.66
CHEMBL66860 1 6.64
CHEMBL69687 1 6.62
CHEMBL66292 PYRAZOLOPYRIMIDINE 2 1 6.51
CHEMBL63727 1 5.91
CHEMBL65988 1 5.73
CHEMBL304533 PYRAZOLOPYRIMIDINE 1 1 5.63
CHEMBL66072 1 5.56
CHEMBL67374 1 5.40

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL65944 EC50 = 110.0 nM 6.96
CHEMBL306865 GW784752X EC50 = 220.0 nM 6.66
CHEMBL66860 EC50 = 230.0 nM 6.64
CHEMBL69687 EC50 = 240.0 nM 6.62
CHEMBL66292 PYRAZOLOPYRIMIDINE 2 EC50 = 310.0 nM 6.51
CHEMBL63727 EC50 = 1220.0 nM 5.91
CHEMBL65988 EC50 = 1880.0 nM 5.73
CHEMBL304533 PYRAZOLOPYRIMIDINE 1 EC50 = 2330.0 nM 5.63
CHEMBL66072 EC50 = 2730.0 nM 5.56
CHEMBL67374 EC50 = 4000.0 nM 5.40