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Assay Detail

CHEMBL761027

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

Binding
Concentration of compound that affords half-maximum transactivation of human Peroxisome proliferator activated receptor gamma in CHO-K1 cells was determined in vitro
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Cell Type CHO-K1
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Peroxisome proliferator-activated receptor gamma (CHEMBL235)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Design, synthesis and evaluation of substituted phenylpropanoic acid derivatives as peroxisome proliferator-activated receptor (PPAR) activators: novel human PPARalpha-selective activators.
Miyachi H, Nomura M, Tanase T, Takahashi Y, Ide T, Tsunoda M, Murakami K, Awano K.
Bioorg Med Chem Lett (2002) 12 : 77 -80
PubMed 11738577 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
EC50 6 5.83 6.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL120009 1 6.40
CHEMBL24458 1 6.10
CHEMBL331206 1 5.60
CHEMBL120744 1 5.55
CHEMBL122009 1 5.52
CHEMBL264374 BEZAFIBRATE 3.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL120009 EC50 = 400.0 nM 6.40
CHEMBL24458 EC50 = 800.0 nM 6.10
CHEMBL331206 EC50 = 2500.0 nM 5.60
CHEMBL120744 EC50 = 2800.0 nM 5.55
CHEMBL122009 EC50 = 3000.0 nM 5.52
CHEMBL264374 BEZAFIBRATE EC50 > 137000.0 nM -