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Assay Detail

CHEMBL3369563

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

Binding
Binding affinity to human His-tagged PPARgamma LBD by SPR method
12
Total Activities
12
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

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

Publication

Molecular dynamics study-guided identification of cyclic amine structures as novel hydrophobic tail components of hPPARγ agonists.
Tanaka Y, Gamo K, Oyama T, Ohashi M, Waki M, Matsuno K, Matsuura N, Tokiwa H, Miyachi H.
Bioorg Med Chem Lett (2014) 24 : 4001 -4005
PubMed 25017035 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Kd 12 9.29 10.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3317860 1 10.00
CHEMBL3317867 1 9.96
CHEMBL3317863 1 9.40
CHEMBL3317865 1 9.39
CHEMBL3317864 1 9.19
CHEMBL3317866 1 9.10
CHEMBL3317455 1 8.74
CHEMBL3317858 1 8.54
CHEMBL1651239 1 -
CHEMBL3317862 1 -
CHEMBL3317861 1 -
CHEMBL3317859 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3317860 Kd = 0.1 nM 10.00
CHEMBL3317867 Kd = 0.11 nM 9.96
CHEMBL3317863 Kd = 0.4 nM 9.40
CHEMBL3317865 Kd = 0.41 nM 9.39
CHEMBL3317864 Kd = 0.64 nM 9.19
CHEMBL3317866 Kd = 0.8 nM 9.10
CHEMBL3317455 Kd = 1.82 nM 8.74
CHEMBL3317858 Kd = 2.85 nM 8.54
CHEMBL1651239 Kd - -
CHEMBL3317862 Kd - -
CHEMBL3317861 Kd - -
CHEMBL3317859 Kd - -