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Assay Detail

CHEMBL3887659

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

Binding
AlphaScreen Assay: The compounds of the present invention can be evaluated by using an aggrecanase ADAMTS-4 and ADAMTS-5 AlphaScreen assay (Miller J. A., et al. Anal. Biochem. 2003, 314, 260-265), with the following modifications: Typically 3 or 4 nM ADAMTS-4 or 2.1 nM ADAMTS-5 is incubated with 80 nM 43-mer peptide substrate+/- inhibitors (1% final DMSO concentration) for 3 hours at room temperature in a white non-binding surface 96 well plate (Corning 3990). Inhibitors are serially diluted 3-fold and tested at final starting concentrations of up to approximately 100 uM. The assay is then quenched with a cocktail containing EDTA (62.5 mM), 50 mM Tris(hydroxymethyl)aminomethane (Tris), (pH 7.5), 10 mM calcium chloride, 100 mM sodium chloride, 0.2% Brij 35 (main component of polyoxyethylene (23) lauryl ether), 0.1% Bovine Serum Albumin (BSA), BC3 monoclonal antibody hybridoma supernatant (1:2000 final dilution), streptavidin conjugated donor beads and anti-mouse IgG conjugated acceptor beads.
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

ADAM metallopeptidase with thrombospondin type 1 motif 4 (CHEMBL3988592)
Type SINGLE PROTEIN
Organism Canis lupus familiaris

Publication

Aggrecanase inhibitors
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 8.90 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4066965 1 9.00
CHEMBL4072836 1 9.00
CHEMBL3980860 1 8.70

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4066965 IC50 = 1.0 nM 9.00
CHEMBL4072836 IC50 = 1.0 nM 9.00
CHEMBL3980860 IC50 = 2.0 nM 8.70