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Assay Detail

CHEMBL5729995

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

Binding
Inhibition Assay: The inhibitory activity measurement against the kinases mentioned above was measured in the kinase inhibition reaction mixture containing 2 ul purified kinase protein (10-50 ng), 20 mM Tris-HCl, pH 8.0, 5 mM MgCl2, 0.5 mM dithiothreitol, 0.01 mM ATP, 4 ug of poly(D4Y)n peptide substrate (Promega), 0.2 uCi of 32P-ATP and the each compound shown in tablel. The mixture was incubated for 15 min at 30° C. and the reaction was then ended by adding a half volume of 30% phosphoric acid solution. Subsequently, the reaction mixture solution was spotted in avidin coated membrane (Promega). This membrane was washed using 50 mM phosphate, 0.1N NaCl buffer (pH 6.0) solution for 10 min 5 times and then the radioactivity of each spot was quantified by using a BAS image analyzer (Fuji).
3
Total Activities
1
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Ephrin type-A receptor 3 (CHEMBL4954)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Anti-inflammatory compound having inhibitory activity against multiple tyrosine kinases and pharmaceutical composition containing same
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 1 8.29 8.29
kon 1 - -
k_off 1 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2336005 3 8.29

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2336005 IC50 = 5.1 nM 8.29
CHEMBL2336005 kon = - -
CHEMBL2336005 k_off = - s-1 -