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Assay Detail

CHEMBL3887716

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

Binding
Inhibition Assay: This test was performed by partially modifying the method of Philip et. al. (J. Biomol. Screen. Vol. 11, pp 481-487, 2006). HEK293 cells that stably express human DAAO were suspended in Cellbanker solution at 5×106 cells/ml and cryopreserved at −80° C. At the time of measurement, the cells were centrifuged at 1000 rpm for one min and the Cellbanker solution was removed. The cells were resuspended at 5×106 cells/ml in FAD-containing buffer (50 mM sodium phosphate [pH 7.5], 18 μM FAD, 0.02% CHAPS). A 4% DMSO buffer solution (50 mM sodium phosphate [pH 7.5], 0.02% CHAPS) of the test compound (4 μL) was added to a 384-well black, low volume plate, the cell suspension (4 μL) was added, and the mixture was incubated at room temperature for 15 min. After incubation, a mixed buffer (4 μL) of 150 mM D-alanine, 1.5 U/mL HRP and 240 μM Amplex red was added to the plate, and the mixture was incubated at room temperature for 30 min, and the fluorescence (excitation w
30
Total Activities
30
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

D-amino-acid oxidase (CHEMBL5485)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Dihydroxy aromatic heterocyclic compound
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 30 8.01 8.62

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3900453 1 8.62
CHEMBL2338795 1 8.36
CHEMBL3985690 1 8.34
CHEMBL2338794 1 8.29
CHEMBL3925924 1 8.26
CHEMBL2338797 1 8.22
CHEMBL2338790 1 8.20
CHEMBL2338803 1 8.15
CHEMBL2338800 1 8.14
CHEMBL2338798 1 8.08
CHEMBL3948236 1 8.08
CHEMBL3941866 1 8.06
CHEMBL3965781 1 8.06
CHEMBL3914284 1 8.05
CHEMBL2338789 1 8.01
CHEMBL3964892 1 8.00
CHEMBL2338787 1 7.96
CHEMBL3913880 1 7.96
CHEMBL3889972 1 7.92
CHEMBL3962430 1 7.89
CHEMBL3950593 1 7.89
CHEMBL3899415 1 7.89
CHEMBL2338796 1 7.85
CHEMBL3914258 1 7.85
CHEMBL3904227 1 7.80
CHEMBL3902215 1 7.75
CHEMBL4107441 1 7.75
CHEMBL2338785 1 7.70
CHEMBL3920414 1 7.60
CHEMBL2338801 LUVADAXISTAT 2.0 1 7.57

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3900453 IC50 = 2.4 nM 8.62
CHEMBL2338795 IC50 = 4.4 nM 8.36
CHEMBL3985690 IC50 = 4.6 nM 8.34
CHEMBL2338794 IC50 = 5.1 nM 8.29
CHEMBL3925924 IC50 = 5.5 nM 8.26
CHEMBL2338797 IC50 = 6.0 nM 8.22
CHEMBL2338790 IC50 = 6.3 nM 8.20
CHEMBL2338803 IC50 = 7.0 nM 8.15
CHEMBL2338800 IC50 = 7.2 nM 8.14
CHEMBL2338798 IC50 = 8.3 nM 8.08
CHEMBL3948236 IC50 = 8.4 nM 8.08
CHEMBL3941866 IC50 = 8.8 nM 8.06
CHEMBL3965781 IC50 = 8.8 nM 8.06
CHEMBL3914284 IC50 = 8.9 nM 8.05
CHEMBL2338789 IC50 = 9.8 nM 8.01
CHEMBL3964892 IC50 = 10.0 nM 8.00
CHEMBL2338787 IC50 = 11.0 nM 7.96
CHEMBL3913880 IC50 = 11.0 nM 7.96
CHEMBL3889972 IC50 = 12.0 nM 7.92
CHEMBL3962430 IC50 = 13.0 nM 7.89
CHEMBL3950593 IC50 = 13.0 nM 7.89
CHEMBL3899415 IC50 = 13.0 nM 7.89
CHEMBL2338796 IC50 = 14.0 nM 7.85
CHEMBL3914258 IC50 = 14.0 nM 7.85
CHEMBL3904227 IC50 = 16.0 nM 7.80
CHEMBL3902215 IC50 = 18.0 nM 7.75
CHEMBL4107441 IC50 = 18.0 nM 7.75
CHEMBL2338785 IC50 = 20.0 nM 7.70
CHEMBL3920414 IC50 = 25.0 nM 7.60
CHEMBL2338801 LUVADAXISTAT IC50 = 27.0 nM 7.57