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Assay Detail

CHEMBL3887109

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

Binding
Inhibition Assay: Recombinant BACE-2 (extracellular domain, expressed in baculovirus and purified using standard methods) at 0.1 to 1 nM concentrations is incubated with the test compound at various concentrations for 1 hour at room temperature in 100 mM acetate buffer, pH 4.5, containing 0.1% CHAPS. Activity was measured using a final concentration of 3 μM of the fluorescence-quenched substrate Q-C(HSO3)-Ile-Asp-Leu-Ala-Val-Leu-Asp-HN-CH2-CH2-Mca, where Q=2-nitro-5-amino benzoic acid and Mca=7-methoxy-4-coumarinyl acetic acid. Catalytic turnover was monitored in a Spectramax Gemini fluorescence plate reader (Molecular Devices) in black 96-well microplates using excitation/emission wavelength of 325 nm and 400 nm, respectively. Fluorescence increase was followed for 15 min, in 1 minute's intervals. The fluorescence/time slopes were calculated from duplicate wells and from wells without inhibitor and the IC50 values were calculated using a logistic 4-parameter model.
35
Total Activities
35
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Beta-secretase 2 (CHEMBL2525)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Oxazine derivatives and their use in the treatment of disease
(2015)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 35 6.36 8.40

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2386724 1 8.40
CHEMBL2386726 1 8.15
CHEMBL4111699 1 7.57
CHEMBL4115329 1 7.32
CHEMBL4114267 1 7.18
CHEMBL2386720 1 7.15
CHEMBL4111654 1 7.03
CHEMBL4106556 1 7.02
CHEMBL4109969 1 6.92
CHEMBL2386721 1 6.85
CHEMBL4112589 1 6.58
CHEMBL2386719 1 6.58
CHEMBL2386723 1 6.54
CHEMBL4109860 1 6.38
CHEMBL4110655 1 6.31
CHEMBL2386722 1 6.24
CHEMBL4112705 1 6.24
CHEMBL4110172 1 6.14
CHEMBL4107875 1 6.08
CHEMBL4113786 1 6.03
CHEMBL4110279 1 5.85
CHEMBL2386725 1 5.54
CHEMBL4108635 1 5.42
CHEMBL4115141 1 5.35
CHEMBL4110497 1 5.25
CHEMBL4108431 1 5.18
CHEMBL4107314 1 5.09
CHEMBL4115271 1 5.05
CHEMBL4111029 1 5.00
CHEMBL4108644 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2386724 IC50 = 4.0 nM 8.40
CHEMBL2386726 IC50 = 7.0 nM 8.15
CHEMBL4111699 IC50 = 27.0 nM 7.57
CHEMBL4115329 IC50 = 48.0 nM 7.32
CHEMBL4114267 IC50 = 66.0 nM 7.18
CHEMBL2386720 IC50 = 71.0 nM 7.15
CHEMBL4111654 IC50 = 93.0 nM 7.03
CHEMBL4106556 IC50 = 95.0 nM 7.02
CHEMBL4109969 IC50 = 120.0 nM 6.92
CHEMBL2386721 IC50 = 140.0 nM 6.85
CHEMBL4112589 IC50 = 260.0 nM 6.58
CHEMBL2386719 IC50 = 260.0 nM 6.58
CHEMBL2386723 IC50 = 290.0 nM 6.54
CHEMBL4109860 IC50 = 420.0 nM 6.38
CHEMBL4110655 IC50 = 490.0 nM 6.31
CHEMBL2386722 IC50 = 580.0 nM 6.24
CHEMBL4112705 IC50 = 580.0 nM 6.24
CHEMBL4110172 IC50 = 730.0 nM 6.14
CHEMBL4107875 IC50 = 840.0 nM 6.08
CHEMBL4113786 IC50 = 930.0 nM 6.03
CHEMBL4110279 IC50 = 1400.0 nM 5.85
CHEMBL2386725 IC50 = 2900.0 nM 5.54
CHEMBL4108635 IC50 = 3800.0 nM 5.42
CHEMBL4115141 IC50 = 4500.0 nM 5.35
CHEMBL4110497 IC50 = 5600.0 nM 5.25
CHEMBL4108431 IC50 = 6600.0 nM 5.18
CHEMBL4107314 IC50 = 8200.0 nM 5.09
CHEMBL4115271 IC50 = 8900.0 nM 5.05
CHEMBL4111029 IC50 = 10000.0 nM 5.00
CHEMBL4108644 IC50 > 10000.0 nM -
CHEMBL4111103 IC50 > 10000.0 nM -
CHEMBL4108335 IC50 > 10000.0 nM -
CHEMBL4114553 IC50 > 10000.0 nM -
CHEMBL3902027 IC50 > 10000.0 nM -
CHEMBL4114995 IC50 > 10000.0 nM -