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Assay Detail

CHEMBL3706090

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Binding
Inhibition Assay: Zero point five μL of the test compounds (dissolved in N,N′-dimethylsulfoxide) were incubated with 48.5 μL of the fluorescence-quenched peptide substrate solution (Biotin-XSEVNLDAEFRHDSGC-Eu: X=εe-amino-n-capronic acid,Eu=Europium cryptate) and 1 μL of recombinant human BACE-1 protein (R&D systems) for 3 h at 30° C. in the 96 well half-area plate (black color plate,Costar). The substrate peptide was synthesized by reacting with Biotin-XSEVNLDAEFRHDSGC (Peptide Institute) and Cryptate TBPCOOH mono SMP (CIS bio international). The final concentration of the substrate peptide and recombinant human BACE-1 protein were 18 nM and 7.4 nM, respectively. The enzymatic reaction was performed in sodium acetate buffer (50 mM sodium acetate (pH 5.0), 0.008% Triton X-100). After the reaction, a 50 μL of 8.0 μg/mL Streptavidin-XL665 (CIS bio international) dissolved in phosphate buffer (150 mM K2HPO4KH2PO4 (pH 7.0), 0.008% Triton X-100, 0.8 M KF) was added.
60
Total Activities
60
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

Beta-secretase 1 (CHEMBL4822)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Aminodihydrothiazine derivatives
(2014)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 60 6.09 7.57

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3645171 1 7.57
CHEMBL3645172 1 7.50
CHEMBL3645168 1 7.43
CHEMBL3642600 1 7.41
CHEMBL3645166 1 7.31
CHEMBL3645174 1 7.27
CHEMBL3642627 1 7.21
CHEMBL3937030 1 6.89
CHEMBL3642623 1 6.85
CHEMBL3642607 1 6.83
CHEMBL3642611 1 6.81
CHEMBL3645170 1 6.80
CHEMBL3645164 1 6.79
CHEMBL3642625 1 6.78
CHEMBL3645163 1 6.78
CHEMBL3645177 1 6.76
CHEMBL1241578 1 6.76
CHEMBL1233882 1 6.66
CHEMBL3645167 1 6.65
CHEMBL1241481 1 6.64
CHEMBL3645165 1 6.61
CHEMBL3642626 1 6.58
CHEMBL3642604 1 6.56
CHEMBL3645173 1 6.36
CHEMBL3642614 1 6.35
CHEMBL3645169 1 6.30
CHEMBL3642619 1 6.14
CHEMBL3642613 1 6.09
CHEMBL3645175 1 6.08
CHEMBL3642632 1 6.04

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3645171 IC50 = 27.0 nM 7.57
CHEMBL3645172 IC50 = 32.0 nM 7.50
CHEMBL3645168 IC50 = 37.0 nM 7.43
CHEMBL3642600 IC50 = 39.4 nM 7.41
CHEMBL3645166 IC50 = 49.0 nM 7.31
CHEMBL3645174 IC50 = 54.0 nM 7.27
CHEMBL3642627 IC50 = 61.0 nM 7.21
CHEMBL3937030 IC50 = 130.0 nM 6.89
CHEMBL3642623 IC50 = 140.0 nM 6.85
CHEMBL3642607 IC50 = 149.0 nM 6.83
CHEMBL3642611 IC50 = 156.0 nM 6.81
CHEMBL3645170 IC50 = 160.0 nM 6.80
CHEMBL3645164 IC50 = 163.0 nM 6.79
CHEMBL3645163 IC50 = 165.0 nM 6.78
CHEMBL3642625 IC50 = 165.0 nM 6.78
CHEMBL3645177 IC50 = 174.0 nM 6.76
CHEMBL1241578 IC50 = 175.0 nM 6.76
CHEMBL1233882 IC50 = 220.0 nM 6.66
CHEMBL3645167 IC50 = 222.0 nM 6.65
CHEMBL1241481 IC50 = 229.0 nM 6.64
CHEMBL3645165 IC50 = 243.0 nM 6.61
CHEMBL3642626 IC50 = 264.0 nM 6.58
CHEMBL3642604 IC50 = 278.0 nM 6.56
CHEMBL3645173 IC50 = 435.0 nM 6.36
CHEMBL3642614 IC50 = 450.0 nM 6.35
CHEMBL3645169 IC50 = 505.0 nM 6.30
CHEMBL3642619 IC50 = 720.0 nM 6.14
CHEMBL3642613 IC50 = 816.0 nM 6.09
CHEMBL3645175 IC50 = 833.0 nM 6.08
CHEMBL3642632 IC50 = 912.0 nM 6.04
CHEMBL3642629 IC50 = 930.0 nM 6.03
CHEMBL3642628 IC50 = 1288.0 nM 5.89
CHEMBL3642637 IC50 = 1479.0 nM 5.83
CHEMBL3642624 IC50 = 1500.0 nM 5.82
CHEMBL3642633 IC50 = 1500.0 nM 5.82
CHEMBL1570219 IC50 = 1977.0 nM 5.70
CHEMBL3645176 IC50 = 2296.0 nM 5.64
CHEMBL584726 IC50 = 2278.0 nM 5.64
CHEMBL3642606 IC50 = 2500.0 nM 5.60
CHEMBL3642618 IC50 = 2563.0 nM 5.59
CHEMBL3642617 IC50 = 2800.0 nM 5.55
CHEMBL3642601 IC50 = 2900.0 nM 5.54
CHEMBL1376633 IC50 = 3239.0 nM 5.49
CHEMBL3642636 IC50 = 3642.0 nM 5.44
CHEMBL3642622 IC50 = 4000.0 nM 5.40
CHEMBL3955419 IC50 = 4500.0 nM 5.35
CHEMBL3642635 IC50 = 4586.0 nM 5.34
CHEMBL3949846 IC50 = 5000.0 nM 5.30
CHEMBL3642605 IC50 = 5100.0 nM 5.29
CHEMBL3642610 IC50 = 5600.0 nM 5.25