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Assay Detail

CHEMBL3887854

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Binding
Inhibition Assay: AChE inhibitory activity of compounds (Ia)-(Ie) and (-)-(Ib) and (+)-(Ib) was evaluated spectrophotometrically at 25° C. by the method of Ellman et al., using recombinant human AChE (hAChE) and Electrophorus electricus (ee) AChE and acetylthiocholine iodide as substrate (cf. G. L. Ellman et al., New and Rapid Colorimetric Determination of Acetylcholinesterase Activity Biochem. Pharmacol. 1961, vol. 7, pp. 88-95). For eeAChE inhibitory activity determination, the reaction took place in a final volume of 300 uL of 0.1 M phosphate-buffered solution pH 8.0, containing 0.03 unit/mL of ee AChE and 333 uM 5,5'-dithiobis(2-nitrobenzoic) acid (DTNB) solution used to produce the yellow anion of 5-thio-2-nitrobenzoic acid. Inhibition curves were performed in duplicates using at least 10 increasing concentrations of inhibitor and preincubating at 37° C. for 20 min. One duplicate sample without inhibitor was always present to yield 100% of AChE activity. Then, substrate acetylthiocholine (450 uM) was added and the reaction was developed at 37° C. for 5 min. The color production was measured at 414 nm.
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Acetylcholinesterase (CHEMBL4078)
Type SINGLE PROTEIN
Organism Electrophorus electricus

Publication

Beta-amyloid-directed multitarget compounds for the treatment of alzheimer's disease
(2016)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 7.71 10.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1161905 1 10.22
CHEMBL140476 HUPRINE Y 1 10.10
CHEMBL4113560 1 8.03
CHEMBL3304241 1 7.79
CHEMBL3304306 1 7.49
CHEMBL3303094 1 7.33
CHEMBL3304178 1 7.22
CHEMBL3304357 1 7.05
CHEMBL4109726 1 7.00
CHEMBL4112162 1 6.43
CHEMBL418068 RHEIN 1 6.20

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1161905 IC50 = 0.06 nM 10.22
CHEMBL140476 HUPRINE Y IC50 = 0.08 nM 10.10
CHEMBL4113560 IC50 = 9.4 nM 8.03
CHEMBL3304241 IC50 = 16.3 nM 7.79
CHEMBL3304306 IC50 = 32.6 nM 7.49
CHEMBL3303094 IC50 = 46.7 nM 7.33
CHEMBL3304178 IC50 = 60.0 nM 7.22
CHEMBL3304357 IC50 = 88.6 nM 7.05
CHEMBL4109726 IC50 = 98.9 nM 7.00
CHEMBL4112162 IC50 = 373.0 nM 6.43
CHEMBL418068 RHEIN IC50 = 637.0 nM 6.20