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Assay Detail

CHEMBL5142617

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

Binding
Inhibition of human BChE assessed as inhibition constant
5
Total Activities
5
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

Cholinesterase (CHEMBL1914)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

<i>N</i>-Benzyl Benzamide Derivatives as Selective Sub-Nanomolar Butyrylcholinesterase Inhibitors for Possible Treatment in Advanced Alzheimer's Disease.
Du C, Wang L, Guan Q, Yang H, Chen T, Liu Y, Li Q, Lyu W, Lu X, Chen Y, Liu Y, Liu H, Feng F, Liu W, Liu Z, Li W, Chen Y, Sun H.
J Med Chem (2022) 65 : 11365 -11387
PubMed 35969197 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
Ki 5 7.88 10.03

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5201089 1 10.03
CHEMBL5195228 1 9.21
CHEMBL1206 ETHOPROPAZINE 4.0 1 7.70
CHEMBL332935 1 6.37
CHEMBL224392 THIOFLAVIN T 1 6.10

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5201089 Ki = 0.094 nM 10.03
CHEMBL5195228 Ki = 0.61 nM 9.21
CHEMBL1206 ETHOPROPAZINE Ki = 20.0 nM 7.70
CHEMBL332935 Ki = 430.0 nM 6.37
CHEMBL224392 THIOFLAVIN T Ki = 800.0 nM 6.10