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Assay Detail

CHEMBL829497

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

Binding
Inhibitory concentration against Butyrylcholinesterase from human erythrocytes
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Expert

Target

Cholinesterase (CHEMBL1914)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and pharmacological evaluation of huprine-tacrine heterodimers: subnanomolar dual binding site acetylcholinesterase inhibitors.
Camps P, Formosa X, Muñoz-Torrero D, Petrignet J, Badia A, Clos MV.
J Med Chem (2005) 48 : 1701 -1704
PubMed 15771413 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 8.03 8.32

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL534932 1 8.32
CHEMBL535812 1 8.26
CHEMBL557155 1 8.17
CHEMBL538573 1 8.13
CHEMBL555666 1 8.11
CHEMBL539599 1 8.11
CHEMBL555214 1 7.85
CHEMBL2113368 1 7.79
CHEMBL2113367 1 7.51

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL534932 IC50 = 4.74 nM 8.32
CHEMBL535812 IC50 = 5.55 nM 8.26
CHEMBL557155 IC50 = 6.7 nM 8.17
CHEMBL538573 IC50 = 7.38 nM 8.13
CHEMBL555666 IC50 = 7.69 nM 8.11
CHEMBL539599 IC50 = 7.8 nM 8.11
CHEMBL555214 IC50 = 14.0 nM 7.85
CHEMBL2113368 IC50 = 16.4 nM 7.79
CHEMBL2113367 IC50 = 31.1 nM 7.51