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Assay Detail

CHEMBL659267

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

Binding
The compound was evaluated for the inhibition human of Butyrylcholinesterase I
9
Total Activities
9
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Cholinesterase (CHEMBL1914)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Synthesis and cholinergic properties of bis[[(dimethylamino)methyl]furanyl] analogues of ranitidine.
Sowell JW, Tang Y, Valli MJ, Chapman JM, Usher LA, Vaughan CM, Kosh JW.
J Med Chem (1992) 35 : 1102 -1108
PubMed 1552502 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 9 5.77 7.64

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL95 TACRINE 4.0 1 7.64
CHEMBL12781 1 5.89
CHEMBL12858 1 5.62
CHEMBL12472 1 5.57
CHEMBL268499 1 5.54
CHEMBL12937 1 5.51
CHEMBL13166 1 5.44
CHEMBL275537 1 5.39
CHEMBL13308 1 5.37

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL95 TACRINE IC50 = 23.0 nM 7.64
CHEMBL12781 IC50 = 1300.0 nM 5.89
CHEMBL12858 IC50 = 2400.0 nM 5.62
CHEMBL12472 IC50 = 2700.0 nM 5.57
CHEMBL268499 IC50 = 2900.0 nM 5.54
CHEMBL12937 IC50 = 3100.0 nM 5.51
CHEMBL13166 IC50 = 3600.0 nM 5.44
CHEMBL275537 IC50 = 4100.0 nM 5.39
CHEMBL13308 IC50 = 4300.0 nM 5.37