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Assay Detail

CHEMBL1049243

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

Binding
Inhibition of human serum AChE by Ellman's assay
10
Total Activities
10
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

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

Target

Acetylcholinesterase (CHEMBL220)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Active site directed docking studies: synthesis and pharmacological evaluation of cis-2,6-dimethyl piperidine sulfonamides as inhibitors of acetylcholinesterase.
Girisha HR, Narendra Sharath Chandra JN, Boppana S, Malviya M, Sadashiva CT, Rangappa KS.
Eur J Med Chem (2009) 44 : 4057 -4062
PubMed 19493592 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 10 6.66 7.39

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL54126 NEOSTIGMINE BROMIDE 2.0 1 7.39
CHEMBL576005 1 7.12
CHEMBL582883 1 7.05
CHEMBL575813 1 6.73
CHEMBL574474 1 6.72
CHEMBL573102 1 6.50
CHEMBL575620 1 6.43
CHEMBL575619 1 6.41
CHEMBL575621 1 6.34
CHEMBL574487 1 5.94

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL54126 NEOSTIGMINE BROMIDE IC50 = 41.0 nM 7.39
CHEMBL576005 IC50 = 75.0 nM 7.12
CHEMBL582883 IC50 = 90.0 nM 7.05
CHEMBL575813 IC50 = 185.0 nM 6.73
CHEMBL574474 IC50 = 192.0 nM 6.72
CHEMBL573102 IC50 = 318.0 nM 6.50
CHEMBL575620 IC50 = 368.0 nM 6.43
CHEMBL575619 IC50 = 392.0 nM 6.41
CHEMBL575621 IC50 = 458.0 nM 6.34
CHEMBL574487 IC50 = 1150.0 nM 5.94