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Assay Detail

CHEMBL5049503

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

Binding
Inhibition of recombinant His-TEV-tagged human AChE expressed in CHO-K1 cells using acetylthiocholine iodide as substrate measured for 6 mins by Ellman's method
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type CHO-K1
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Acetylcholinesterase (CHEMBL220)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

A New Class of Bi- and Trifunctional Sugar Oximes as Antidotes against Organophosphorus Poisoning.
Da Silva O, Probst N, Landry C, Hanak AS, Warnault P, Coisne C, Calas AG, Gosselet F, Courageux C, Gastellier AJ, Trancart M, Baati R, Dehouck MP, Jean L, Nachon F, Renard PY, Dias J.
J Med Chem (2022) 65 : 4649 -4666
PubMed 35255209 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 4.26 4.26

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL33051 1 4.26
CHEMBL5084128 1 -
CHEMBL5069796 1 -
CHEMBL5088176 1 -
CHEMBL1420 PRALIDOXIME 4.0 1 -
CHEMBL291233 OBIDOXIME CHLORIDE 2.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL33051 IC50 = 55000.0 nM 4.26
CHEMBL5084128 IC50 = 140000.0 nM -
CHEMBL5069796 IC50 = 1600000.0 nM -
CHEMBL5088176 IC50 = 580000.0 nM -
CHEMBL1420 PRALIDOXIME IC50 = 560000.0 nM -
CHEMBL291233 OBIDOXIME CHLORIDE IC50 = 640000.0 nM -