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Assay Detail

CHEMBL1011675

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

Binding
Inhibition of human ERG td[wt:F656A] mutant expressed in HEK293 cells by whole cell patch clamp method
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HEK293
Confidence 0 — Uncurated / Unknown
Curated By Autocuration

Target

Unchecked (CHEMBL612545)
Type UNCHECKED

Publication

Docking model of drug binding to the human ether-à-go-go potassium channel guided by tandem dimer mutant patch-clamp data: a synergic approach.
Imai YN, Ryu S, Oiki S.
J Med Chem (2009) 52 : 1630 -1638
PubMed 19260734 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 7.74 8.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1729 CISAPRIDE 4.0 1 8.00
CHEMBL536480 1 7.70
CHEMBL17157 TERFENADINE 4.0 1 7.52

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1729 CISAPRIDE IC50 = 10.0 nM 8.00
CHEMBL536480 IC50 = 20.0 nM 7.70
CHEMBL17157 TERFENADINE IC50 = 30.0 nM 7.52