Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL5259702

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

Toxicity
Cytotoxicity against human EA.hy 926 cells assessed as inhibition of cell growth measured after 48 to 72 hrs by MTT assay
3
Total Activities
3
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Toxicity
Organism Homo sapiens
Cell Type EA.hy 926
Confidence 1 — Organism
Curated By Autocuration

Target

EA.hy 926 (CHEMBL4296410)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and evaluation of sulfonamide derivatives targeting EGFR<sup>790M/L858R</sup> mutations and ALK rearrangement as anticancer agents.
Cao L, Yao H, Yu L, Ren Y, Liu J, Li X, Jia X.
Bioorg Med Chem (2023) 85 : 117241 -117241
PubMed 37087886 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 3 5.91 6.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2403108 CERITINIB 4.0 1 6.00
CHEMBL3353410 OSIMERTINIB 4.0 1 5.93
CHEMBL5284780 1 5.79

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2403108 CERITINIB IC50 = 1010.0 nM 6.00
CHEMBL3353410 OSIMERTINIB IC50 = 1161.0 nM 5.93
CHEMBL5284780 IC50 = 1609.0 nM 5.79