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Assay Detail

CHEMBL4821236

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

Functional
Cytotoxicity against human A549 cells incubated for 2 to 4 hrs by MTT assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type A549
Confidence 1 — Organism
Curated By Autocuration

Target

A549 (CHEMBL392)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and assessment of new series of quinazolinone derivatives as EGFR inhibitors along with their cytotoxic evaluation against MCF7 and A549 cancer cell lines.
Aziz MW, Kamal AM, Mohamed KO, Elgendy AA.
Bioorg Med Chem Lett (2021) 41 : 127987 -127987
PubMed 33771586 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 5.15 6.14

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4866476 1 6.14
CHEMBL4859473 1 5.68
CHEMBL4877452 1 5.49
CHEMBL939 GEFITINIB 4.0 1 5.45
CHEMBL4849859 1 5.28
CHEMBL1988225 1 5.14
CHEMBL553 ERLOTINIB 4.0 1 5.00
CHEMBL4865719 1 4.88
CHEMBL4873968 1 4.67
CHEMBL4869732 1 4.60
CHEMBL4855214 1 4.35
CHEMBL1969820 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4866476 IC50 = 720.0 nM 6.14
CHEMBL4859473 IC50 = 2100.0 nM 5.68
CHEMBL4877452 IC50 = 3220.0 nM 5.49
CHEMBL939 GEFITINIB IC50 = 3530.0 nM 5.45
CHEMBL4849859 IC50 = 5310.0 nM 5.28
CHEMBL1988225 IC50 = 7290.0 nM 5.14
CHEMBL553 ERLOTINIB IC50 = 10000.0 nM 5.00
CHEMBL4865719 IC50 = 13300.0 nM 4.88
CHEMBL4873968 IC50 = 21300.0 nM 4.67
CHEMBL4869732 IC50 = 25000.0 nM 4.60
CHEMBL4855214 IC50 = 44700.0 nM 4.35
CHEMBL1969820 IC50 = 187000.0 nM -