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Assay Detail

CHEMBL2411333

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

Functional
Cytotoxicity against human A549 cells after 72 hrs by sulforhodamine B assay
8
Total Activities
8
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

Naphthalimides exhibit in vitro antiproliferative and antiangiogenic activities by inhibiting both topoisomerase II (topo II) and receptor tyrosine kinases (RTKs).
Wang X, Chen Z, Tong L, Tan S, Zhou W, Peng T, Han K, Ding J, Xie H, Xu Y.
Eur J Med Chem (2013) 65 : 477 -486
PubMed 23770449 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 8 4.83 5.50

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL428676 AMONAFIDE 3.0 1 5.50
CHEMBL598852 1 5.11
CHEMBL2407519 1 5.01
CHEMBL598022 1 4.72
CHEMBL2407518 1 4.67
CHEMBL2407516 1 4.61
CHEMBL2407635 1 4.50
CHEMBL2407517 1 4.50

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL428676 AMONAFIDE IC50 = 3200.0 nM 5.50
CHEMBL598852 IC50 = 7800.0 nM 5.11
CHEMBL2407519 IC50 = 9800.0 nM 5.01
CHEMBL598022 IC50 = 19100.0 nM 4.72
CHEMBL2407518 IC50 = 21400.0 nM 4.67
CHEMBL2407516 IC50 = 24500.0 nM 4.61
CHEMBL2407635 IC50 = 31300.0 nM 4.50
CHEMBL2407517 IC50 = 31400.0 nM 4.50