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Assay Detail

CHEMBL837533

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

Functional
Cytotoxicity against human PC3 cancer cell line was determined after 144 hr
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type PC-3
Confidence 1 — Organism
Curated By Intermediate

Target

PC-3 (CHEMBL390)
Type CELL-LINE
Organism Homo sapiens

Publication

Rational design, synthesis, and biological evaluation of bis(pyrimido[5,6,1-de]acridines) and bis(pyrazolo[3,4,5-kl]acridine-5-carboxamides) as new anticancer agents.
Antonini I, Polucci P, Magnano A, Sparapani S, Martelli S.
J Med Chem (2004) 47 : 5244 -5250
PubMed 15456268 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 8.68 11.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL187738 1 11.00
CHEMBL188103 1 8.92
CHEMBL186004 1 8.35
CHEMBL362087 1 8.22
CHEMBL58 MITOXANTRONE 4.0 1 8.15
CHEMBL189214 1 7.41

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL187738 IC50 = 0.01 nM 11.00
CHEMBL188103 IC50 = 1.2 nM 8.92
CHEMBL186004 IC50 = 4.5 nM 8.35
CHEMBL362087 IC50 = 6.0 nM 8.22
CHEMBL58 MITOXANTRONE IC50 = 7.0 nM 8.15
CHEMBL189214 IC50 = 39.0 nM 7.41