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Assay Detail

CHEMBL815077

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Functional
In vitro antitumor effects against human U-373MG cell lines.
17
Total Activities
17
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type U-373MG ATCC
Confidence 1 — Organism
Curated By Expert

Target

U373 MG (CHEMBL615024)
Type CELL-LINE
Organism Homo sapiens

Publication

Synthesis and in vitro antitumor activity of phenanthrolin-7-one derivatives, analogues of the marine pyridoacridine alkaloids ascididemin and meridine: structure-activity relationship.
Delfourne E, Kiss R, Le Corre L, Dujols F, Bastide J, Collignon F, Lesur B, Frydman A, Darro F.
J Med Chem (2003) 46 : 3536 -3545
PubMed 12877592 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 17 5.93 8.15

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL119700 1 8.15
CHEMBL117427 1 7.16
CHEMBL117784 1 7.00
CHEMBL118655 1 6.22
CHEMBL333433 1 6.10
CHEMBL325202 1 6.10
CHEMBL334217 1 6.10
CHEMBL331163 1 6.00
CHEMBL118709 1 5.70
CHEMBL117616 1 5.40
CHEMBL334029 1 5.40
CHEMBL119393 1 5.30
CHEMBL119894 1 5.30
CHEMBL331562 1 5.22
CHEMBL118845 1 5.22
CHEMBL118201 1 5.22
CHEMBL119037 1 5.22

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL119700 IC50 = 7.0 nM 8.15
CHEMBL117427 IC50 = 70.0 nM 7.16
CHEMBL117784 IC50 = 100.0 nM 7.00
CHEMBL118655 IC50 = 600.0 nM 6.22
CHEMBL333433 IC50 = 800.0 nM 6.10
CHEMBL325202 IC50 = 800.0 nM 6.10
CHEMBL334217 IC50 = 800.0 nM 6.10
CHEMBL331163 IC50 = 1000.0 nM 6.00
CHEMBL118709 IC50 = 2000.0 nM 5.70
CHEMBL117616 IC50 = 4000.0 nM 5.40
CHEMBL334029 IC50 = 4000.0 nM 5.40
CHEMBL119393 IC50 = 5000.0 nM 5.30
CHEMBL119894 IC50 = 5000.0 nM 5.30
CHEMBL331562 IC50 = 6000.0 nM 5.22
CHEMBL118845 IC50 = 6000.0 nM 5.22
CHEMBL118201 IC50 = 6000.0 nM 5.22
CHEMBL119037 IC50 = 6000.0 nM 5.22