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Assay Detail

CHEMBL4707713

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Functional
Antiproliferative activity against human G-361 cells assessed as cell viability measured after 4 days by MTT assay
13
Total Activities
13
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type G-361
Confidence 1 — Organism
Curated By Autocuration

Target

G-361 (CHEMBL614036)
Type CELL-LINE
Organism Homo sapiens

Publication

Antitumor agents 7. Synthesis, antiproliferative activity and molecular modeling of new l-lysine-conjugated pyridophenoxazinones as potent DNA-binding ligands and topoisomerase IIα inhibitors.
Pedatella,S.; Cerchia,C.; Manfra,M.; Cioce,A.; Bolognese,A.; Lavecchia,A.
Eur J Med Chem (2020) 187 : 111960 -111960
PubMed 31869654 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 13 7.43 9.00

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL4744840 1 9.00
CHEMBL4788620 1 8.22
CHEMBL1554 DACTINOMYCIN 4.0 1 8.22
CHEMBL151423 1 8.00
CHEMBL4756108 1 7.70
CHEMBL4780009 1 7.52
CHEMBL4792590 1 7.30
CHEMBL4740082 1 7.30
CHEMBL4743363 1 7.22
CHEMBL4786452 1 7.05
CHEMBL53463 DOXORUBICIN 4.0 1 7.05
CHEMBL346174 1 6.35
CHEMBL44657 ETOPOSIDE 4.0 1 5.64

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL4744840 IC50 = 1.0 nM 9.00
CHEMBL4788620 IC50 = 6.0 nM 8.22
CHEMBL1554 DACTINOMYCIN IC50 = 6.0 nM 8.22
CHEMBL151423 IC50 = 10.0 nM 8.00
CHEMBL4756108 IC50 = 20.0 nM 7.70
CHEMBL4780009 IC50 = 30.0 nM 7.52
CHEMBL4792590 IC50 = 50.0 nM 7.30
CHEMBL4740082 IC50 = 50.0 nM 7.30
CHEMBL4743363 IC50 = 60.0 nM 7.22
CHEMBL4786452 IC50 = 90.0 nM 7.05
CHEMBL53463 DOXORUBICIN IC50 = 90.0 nM 7.05
CHEMBL346174 IC50 = 450.0 nM 6.35
CHEMBL44657 ETOPOSIDE IC50 = 2300.0 nM 5.64