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Assay Detail

CHEMBL935693

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Functional
Cytotoxicity against human camptothecin-resistant CPT-K5 cells
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type CPT-K5
Confidence 1 — Organism
Curated By Autocuration

Publication

Facile formation of hydrophilic derivatives of 5H-8,9-dimethoxy-5-[2-(N,N-dimethylamino)ethyl]-2,3-methylenedioxydibenzo[c,h] [1,6]naphthyridin-6-one (ARC-111) and its 12-aza analog via quaternary ammonium intermediates.
Feng W, Satyanarayana M, Tsai YC, Liu AA, Liu LF, Lavoie EJ.
Bioorg Med Chem Lett (2008) 18 : 3570 -3572
PubMed 18511275 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 11 8.68 9.13

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL71086 1 9.13
CHEMBL70790 1 9.05
CHEMBL256099 1 8.89
CHEMBL255716 1 8.66
CHEMBL257360 1 8.66
CHEMBL257572 1 8.24
CHEMBL257361 1 8.15
CHEMBL256302 1 -
CHEMBL257629 1 -
CHEMBL428603 1 -
CHEMBL65 CAMPTOTHECIN -1.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL71086 IC50 = 0.74 nM 9.13
CHEMBL70790 IC50 = 0.9 nM 9.05
CHEMBL256099 IC50 = 1.3 nM 8.89
CHEMBL255716 IC50 = 2.2 nM 8.66
CHEMBL257360 IC50 = 2.2 nM 8.66
CHEMBL257572 IC50 = 5.7 nM 8.24
CHEMBL257361 IC50 = 7.0 nM 8.15
CHEMBL256302 IC50 > 10.0 nM -
CHEMBL257629 IC50 > 10.0 nM -
CHEMBL428603 IC50 > 10.0 nM -
CHEMBL65 CAMPTOTHECIN IC50 > 10.0 nM -