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Assay Detail

CHEMBL935694

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Functional
Cytotoxicity against human P388 cells
11
Total Activities
11
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type P388
Confidence 1 — Organism
Curated By Autocuration

Target

P388 (CHEMBL389)
Type CELL-LINE
Organism Mus musculus

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 10.24 10.92

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL256099 1 10.92
CHEMBL255716 1 10.72
CHEMBL256302 1 10.52
CHEMBL257360 1 10.46
CHEMBL257572 1 10.40
CHEMBL257629 1 9.72
CHEMBL428603 1 9.70
CHEMBL257361 1 9.48
CHEMBL65 CAMPTOTHECIN -1.0 1 -
CHEMBL71086 1 -
CHEMBL70790 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL256099 IC50 = 0.012 nM 10.92
CHEMBL255716 IC50 = 0.019 nM 10.72
CHEMBL256302 IC50 = 0.03 nM 10.52
CHEMBL257360 IC50 = 0.035 nM 10.46
CHEMBL257572 IC50 = 0.04 nM 10.40
CHEMBL257629 IC50 = 0.19 nM 9.72
CHEMBL428603 IC50 = 0.2 nM 9.70
CHEMBL257361 IC50 = 0.33 nM 9.48
CHEMBL65 CAMPTOTHECIN IC50 = 0.004 nM -
CHEMBL71086 IC50 = 0.002 nM -
CHEMBL70790 IC50 = 0.001 nM -