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Assay Detail

CHEMBL683177

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

Functional
In vitro cytotoxicity against human small cell lung carcinoma H69/P.
19
Total Activities
19
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type NCI-H69
Confidence 1 — Organism
Curated By Expert

Target

NCI-H69 (CHEMBL614805)
Type CELL-LINE
Organism Homo sapiens

Publication

Structure-activity relationships for analogues of the phenazine-based dual topoisomerase I/II inhibitor XR11576.
Wang S, Miller W, Milton J, Vicker N, Stewart A, Charlton P, Mistry P, Hardick D, Denny WA.
Bioorg Med Chem Lett (2002) 12 : 415 -418
PubMed 11814810 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 19 6.20 7.03

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL339173 1 7.03
CHEMBL134477 1 6.98
CHEMBL337416 1 6.59
CHEMBL134775 1 6.55
CHEMBL134166 1 6.46
CHEMBL132791 1 6.39
CHEMBL133871 1 6.38
CHEMBL132483 1 6.36
CHEMBL135956 1 6.35
CHEMBL335314 1 6.34
CHEMBL337866 1 6.30
CHEMBL131786 1 6.29
CHEMBL134662 1 6.28
CHEMBL134862 1 5.91
CHEMBL434034 1 5.74
CHEMBL132185 1 5.62
CHEMBL133530 1 5.41
CHEMBL424080 1 4.70
CHEMBL132838 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL339173 IC50 = 94.0 nM 7.03
CHEMBL134477 IC50 = 104.0 nM 6.98
CHEMBL337416 IC50 = 259.0 nM 6.59
CHEMBL134775 IC50 = 282.0 nM 6.55
CHEMBL134166 IC50 = 350.0 nM 6.46
CHEMBL132791 IC50 = 406.0 nM 6.39
CHEMBL133871 IC50 = 417.0 nM 6.38
CHEMBL132483 IC50 = 435.0 nM 6.36
CHEMBL135956 IC50 = 445.0 nM 6.35
CHEMBL335314 IC50 = 458.0 nM 6.34
CHEMBL337866 IC50 = 506.0 nM 6.30
CHEMBL131786 IC50 = 519.0 nM 6.29
CHEMBL134662 IC50 = 523.0 nM 6.28
CHEMBL134862 IC50 = 1223.0 nM 5.91
CHEMBL434034 IC50 = 1820.0 nM 5.74
CHEMBL132185 IC50 = 2400.0 nM 5.62
CHEMBL133530 IC50 = 3930.0 nM 5.41
CHEMBL424080 IC50 = 20000.0 nM 4.70
CHEMBL132838 IC50 > 100000.0 nM -