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Assay Detail

CHEMBL706362

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

Functional
Inhibition of cell proliferation of human lung small cell LXFS538 tumor xenograft in colony forming assay
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type LXFS538
Confidence 1 — Organism
Curated By Intermediate

Target

LXFS538 (CHEMBL614112)
Type CELL-LINE

Publication

Synthesis, cytotoxicity, and antitumor activity of copper(II) and iron(II) complexes of (4)N-azabicyclo[3.2.2]nonane thiosemicarbazones derived from acyl diazines.
Easmon J, Pürstinger G, Heinisch G, Roth T, Fiebig HH, Holzer W, Jäger W, Jenny M, Hofmann J.
J Med Chem (2001) 44 : 2164 -2171
PubMed 11405653 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 9.69 9.82

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL68899 1 9.82
CHEMBL303030 N-[(1E)-1-(5-methylpyrazin-2-yl)ethylidene]-3-azabicyclo[3.2.2]nonane-3-carbohydrazonothioic acid.chloro Cu(II)complex 1 9.74
CHEMBL307750 N-[(1E)-1-(6-methylpyrimidin-4-yl)ethylidene]-3-azabicyclo[3.2.2]nonane-3-carbohydrazonothioic acid.chloro Cu(II)complex 1 9.72
CHEMBL71931 N-[(1E)-1-(3-methylpyrazin-2-yl)ethylidene]-3-azabicyclo[3.2.2]nonane-3-carbohydrazonothioic acid.chloro Cu(II)complex 1 9.66
CHEMBL307351 1 9.62
CHEMBL68043 1 9.55

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL68899 IC50 = 0.15 nM 9.82
CHEMBL303030 N-[(1E)-1-(5-methylpyrazin-2-yl)ethylidene]-3-azabicyclo[3.2.2]nonane-3-carbohydrazonothioic acid.chloro Cu(II)complex IC50 = 0.18 nM 9.74
CHEMBL307750 N-[(1E)-1-(6-methylpyrimidin-4-yl)ethylidene]-3-azabicyclo[3.2.2]nonane-3-carbohydrazonothioic acid.chloro Cu(II)complex IC50 = 0.19 nM 9.72
CHEMBL71931 N-[(1E)-1-(3-methylpyrazin-2-yl)ethylidene]-3-azabicyclo[3.2.2]nonane-3-carbohydrazonothioic acid.chloro Cu(II)complex IC50 = 0.22 nM 9.66
CHEMBL307351 IC50 = 0.24 nM 9.62
CHEMBL68043 IC50 = 0.28 nM 9.55