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Assay Detail

CHEMBL5116799

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

Functional
Cytotoxicity against ER/PR-negative HER2-positive human SK-BR-3 cells harbouring wild type p53 assessed as inhibition of cell growth incubated for 48 hrs by resazurin dye based assay
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type SK-BR-3
Confidence 1 — Organism
Curated By Autocuration

Target

SK-BR-3 (CHEMBL613834)
Type CELL-LINE
Organism Homo sapiens

Publication

Design, synthesis and biological evaluation of novel aminopropylcarboxamide derivatives as sigma ligands.
Zampieri D, Fortuna S, Romano M, Amata E, Dichiara M, Marrazzo A, Pasquinucci L, Turnaturi R, Mamolo MG.
Bioorg Med Chem Lett (2022) 72 : 128860 -128860
PubMed 35724925 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 4.41 4.85

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL61479 SIRAMESINE 2.0 1 4.85
CHEMBL5182253 1 4.46
CHEMBL5169420 1 4.28
CHEMBL5187029 1 4.06
CHEMBL5201355 1 -
CHEMBL54 HALOPERIDOL 4.0 1 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL61479 SIRAMESINE IC50 = 14000.0 nM 4.85
CHEMBL5182253 IC50 = 35000.0 nM 4.46
CHEMBL5169420 IC50 = 52000.0 nM 4.28
CHEMBL5187029 IC50 = 88000.0 nM 4.06
CHEMBL5201355 IC50 = 169000.0 nM -
CHEMBL54 HALOPERIDOL IC50 = 131000.0 nM -