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Assay Detail

CHEMBL1932399

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

Functional
Cytotoxicity against human MCF7 cells after 4 days by propidium iodide staining-based fluorometric analysis
6
Total Activities
6
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type MCF7
Confidence 1 — Organism
Curated By Autocuration

Target

MCF7 (CHEMBL387)
Type CELL-LINE
Organism Homo sapiens

Publication

Novel inhibitors of epidermal growth factor receptor: (4-(Arylamino)-7H-pyrrolo[2,3-d]pyrimidin-6-yl)(1H-indol-2-yl)methanones and (1H-indol-2-yl)(4-(phenylamino)thieno[2,3-d]pyrimidin-6-yl)methanones.
Beckers T, Sellmer A, Eichhorn E, Pongratz H, Schächtele C, Totzke F, Kelter G, Krumbach R, Fiebig HH, Böhmer FD, Mahboobi S.
Bioorg Med Chem (2012) 20 : 125 -136
PubMed 22169601 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 6 4.95 5.38

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL1928311 1 5.38
CHEMBL554 LAPATINIB 4.0 1 5.32
CHEMBL1928291 1 5.16
CHEMBL1928312 1 4.95
CHEMBL1928309 1 4.90
CHEMBL553 ERLOTINIB 4.0 1 4.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL1928311 IC50 = 4220.0 nM 5.38
CHEMBL554 LAPATINIB IC50 = 4830.0 nM 5.32
CHEMBL1928291 IC50 = 6960.0 nM 5.16
CHEMBL1928312 IC50 = 11300.0 nM 4.95
CHEMBL1928309 IC50 = 12500.0 nM 4.90
CHEMBL553 ERLOTINIB IC50 = 100000.0 nM 4.00