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Assay Detail

CHEMBL2434702

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

Functional
Cytotoxicity against human DU145 cells assessed as cell viability after 72 hrs by MTS assay
12
Total Activities
12
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type DU-145
Confidence 1 — Organism
Curated By Autocuration

Target

DU-145 (CHEMBL613508)
Type CELL-LINE
Organism Homo sapiens

Publication

Inhibiting aberrant signal transducer and activator of transcription protein activation with tetrapodal, small molecule Src homology 2 domain binders: promising agents against multiple myeloma.
Page BD, Croucher DC, Li ZH, Haftchenary S, Jimenez-Zepeda VH, Atkinson J, Spagnuolo PA, Wong YL, Colaguori R, Lewis AM, Schimmer AD, Trudel S, Gunning PT.
J Med Chem (2013) 56 : 7190 -7200
PubMed 23968501 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 12 4.78 5.04

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL2431935 1 5.04
CHEMBL2431952 1 5.02
CHEMBL2431941 1 4.96
CHEMBL2431955 1 4.85
CHEMBL2431993 1 4.80
CHEMBL2431995 1 4.77
CHEMBL2431990 1 4.77
CHEMBL2431957 1 4.72
CHEMBL2431994 1 4.72
CHEMBL1829876 1 4.64
CHEMBL2431956 1 4.57
CHEMBL1829786 1 4.46

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL2431935 IC50 = 9100.0 nM 5.04
CHEMBL2431952 IC50 = 9500.0 nM 5.02
CHEMBL2431941 IC50 = 11000.0 nM 4.96
CHEMBL2431955 IC50 = 14000.0 nM 4.85
CHEMBL2431993 IC50 = 16000.0 nM 4.80
CHEMBL2431995 IC50 = 17000.0 nM 4.77
CHEMBL2431990 IC50 = 17000.0 nM 4.77
CHEMBL2431957 IC50 = 19000.0 nM 4.72
CHEMBL2431994 IC50 = 19000.0 nM 4.72
CHEMBL1829876 IC50 = 23000.0 nM 4.64
CHEMBL2431956 IC50 = 27000.0 nM 4.57
CHEMBL1829786 IC50 = 35000.0 nM 4.46