Skip to main content
Free research Free research Free assay review with research home and workspace preview
Quick search ChEMBL 36
Assay Detail

CHEMBL2412943

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

Functional
Cytotoxicity against human HCT116 cells assessed as growth inhibition by measuring cellular ATP level after 72 hrs by cell-titer glo assay
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HCT-116
Confidence 1 — Organism
Curated By Autocuration

Target

HCT-116 (CHEMBL394)
Type CELL-LINE
Organism Homo sapiens

Publication

Discovery of potent, isoform-selective inhibitors of histone deacetylase containing chiral heterocyclic capping groups and a N-(2-aminophenyl)benzamide binding unit.
Marson CM, Matthews CJ, Yiannaki E, Atkinson SJ, Soden PE, Shukla L, Lamadema N, Thomas NS.
J Med Chem (2013) 56 : 6156 -6174
PubMed 23829483 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.48 6.16

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL272980 MOCETINOSTAT 2.0 1 6.16
CHEMBL98 VORINOSTAT 4.0 1 5.86
CHEMBL2407720 1 5.71
CHEMBL2407717 1 5.66
CHEMBL2407737 1 5.44
CHEMBL2407735 1 4.78
CHEMBL2407736 1 4.74

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL272980 MOCETINOSTAT IC50 = 700.0 nM 6.16
CHEMBL98 VORINOSTAT IC50 = 1390.0 nM 5.86
CHEMBL2407720 IC50 = 1950.0 nM 5.71
CHEMBL2407717 IC50 = 2170.0 nM 5.66
CHEMBL2407737 IC50 = 3640.0 nM 5.44
CHEMBL2407735 IC50 = 16600.0 nM 4.78
CHEMBL2407736 IC50 = 18200.0 nM 4.74