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Assay Detail

CHEMBL687679

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

Functional
Concentration required for the antiproliferation of Human HT1080 fibrosarcoma cells
7
Total Activities
7
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Functional
Organism Homo sapiens
Cell Type HT-1080
Confidence 1 — Organism
Curated By Intermediate

Target

HT-1080 (CHEMBL614580)
Type CELL-LINE
Organism Homo sapiens

Publication

Succinimide hydroxamic acids as potent inhibitors of histone deacetylase (HDAC).
Curtin ML, Garland RB, Heyman HR, Frey RR, Michaelides MR, Li J, Pease LJ, Glaser KB, Marcotte PA, Davidsen SK.
Bioorg Med Chem Lett (2002) 12 : 2919 -2923
PubMed 12270175 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 7 5.89 6.60

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL329977 1 6.60
CHEMBL328819 1 6.40
CHEMBL317614 1 6.28
CHEMBL317734 1 5.82
CHEMBL98748 1 5.64
CHEMBL98 VORINOSTAT 4.0 1 5.62
CHEMBL98428 1 4.85

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL329977 IC50 = 250.0 nM 6.60
CHEMBL328819 IC50 = 400.0 nM 6.40
CHEMBL317614 IC50 = 530.0 nM 6.28
CHEMBL317734 IC50 = 1500.0 nM 5.82
CHEMBL98748 IC50 = 2300.0 nM 5.64
CHEMBL98 VORINOSTAT IC50 = 2400.0 nM 5.62
CHEMBL98428 IC50 = 14000.0 nM 4.85