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Assay Detail

CHEMBL895787

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

Binding
Inhibition of HDAC in HeLa cells
16
Total Activities
16
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Cell Type HeLa
Confidence 5 — Multiple protein complex / RNA
Curated By Autocuration

Target

Histone deacetylase (CHEMBL2093865)
Type PROTEIN FAMILY
Organism Homo sapiens

Publication

2-aroylindoles and 2-aroylbenzofurans with N-hydroxyacrylamide substructures as a novel series of rationally designed histone deacetylase inhibitors.
Mahboobi S, Sellmer A, Höcher H, Garhammer C, Pongratz H, Maier T, Ciossek T, Beckers T.
J Med Chem (2007) 50 : 4405 -4418
PubMed 17691763 · DOI

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 16 6.69 7.47

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL390907 1 7.47
CHEMBL242533 1 7.41
CHEMBL390452 1 7.24
CHEMBL98 VORINOSTAT 4.0 1 7.16
CHEMBL388429 1 7.05
CHEMBL390910 1 6.92
CHEMBL244040 1 6.58
CHEMBL243181 1 6.57
CHEMBL396559 1 6.55
CHEMBL390908 1 6.51
CHEMBL244885 1 6.48
CHEMBL244670 1 6.47
CHEMBL243809 1 6.35
CHEMBL244887 1 6.19
CHEMBL397904 1 6.08
CHEMBL395976 1 6.00

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL390907 IC50 = 34.0 nM 7.47
CHEMBL242533 IC50 = 39.0 nM 7.41
CHEMBL390452 IC50 = 57.0 nM 7.24
CHEMBL98 VORINOSTAT IC50 = 70.0 nM 7.16
CHEMBL388429 IC50 = 90.0 nM 7.05
CHEMBL390910 IC50 = 120.0 nM 6.92
CHEMBL244040 IC50 = 260.0 nM 6.58
CHEMBL243181 IC50 = 270.0 nM 6.57
CHEMBL396559 IC50 = 280.0 nM 6.55
CHEMBL390908 IC50 = 310.0 nM 6.51
CHEMBL244885 IC50 = 330.0 nM 6.48
CHEMBL244670 IC50 = 340.0 nM 6.47
CHEMBL243809 IC50 = 450.0 nM 6.35
CHEMBL244887 IC50 = 650.0 nM 6.19
CHEMBL397904 IC50 = 830.0 nM 6.08
CHEMBL395976 IC50 = 1000.0 nM 6.00