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Assay Detail

CHEMBL3707557

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

Binding
Enzyme Assay: Compounds for testing were diluted in DMSO to 50 fold the final concentration and a ten point three fold dilution series was made. The compounds were diluted in assay buffer (50 mM HEPES, pH 7.4, 100 mM KCl, 0.001% Tween-20, 0.05% BSA, 20 uM TCEP) to 6 fold their final concentration. The HDAC enzymes (purchased from BPS Biosciences) were diluted to 1.5 fold their final concentration in assay buffer. The tripeptide substrate and trypsin at 0.05 uM final concentration were diluted in assay buffer at 6 fold their final concentration. The final enzyme concentrations used in these assays were 3.3 ng/ml (HDAC1), 0.2 ng/ml (HDAC2), 0.08 ng/ml (HDAC3) and 2 ng/ml (HDAC6). The final substrate concentrations used were 16 uM (HDAC1), 10 uM (HDAC2), 17 uM (HDAC3) and 14 uM (HDAC6). Five ul of compounds and 20 ul of enzyme were added to wells of a black, opaque 384 well plate in duplicate. Enzyme and compound were incubated together at room temperature.
140
Total Activities
137
Compounds Tested
1
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Organism Homo sapiens
Confidence 9 — Direct single protein target
Curated By Autocuration

Target

Histone deacetylase 2 (CHEMBL1937)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Pyrimidine hydroxy amide compounds as protein deacetylase inhibitors and methods of use thereof
(2013)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 140 6.63 8.22

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL3655993 1 8.22
CHEMBL3655984 1 8.05
CHEMBL3655995 1 8.05
CHEMBL3655992 1 7.92
CHEMBL3656012 1 7.77
CHEMBL3656010 1 7.77
CHEMBL3655997 1 7.77
CHEMBL3655959 1 7.75
CHEMBL3655994 1 7.72
CHEMBL3656000 1 7.72
CHEMBL3655979 1 7.68
CHEMBL3656006 1 7.68
CHEMBL3656015 1 7.66
CHEMBL3656011 1 7.64
CHEMBL3655974 1 7.55
CHEMBL3655917 1 7.55
CHEMBL3655936 1 7.52
CHEMBL3655990 1 7.50
CHEMBL3655971 1 7.50
CHEMBL3656013 1 7.47
CHEMBL3655967 1 7.44
CHEMBL3655944 2 7.41
CHEMBL3656005 1 7.40
CHEMBL3656003 1 7.40
CHEMBL3656007 1 7.31
CHEMBL3655929 1 7.28
CHEMBL3655989 1 7.28
CHEMBL3655998 1 7.28
CHEMBL3655923 1 7.25
CHEMBL3655996 1 7.24

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL3655993 IC50 = 6.0 nM 8.22
CHEMBL3655984 IC50 = 9.0 nM 8.05
CHEMBL3655995 IC50 = 9.0 nM 8.05
CHEMBL3655992 IC50 = 12.0 nM 7.92
CHEMBL3656010 IC50 = 17.0 nM 7.77
CHEMBL3655997 IC50 = 17.0 nM 7.77
CHEMBL3656012 IC50 = 17.0 nM 7.77
CHEMBL3655959 IC50 = 18.0 nM 7.75
CHEMBL3655994 IC50 = 19.0 nM 7.72
CHEMBL3656000 IC50 = 19.0 nM 7.72
CHEMBL3656006 IC50 = 21.0 nM 7.68
CHEMBL3655979 IC50 = 21.0 nM 7.68
CHEMBL3656015 IC50 = 22.0 nM 7.66
CHEMBL3656011 IC50 = 23.0 nM 7.64
CHEMBL3655917 IC50 = 28.0 nM 7.55
CHEMBL3655974 IC50 = 28.0 nM 7.55
CHEMBL3655936 IC50 = 30.0 nM 7.52
CHEMBL3655971 IC50 = 32.0 nM 7.50
CHEMBL3655990 IC50 = 32.0 nM 7.50
CHEMBL3656013 IC50 = 34.0 nM 7.47
CHEMBL3655967 IC50 = 36.0 nM 7.44
CHEMBL3655944 IC50 = 39.0 nM 7.41
CHEMBL3656003 IC50 = 40.0 nM 7.40
CHEMBL3656005 IC50 = 40.0 nM 7.40
CHEMBL3656007 IC50 = 49.0 nM 7.31
CHEMBL3655998 IC50 = 52.0 nM 7.28
CHEMBL3655989 IC50 = 53.0 nM 7.28
CHEMBL3655929 IC50 = 53.0 nM 7.28
CHEMBL3655923 IC50 = 56.0 nM 7.25
CHEMBL3655944 IC50 = 56.0 nM 7.25
CHEMBL3655996 IC50 = 57.0 nM 7.24
CHEMBL3656009 IC50 = 62.0 nM 7.21
CHEMBL3655919 IC50 = 71.0 nM 7.15
CHEMBL3656016 IC50 = 73.0 nM 7.14
CHEMBL3655958 IC50 = 78.0 nM 7.11
CHEMBL3655915 IC50 = 79.0 nM 7.10
CHEMBL3652232 IC50 = 82.0 nM 7.09
CHEMBL3655915 IC50 = 83.0 nM 7.08
CHEMBL3655962 IC50 = 96.0 nM 7.02
CHEMBL3656001 IC50 = 96.0 nM 7.02
CHEMBL3655925 IC50 = 97.0 nM 7.01
CHEMBL3655970 IC50 = 107.0 nM 6.97
CHEMBL3655964 IC50 = 116.0 nM 6.94
CHEMBL3656004 IC50 = 118.0 nM 6.93
CHEMBL3655926 IC50 = 120.0 nM 6.92
CHEMBL3655957 IC50 = 127.0 nM 6.90
CHEMBL3655920 IC50 = 127.0 nM 6.90
CHEMBL3655950 IC50 = 128.0 nM 6.89
CHEMBL3655983 IC50 = 133.0 nM 6.88
CHEMBL3656014 IC50 = 135.0 nM 6.87