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Assay Detail

CHEMBL5730140

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

Binding
Enzyme Assay: The assay has been carried out in 96 well format and the BIOMOL fluorescent-based HDAC activity assay has been applied. The reaction composed of assay buffer, containing 25 mM Tris pH 7.5, 137 mM NaCl, 2.7 mM KCl, 1 mM MgCl2, 1 mg/ml BSA, tested compounds, 500 nM HDAC8 enzyme or 600 nM HDAC1 enzyme, 200 μM Flur de lys p53 peptide substrate for HDAC8 enzyme or 500 μM Flur de lys generic substrate for HDAC1 enzyme and subsequently was incubated at room temperature for 2 h. Flur de lys Developer was added and the reaction was incubated for 10 min. Briefly, deacetylation of the substrate sensitizes it to the developer, which then generates a fluorophore (symbol). The fluorophore is excited with 360 nm light and the emitted light (460 nm) is detected on a fluorometric plate reader.
288
Total Activities
96
Compounds Tested
3
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 1 (CHEMBL325)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Benzimidazole derivatives: preparation and pharmaceutical applications
(2020)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 96 6.46 7.62
kon 96 - -
k_off 96 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL460963 3 7.62
CHEMBL491688 3 7.58
CHEMBL3648287 3 7.52
CHEMBL489332 3 7.41
CHEMBL474746 3 7.29
CHEMBL3648290 3 7.28
CHEMBL491316 3 7.28
CHEMBL3648280 3 7.27
CHEMBL3648291 3 7.21
CHEMBL3648305 3 7.21
CHEMBL3648289 3 7.19
CHEMBL475145 3 7.19
CHEMBL3648279 3 7.15
CHEMBL491491 3 7.14
CHEMBL3648267 3 7.04
CHEMBL5811849 3 7.00
CHEMBL3648306 3 6.94
CHEMBL3648285 3 6.94
CHEMBL3648292 3 6.90
CHEMBL3645375 3 6.88
CHEMBL3648281 3 6.88
CHEMBL5907207 3 6.86
CHEMBL3648308 3 6.84
CHEMBL474349 3 6.82
CHEMBL523601 3 6.80
CHEMBL5906708 3 6.80
CHEMBL489331 3 6.79
CHEMBL3648286 3 6.78
CHEMBL3648288 3 6.78
CHEMBL442585 3 6.78

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL460963 IC50 = 24.0 nM 7.62
CHEMBL491688 IC50 = 26.0 nM 7.58
CHEMBL3648287 IC50 = 30.0 nM 7.52
CHEMBL489332 IC50 = 39.0 nM 7.41
CHEMBL474746 IC50 = 51.0 nM 7.29
CHEMBL3648290 IC50 = 52.0 nM 7.28
CHEMBL491316 IC50 = 52.0 nM 7.28
CHEMBL3648280 IC50 = 54.0 nM 7.27
CHEMBL3648305 IC50 = 62.0 nM 7.21
CHEMBL3648291 IC50 = 61.0 nM 7.21
CHEMBL475145 IC50 = 64.0 nM 7.19
CHEMBL3648289 IC50 = 65.0 nM 7.19
CHEMBL3648279 IC50 = 71.0 nM 7.15
CHEMBL491491 IC50 = 72.0 nM 7.14
CHEMBL3648267 IC50 = 92.0 nM 7.04
CHEMBL5811849 IC50 = 100.0 nM 7.00
CHEMBL3648285 IC50 = 116.0 nM 6.94
CHEMBL3648306 IC50 = 116.0 nM 6.94
CHEMBL3648292 IC50 = 125.0 nM 6.90
CHEMBL3645375 IC50 = 131.0 nM 6.88
CHEMBL3648281 IC50 = 131.0 nM 6.88
CHEMBL5907207 IC50 = 137.0 nM 6.86
CHEMBL3648308 IC50 = 146.0 nM 6.84
CHEMBL474349 IC50 = 153.0 nM 6.82
CHEMBL5906708 IC50 = 160.0 nM 6.80
CHEMBL523601 IC50 = 158.0 nM 6.80
CHEMBL489331 IC50 = 162.0 nM 6.79
CHEMBL3648312 IC50 = 167.0 nM 6.78
CHEMBL464719 IC50 = 167.0 nM 6.78
CHEMBL442585 IC50 = 165.0 nM 6.78
CHEMBL3648288 IC50 = 168.0 nM 6.78
CHEMBL3648286 IC50 = 166.0 nM 6.78
CHEMBL474152 IC50 = 171.0 nM 6.77
CHEMBL515906 IC50 = 173.0 nM 6.76
CHEMBL489706 IC50 = 194.0 nM 6.71
CHEMBL3648316 IC50 = 196.0 nM 6.71
CHEMBL523646 IC50 = 195.0 nM 6.71
CHEMBL1377382 IC50 = 195.0 nM 6.71
CHEMBL3648268 IC50 = 206.0 nM 6.69
CHEMBL521909 IC50 = 206.0 nM 6.69
CHEMBL490721 IC50 = 218.0 nM 6.66
CHEMBL489125 IC50 = 227.0 nM 6.64
CHEMBL6030983 IC50 = 230.0 nM 6.64
CHEMBL3648318 IC50 = 234.0 nM 6.63
CHEMBL491490 IC50 = 246.0 nM 6.61
CHEMBL489709 IC50 = 268.0 nM 6.57
CHEMBL5907529 IC50 = 290.0 nM 6.54
CHEMBL3645371 IC50 = 286.0 nM 6.54
CHEMBL3648294 IC50 = 294.0 nM 6.53
CHEMBL3648284 IC50 = 297.0 nM 6.53