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

CHEMBL5733800

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

Binding
Inhibition Assay: HDAC inhibition assays were performed by Reaction Biology Corp. (Malvern, Pa.) using isolated human, recombinant full-length HDAC1 and -6 from a baculovirus expression system in Sf9 cells. An acetylated fluorogenic peptide, RHKKAc, derived from residues 379-382 of p53 was used as substrate. The reaction buffer was made up of 50 mM Tris-HCl pH 8.0, 127 mM NaCl, 2.7 mM KCl, 1 mM MgCl2, 1 mg/mL BSA, and a final concentration of 1% DMSO. Compounds were delivered in DMSO and delivered to enzyme mixture with preincubation of 5-10 min followed by substrate addition and incubation for 2 h at 30° C. Trichostatin A and developer were added to quench the reaction and generate fluorescence, respectively. Dose-response curves were generated starting at 30 μM compound with three-fold serial dilutions to generate a 10-dose plot. IC50 values were then generated from the resulting plots, and the values expressed are the average of duplicate trials±standard deviation.
63
Total Activities
21
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 6 (CHEMBL1865)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Selective histone deactylase 6 inhibitors
(2018)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 21 7.74 8.92
kon 21 - -
k_off 21 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL185013 3 8.92
CHEMBL3914736 3 8.66
CHEMBL2179249 3 8.62
CHEMBL2179618 NEXTURASTAT A 3 8.30
CHEMBL2179615 3 8.24
CHEMBL3890261 3 8.16
CHEMBL6025821 3 8.08
CHEMBL2179617 3 8.03
CHEMBL2179616 3 7.93
CHEMBL2179619 3 7.85
CHEMBL2018302 TUBASTATIN A 3 7.82
CHEMBL5863042 3 7.65
CHEMBL2179244 3 7.60
CHEMBL3971359 3 7.59
CHEMBL2179246 3 7.39
CHEMBL2179245 3 7.22
CHEMBL3943331 3 7.13
CHEMBL2179247 3 6.86
CHEMBL2179248 3 6.34
CHEMBL2179250 3 6.33
CHEMBL272980 MOCETINOSTAT 2.0 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL185013 IC50 = 1.2 nM 8.92
CHEMBL3914736 IC50 = 2.2 nM 8.66
CHEMBL2179249 IC50 = 2.38 nM 8.62
CHEMBL2179618 NEXTURASTAT A IC50 = 5.02 nM 8.30
CHEMBL2179615 IC50 = 5.8 nM 8.24
CHEMBL3890261 IC50 = 6.9 nM 8.16
CHEMBL6025821 IC50 = 8.3 nM 8.08
CHEMBL2179617 IC50 = 9.26 nM 8.03
CHEMBL2179616 IC50 = 11.7 nM 7.93
CHEMBL2179619 IC50 = 14.0 nM 7.85
CHEMBL2018302 TUBASTATIN A IC50 = 15.0 nM 7.82
CHEMBL5863042 IC50 = 22.2 nM 7.65
CHEMBL2179244 IC50 = 25.2 nM 7.60
CHEMBL3971359 IC50 = 25.6 nM 7.59
CHEMBL2179246 IC50 = 41.1 nM 7.39
CHEMBL2179245 IC50 = 60.3 nM 7.22
CHEMBL3943331 IC50 = 74.2 nM 7.13
CHEMBL2179247 IC50 = 139.0 nM 6.86
CHEMBL2179248 IC50 = 458.0 nM 6.34
CHEMBL2179250 IC50 = 468.0 nM 6.33
CHEMBL5863042 k_off = - s-1 -
CHEMBL3971359 kon = - -
CHEMBL3971359 k_off = - s-1 -
CHEMBL2179617 kon = - -
CHEMBL2179247 kon = - -
CHEMBL2179247 k_off = - s-1 -
CHEMBL2179248 kon = - -
CHEMBL2179248 k_off = - s-1 -
CHEMBL2179249 kon = - -
CHEMBL2179249 k_off = - s-1 -
CHEMBL2179250 kon = - -
CHEMBL2179250 k_off = - s-1 -
CHEMBL2179615 kon = - -
CHEMBL2179615 k_off = - s-1 -
CHEMBL2179616 kon = - -
CHEMBL5863042 kon = - -
CHEMBL3943331 k_off = - s-1 -
CHEMBL3943331 kon = - -
CHEMBL272980 MOCETINOSTAT k_off = - s-1 -
CHEMBL272980 MOCETINOSTAT kon = - -
CHEMBL272980 MOCETINOSTAT IC50 > 10000.0 nM -
CHEMBL2179245 kon = - -
CHEMBL185013 kon = - -
CHEMBL2018302 TUBASTATIN A k_off = - s-1 -
CHEMBL2018302 TUBASTATIN A kon = - -
CHEMBL3914736 kon = - -
CHEMBL3890261 k_off = - s-1 -
CHEMBL3914736 k_off = - s-1 -
CHEMBL3890261 kon = - -
CHEMBL185013 k_off = - s-1 -