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

CHEMBL5731984

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

Binding
Binding Assay: BRD binding and inhibition was assessed by measuring the interaction of biotinylated acetyl-histone H4 peptide (Anaspec #64989) with the BRD target protein utilising AlphaScreen® technology (Perkin Elmer). In a white 384-well low volume plate (Greiner #784076), 100 nL of compound series in DMSO (0.5% final concentration) was added to the BRD target protein (80 nM final). After 30 min incubation at RT, H4 peptide was added to a final concentration of 2.5 nM. AlphaScreen streptavidin donor beads and AlphaScreen nickel chelate acceptor beads were added to a final concentration of 10 ug/mL each and allowed to incubate in a darkened environment for 1 h at RT. Plates were read on an EnVision plate reader (Perkin Elmer) and IC50's calculated using a four parameter non-linear curve fit.These conditions are identical for all BRDs screened except BRD2D2 which uses 160 nM protein and 1.25 nM peptide.
72
Total Activities
24
Compounds Tested
3
Activity Types
0
Assay Parameters

Assay Information

Assay Type Binding
Confidence 8 — Homologous single protein target
Curated By Autocuration

Target

Bromodomain-containing protein 3 (CHEMBL1795186)
Type SINGLE PROTEIN
Organism Homo sapiens

Publication

Benzodiazepines as bromodomain inhibitors
(2019)

Activity Statistics

Type Count Avg pChEMBL Best pChEMBL
IC50 24 6.26 6.26
kon 24 - -
k_off 24 - -

Compounds Tested

Compound Name Phase Activities Best pChEMBL
CHEMBL5877617 3 6.26
CHEMBL4164698 3 -
CHEMBL4173305 3 -
CHEMBL4168815 3 -
CHEMBL4177080 3 -
CHEMBL4169877 3 -
CHEMBL4176672 3 -
CHEMBL4159455 3 -
CHEMBL4170756 3 -
CHEMBL4161952 3 -
CHEMBL4162818 3 -
CHEMBL5750073 3 -
CHEMBL5981954 3 -
CHEMBL4174764 3 -
CHEMBL4166861 3 -
CHEMBL4173537 3 -
CHEMBL4166455 3 -
CHEMBL4162832 3 -
CHEMBL4169698 3 -
CHEMBL4166286 3 -
CHEMBL4166671 3 -
CHEMBL4176902 3 -
CHEMBL4174587 3 -
CHEMBL5878227 3 -

Activity Data

Compound Name Type Rel. Value Units pChEMBL
CHEMBL5877617 IC50 = 550.0 nM 6.26
CHEMBL4176672 k_off = - s-1 -
CHEMBL4166671 kon = - -
CHEMBL5878227 IC50 < 100.0 nM -
CHEMBL4166286 k_off = - s-1 -
CHEMBL4166286 kon = - -
CHEMBL4166286 IC50 < 100.0 nM -
CHEMBL4169698 k_off = - s-1 -
CHEMBL4169698 kon = - -
CHEMBL4169698 IC50 < 100.0 nM -
CHEMBL4162832 k_off = - s-1 -
CHEMBL4162832 kon = - -
CHEMBL4177080 IC50 < 100.0 nM -
CHEMBL4166671 k_off = - s-1 -
CHEMBL4176672 kon = - -
CHEMBL4176672 IC50 < 100.0 nM -
CHEMBL4169877 k_off = - s-1 -
CHEMBL4169877 kon = - -
CHEMBL4169877 IC50 < 100.0 nM -
CHEMBL4177080 k_off = - s-1 -
CHEMBL4177080 kon = - -
CHEMBL4159455 IC50 < 100.0 nM -
CHEMBL4168815 k_off = - s-1 -
CHEMBL4168815 kon = - -
CHEMBL4168815 IC50 < 100.0 nM -
CHEMBL4173305 k_off = - s-1 -
CHEMBL4174764 kon = - -
CHEMBL4166861 IC50 < 100.0 nM -
CHEMBL4166455 k_off = - s-1 -
CHEMBL4166455 kon = - -
CHEMBL4166455 IC50 < 100.0 nM -
CHEMBL4173537 k_off = - s-1 -
CHEMBL4173537 kon = - -
CHEMBL4173537 IC50 < 100.0 nM -
CHEMBL4166861 k_off = - s-1 -
CHEMBL4166861 kon = - -
CHEMBL4162832 IC50 < 100.0 nM -
CHEMBL4174764 k_off = - s-1 -
CHEMBL4176902 IC50 < 100.0 nM -
CHEMBL4174764 IC50 < 100.0 nM -
CHEMBL5877617 k_off = - s-1 -
CHEMBL5877617 kon = - -
CHEMBL5878227 k_off = - s-1 -
CHEMBL5878227 kon = - -
CHEMBL4166671 IC50 < 100.0 nM -
CHEMBL4174587 k_off = - s-1 -
CHEMBL4174587 kon = - -
CHEMBL4174587 IC50 < 100.0 nM -
CHEMBL4176902 k_off = - s-1 -
CHEMBL4176902 kon = - -