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Inhibition of BRD3-BD2 (unknown origin) assessed as dissociation constant by TR-FRET method
Assay data:2 Active, 2 Activity ≤ 1 µM, 2 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of BRD3-BD1 (unknown origin) assessed as dissociation constant by TR-FRET method
Assay data:2 Active, 2 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
LPS-PBMC assay (MCP-1)
Assay data:1 Active, 1 Activity ≤ 1 µM, 1 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMRelated BioAssays by Target
In vitro inhibition of MCP-1 in Lipopolysaccharide-stimulated human whole blood
BRD4 BD2 SPR
BRDT BD2 Bromoscan (DiscoverX)
BRD4 BD2 Bromoscan (DiscoverX)
BRD3 BD2 Bromoscan (DiscoverX)
BRD2 BD2 Bromoscan (DiscoverX)
BET mutant TR-FRET assay (BRDT BD2)
BET mutant TR-FRET assay (BRD4 BD2)
BET mutant TR-FRET assay (BRD3 BD2)
BET mutant TR-FRET assay (BRD2 BD2)
TR-FRET assay (BRDT BD2)
Assay data:2 Active, 2 Activity ≤ 1 µM, 3 Tested
TR-FRET assay (BRD4 BD2)
TR-FRET assay (BRD3 BD2)
TR-FRET assay (BRD2 BD2)
Inhibition of 6His-Thr-BRD4 (1 to 477 residues) BD1 domain (unknown origin) incubated for 30 mins by TR-FRET assay
Assay data:11 Active, 2 Activity ≤ 1 µM, 40 Tested
Binding affinity to 6His-Thr-BRD4 (1 to 477 residues) BD2 domain Y390A mutant (unknown origin) incubated for 30 mins by TR-FRET assay
Assay data:48 Active, 47 Activity ≤ 1 µM, 49 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed Citation
Inhibition of 6His-Thr-BRD4 (1 to 477 residues) BD2 domain Y390A mutant (unknown origin) incubated for 30 mins by TR-FRET assay
Assay data:48 Active, 41 Activity ≤ 1 µM, 51 Tested
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