BDBM178100 BRD3308::US11377423, Cmpd 1

SMILES CC(=O)Nc1ccc(cc1)C(=O)Nc1ccc(F)cc1N

InChI Key InChIKey=RRJDFENBXIEAPD-UHFFFAOYSA-N

Data  6 KI  46 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 49 hits for monomerid = 178100   

TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.15E+3nMAssay Description:Inhibition of human HDAC2 measured after 1 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.08E+3nMAssay Description:Inhibition of human recombinant HDAC1 at 0.1 uM using AMC-K(Ac)GL as substrate incubated for 60 mins by fluorescence based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2024
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.25E+3nMAssay Description:The following non-trypsin coupled in-vitro HDAC enzymatic endpoint assay was used to assay the compounds of the invention. Below is a standardized pr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/5/2022
Entry Details
Go to US Patent

TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.42E+3nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/5/2022
Entry Details
Go to US Patent

TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 68nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/5/2022
Entry Details
Go to US Patent

TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.25E+3nMAssay Description:The following non-trypsin coupled in-vitro HDAC enzymatic endpoint assay was used to assay the compounds of the invention. Below is a standardized pr...More data for this Ligand-Target Pair
In Depth
Date in BDB:
10/5/2022
Entry Details
Go to US Patent

TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.42E+3nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/5/2022
Entry Details
Go to US Patent

TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 68nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
10/5/2022
Entry Details
Go to US Patent

TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.26E+3nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.34E+3nMAssay Description:Inhibition of HDAC2 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 54nMAssay Description:Inhibition of HDAC3 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/17/2024
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.08E+3nMAssay Description:Inhibition of human HDAC1 measured after 1 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.15E+3nMAssay Description:Inhibition of human recombinant HDAC2 at 0.1 uM using AMC-K(Ac)GL as substrate incubated for 60 mins by fluorescence based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2024
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 64nMAssay Description:Inhibition of human HDAC3 measured after 1 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 2.19E+3nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.51E+3nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 61nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 4(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 5(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 6(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 7(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 8(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 9(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/4/2025
Entry Details
Go to US Patent

TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 64nMAssay Description:Inhibition of human recombinant HDAC3 at 0.5 uM using AMC-K(Ac)GL as substrate incubated for 60 mins by fluorescence based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/19/2024
Entry Details
PubMed
TargetHistone deacetylase 5(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.33E+4nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.33E+4nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 7(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.33E+4nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 8(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.33E+4nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 9(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.33E+4nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 64nMAssay Description:Inhibition of HDAC3 (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/19/2020
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.15E+3nMAssay Description:Inhibition of recombinant human full length C-terminal FLAG-tagged HDAC2 expressed in Sf9 insect cells using FAM-labeled acetylated peptide A as subs...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.08E+3nMAssay Description:Inhibition of recombinant human full length C-terminal His/FALG-tagged HDAC1 expressed in Sf9 insect cells using FAM-labeled acetylated peptide A as ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 64nMAssay Description:Inhibition of recombinant human full length HDAC3 using FAM-labeled acetylated peptide A as substrate preincubated for 3 hrs followed by substrate ad...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/25/2021
Entry Details Article
PubMed
TargetHistone deacetylase 4(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.33E+4nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of HDAC1 (unknown origin) using carboxyfluorescein (FAM)-labeled acetylated peptide substrate preincubated for 3 hrs by microfluidic capil...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human HDAC2 expressed in Sf9 cells using carboxyfluorescein (FAM)-labeled acetylated peptide substrate preincubated for 3 hrs by microf...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)(Human)
University of East Anglia

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 64nMAssay Description:Inhibition of His-tagged GST-fused human HDAC3/NcoR2 expressed in sf9 cells using carboxyfluorescein (FAM)-labeled acetylated peptide substrate prein...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 4(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human HDAC4 expressed in baculovirus infected sf9 cells using carboxyfluorescein (FAM)-labeled acetylated peptide substrate by microflu...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 5(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human HDAC5 using carboxyfluorescein (FAM)-labeled acetylated peptide substrate by microfluidic capillary electrophoresisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of HDAC6 (unknown origin) using carboxyfluorescein (FAM)-labeled acetylated peptide substrate by microfluidic capillary electrophoresisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 7(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human N-terminal GST-tagged HDAC7 (518 to end residues) expressed in baculovirus infected sf9 cells using carboxyfluorescein (FAM)-labe...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 8(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of recombinant human C-terminal His-tagged HDAC8 expressed in baculovirus infected sf9 cells using carboxyfluorescein (FAM)-labeled acetyl...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 9(Human)
Kdac Therapeutics

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of C-terminal His-tagged human HDAC9 (604 to 1066 residues) expressed in baculovirus infected sf9 cells using carboxyfluorescein (FAM)-lab...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/29/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataKi:  29nM ΔG°:  -10.3kcal/mole IC50: 64nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
The Broad Institute

US Patent
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataKi:  29nMAssay Description:Binding affinity to human HDAC3 assessed as inhibition constant measured after 1 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataKi:  5.10E+3nM ΔG°:  -7.21kcal/mole IC50: 1.08E+3nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Jadavpur University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataKi:  5.10E+3nMAssay Description:Binding affinity to human HDAC1 assessed as inhibition constant measured after 1 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataKi:  6.30E+3nMAssay Description:Binding affinity to human HDAC2 assessed as inhibition constant measured after 1 hrsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/14/2024
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
Osaka University

Curated by ChEMBL
LigandPNGBDBM178100(BRD3308 | US11377423, Cmpd 1)
Affinity DataKi:  6.30E+3nM ΔG°:  -7.09kcal/mole IC50: 1.15E+3nMpH: 7.4 T: 2°CAssay Description:Purified HDAC1-9 (0.5~5 nM) were incubated with 2 μM carboxyfluorescein (FAM)-labeled acetylated peptide substrate A or B and test compound for ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
5/2/2016
Entry Details Article
PubMed