Compile Data Set for Download or QSAR
Report error Found 69 Enz. Inhib. hit(s) with all data for entry = 11940
TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663026BDBM663026(N-(6-((1H-pyrazol-1-yl)methyl)-4-(fluoromethoxy)be...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663029BDBM663029(N-(6-((1H-pyrazol-1-yl)methyl)-4-(fluoromethoxy)be...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663023BDBM663023(N-(6-((1H-pyrazol-1-yl)methyl)-4-(fluoromethoxy) b...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663022BDBM663022(2,6-dimethoxy-N-(5-(pyridin-2-ylmethyl)-3,4-dihydr...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663035BDBM663035(2-methoxy-N-(4-methoxy-6-(thiazol-2-yloxy)benzo[d]...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663034BDBM663034(2,6-dimethoxy-N-(4-methoxy-6-(thiazol-2-yloxy)benz...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663037BDBM663037(2,6-dimethoxy-N-(6-(thiazol-2-yloxy)-2,3,4,5,9,10-...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663036BDBM663036(2-methoxy-N-(5-(thiazol-2-yloxy)-3,4-dihydro-2H-ch...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663031BDBM663031(N-(4-(fluoromethoxy)-6-(thiazol-2-yloxy)benzo[d]is...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663033BDBM663033(N-(6-((1H-pyrazol-1-yl)methyl)-4-(fluoromethoxy)be...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663032BDBM663032(2,4-dimethoxy-N-(4-methoxy-6-(thiazol-2-yloxy)benz...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663011BDBM663011(2,6-dimethoxy-N-(5-((3-methylpyridin-2-yl)oxy)-3,4...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663010BDBM663010(2,6-dimethoxy-N-(5-(thiazol-2-yloxy)-3,4-dihydro-2...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663012BDBM663012(N-(4-(fluoromethoxy)-6-(pyridin-2-ylmethyl)benzo[d...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663006BDBM663006(N-(6-((1H-pyrazol-1-yl)methyl)-4-(fluoromethoxy)be...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663009BDBM663009(2,6-dimethoxy-N-(5-(oxazol-2-yloxy)-3,4-dihydro-2H...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663021BDBM663021(2,6-dimethoxy-N-(5-(pyridin-2-ylmethyl)-3,4-dihydr...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662995BDBM662995(N-(6-((1H-pyrazol-1-yl)methyl)-2,3,4,5-tetrahydroo...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662994BDBM662994(N-(6-((1H-pyrazol-1-yl)methyl)-2,3,4,5,9,10-hexahy...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662996BDBM662996(N-(6-((1H-pyrazol-1-yl)methyl)-2,3,4,5-tetrahydroo...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662990BDBM662990(N-(5-((1H-pyrazol-1-yl)methyl)-3,4-dihydro-2H-chro...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662993BDBM662993(N-(5-((1H-pyrazol-1-yl)methyl)-3,4-dihydro-2H-chro...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662992BDBM662992(N-(5-((1H-pyrazol-1-yl)methyl)-3,4-dihydro-2H-chro...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662999BDBM662999(2,6-dimethoxy-N-(5-(pyridin-2-yloxy)-3,4-dihydro-2...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662998BDBM662998(2,6-dimethoxy-N-(4-(pyridin-2-yloxy)-2,3-dihydrobe...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663000BDBM663000(2-methoxy-N-(5-(pyridin-2-yloxy)-3,4-dihydro-2H-ch...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662978BDBM662978(N-(6-((1H-pyrazol-1-yl)methyl)-4-(difluoromethoxy)...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663044BDBM663044(N-(7-((1H-pyrazol-1-yl)methyl)-5,5a,6,6a-tetrahydr...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663039BDBM663039(2,4-dimethoxy-6-methyl-N-(6-(thiazol-2-yloxy)-2,3,...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663038BDBM663038(2-methoxy-N-(6-(thiazol-2-yloxy)-2,3,4,5,9,10-hexa...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663041BDBM663041(2,6-dimethoxy-N-(4-methoxy-6-(thiazol-2-ylthio)ben...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663040BDBM663040(N-(4-(fluoromethoxy)-6-(thiazol-2-ylmethyl)benzo[d...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662986BDBM662986(N-(6-((1H-pyrazol-1-yl)methyl)-4-methoxybenzo[d]is...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662989BDBM662989(N-(5-((1H-pyrazol-1-yl)methyl)-3,4-dihydro-2H-chro...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662985BDBM662985(7-chloro-1-(2-chlorophenyl)-4-(prop-2-yn-1-ylamino...)
Affinity DataIC50: 5nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663027BDBM663027(US20240109880, Compound 52)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663028BDBM663028(N-(6-((1H-pyrazol-1-yl)methyl)-4-(fluoromethoxy)be...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663024BDBM663024(N-(6-((1H-pyrazol-1-yl)methyl)-4-(fluoromethoxy)be...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663030BDBM663030(N-(4-(fluoromethoxy)-6-(thiazol-2-yloxy)benzo[d]is...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663007BDBM663007(N-(4-((1H-pyrazol-1-yl)methyl)-2,3-dihydrobenzofur...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663008BDBM663008(2,6-dimethoxy-N-(5-(pyrimidin-2-yloxy)-3,4-dihydro...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663019BDBM663019(N-(6-((1H-pyrazol-1-yl)methyl)-4-(difluoromethoxy)...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663018BDBM663018(N-(6-((1H-pyrazol-1-yl)methyl)-5-fluoro-4-(fluorom...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663020BDBM663020(N-(4-(fluoromethoxy)-6-(pyridin-2-ylmethyl)benzo[d...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663014BDBM663014(N-(6-((1H-pyrazol-1-yl)methyl)-4-methoxybenzo[d]is...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663017BDBM663017(N-(6-((1H-pyrazol-1-yl)methyl)-5-fluoro-4-(fluorom...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663016BDBM663016(N-(6-((1H-pyrazol-1-yl)methyl)-4-methoxybenzo[d]is...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662997BDBM662997(N-(4-(difluoromethoxy)-6-(pyridin-2-yloxy)benzo[d]...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 662991BDBM662991(N-(5-((1H-pyrazol-1-yl)methyl)-3,4-dihydro-2H-chro...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

TargetHistone acetyltransferase KAT6A [507-778](Human)
Insilico Medicine IP

US Patent
LigandChemical structure of BindingDB Monomer ID 663003BDBM663003(2,4-dimethoxy-N-(5-(pyridin-2-yloxy)-3,4-dihydro-2...)
Affinity DataIC50: 55nMAssay Description:Inhibition of KAT6A enzymatic activity by test compounds was determined using a radiometric 384-well format assay. A 10-point serial dilution of the ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/20/2024
Entry Details
US Patent

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