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Found 1960 with Last Name = 'keung' and Initial = 'w'
TargetAldehyde dehydrogenase, mitochondrial(Homo sapiens (Human))
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50359990(PRUNETIN)
Affinity DataKi:  450nMAssay Description:Inhibition of human recombinant ALDH2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Takeda California

Curated by ChEMBL
LigandPNGBDBM50234304(CHEMBL4062894)
Affinity DataIC50:  1nMAssay Description:Inhibition of Axl (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Takeda California

Curated by ChEMBL
LigandPNGBDBM50234305(CHEMBL4090103)
Affinity DataIC50:  1.80nMAssay Description:Inhibition of Axl (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Takeda California

Curated by ChEMBL
LigandPNGBDBM50234306(CHEMBL4094158)
Affinity DataIC50:  2.20nMAssay Description:Inhibition of Axl (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397684((S)-N-(5-(6-cyano-5-((1-((2,2-difluoroethyl)(methy...)
Affinity DataIC50:  2.51nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAldehyde dehydrogenase, mitochondrial(Homo sapiens (Human))
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50093535(11-(3-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yloxy)u...)
Affinity DataIC50:  3nMAssay Description:Inhibition of Hamster Liver mitochondrial ALDH-2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397657((R)-N-(5-(4-cyano-3-((1-(dimethylamino)-1-oxobutan...)
Affinity DataIC50:  3.16nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Takeda California

Curated by ChEMBL
LigandPNGBDBM50234303(CHEMBL4066616)
Affinity DataIC50:  3.40nMAssay Description:Inhibition of Axl (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397717(N-(5-(6-cyano-5-(((S)-1-((2,2-difluoroethyl)(methy...)
Affinity DataIC50:  3.98nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetAldehyde dehydrogenase, mitochondrial(Homo sapiens (Human))
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50093537(10-(3-(4-hydroxyphenyl)-4-oxo-4H-chromen-7-yloxy)d...)
Affinity DataIC50:  4nMAssay Description:Inhibition of Hamster Liver mitochondrial ALDH-2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397772((R)-N-(5-(6-cyano-5-((2-(2-(difluoromethyl)pyrroli...)
Affinity DataIC50:  5.01nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397665((S)-N-(5-(4-cyano-3-((1-(dimethylamino)-4,4-difluo...)
Affinity DataIC50:  6.31nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397679((R)-N-(5-(6-cyano-5-((2-oxo-2-(2-(trifluoromethyl)...)
Affinity DataIC50:  6.31nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397638((S)-N-(5-(4-cyano-3-((1-(dimethylamino)-4-methoxy-...)
Affinity DataIC50:  6.31nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397750(N-(5-(6-cyano-5-(((2S)-1-((1,1-difluoropropan-2-yl...)
Affinity DataIC50:  7.94nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397777(N-(5-(6-cyano-5-(((S)-1-((2,2-difluoroethyl)(methy...)
Affinity DataIC50:  7.94nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397639(US9994547, Example 8.0)
Affinity DataIC50:  7.94nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397637(N-(5-(4-cyano-3-((1-(dimethylamino)-1-oxobutan-2-y...)
Affinity DataIC50:  7.94nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397632((S)-N-(5-(4-cyano-3-((1-(dimethylamino)-1-oxopropa...)
Affinity DataIC50:  7.94nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetAldehyde dehydrogenase, mitochondrial(Homo sapiens (Human))
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50093534(7-[3-(4-Hydroxy-phenyl)-4-oxo-4H-chromen-7-yloxy]-...)
Affinity DataIC50:  9nMAssay Description:Inhibition of Hamster Liver mitochondrial ALDH-2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldehyde dehydrogenase, mitochondrial(Homo sapiens (Human))
University Of Oxford

Curated by ChEMBL
LigandPNGBDBM50093531(6-[3-(4-Hydroxy-phenyl)-4-oxo-4H-chromen-7-yloxy]-...)
Affinity DataIC50:  9nMAssay Description:Inhibition of Hamster Liver mitochondrial ALDH-2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397643((S)-N-(5-(4-cyano-3-((1-(ethyl(methyl)amino)-1-oxo...)
Affinity DataIC50:  10nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397677(N-(5-(6-cyano-5-((1-((2,2-difluoroethyl)(methyl)am...)
Affinity DataIC50:  10nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397685((S)-N-(5-(6-cyano-5-((1-((2-fluoroethyl)(methyl)am...)
Affinity DataIC50:  10nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397634(US9994547, Example 3.0)
Affinity DataIC50:  12.6nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397720(N-(5-(6-cyano-5-(((S)-1-(((S)-1-cyanoethyl)(methyl...)
Affinity DataIC50:  12.6nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397681((S)-N-(5-(6-cyano-5-((1-((cyanomethyl)(methyl)amin...)
Affinity DataIC50:  12.6nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397781((S)-N-(5-(6-cyano-5-((1-((2,2-difluoroethyl)(methy...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397660(N-(5-(4-cyano-3-((1-((2-hydroxyethyl)(methyl)amino...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397703(N-(5-(6-cyano-5-((2-((2,2-difluoroethyl)(2-hydroxy...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397672(N-(5-(6-cyano-5-((1-(methyl(2,2,2-trifluoroethyl)a...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397713(N-(5-(6-cyano-5-((2-((2,2-difluoroethyl)(2-methoxy...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397727((S)-N-(5-(6-cyano-5-((2-oxo-2-(2-(trifluoromethyl)...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397738((1R,2R)-N-(5-(6-cyano-5-(((S)-1-(dimethylamino)-1-...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397712(N-(5-(6-cyano-5-(((S)-1-((S)-3-cyanomorpholino)-1-...)
Affinity DataIC50:  15.8nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397760((S)-N-(5-(6-cyano-5-((1-(dimethylamino)-1-oxopropa...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397770(N-(5-(6-cyano-5-(((S)-1-((S)-3-fluoropyrrolidin-1-...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397650((S)-N-(5-(4-cyano-3-((1-((2-hydroxyethyl)(methyl)a...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397654((S)-N-(5-(4-cyano-3-((1-(dimethylamino)-1-oxobutan...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397678(N-(5-(6-cyano-5-((1-((2-fluoroethyl)(methyl)amino)...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397687((S)-N-(5-(6-cyano-5-((1-((2-fluoroethyl)(methyl)am...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397700(N-(5-(6-cyano-5-(((2S)-1-((1-cyanoethyl)(methyl)am...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397722(N-(5-(6-cyano-5-(((S)-1-((S)-3-methylmorpholino)-1...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397739((1R,2S)-N-(5-(6-cyano-5-(((S)-1-(dimethylamino)-1-...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397743((S)-N-(5-(6-cyano-5-((1-(ethyl(methyl)amino)-1-oxo...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397745((S)-N-(5-(6-cyano-5-((1-((2,2-difluoroethyl)amino)...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397674(N-(5-(6-cyano-5-((1-((cyanomethyl)(methyl)amino)-1...)
Affinity DataIC50:  20nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Takeda California

Curated by ChEMBL
LigandPNGBDBM50234302(CHEMBL4086393)
Affinity DataIC50:  25nMAssay Description:Inhibition of Axl (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397757(N-(5-(4-cyano-3-((2-(methyl(2,2,2-trifluoroethyl)a...)
Affinity DataIC50:  25.1nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
TargetSerine/threonine-protein kinase TBK1(Homo sapiens (Human))
Takeda Pharmaceutical

US Patent
LigandPNGBDBM397760((S)-N-(5-(6-cyano-5-((1-(dimethylamino)-1-oxopropa...)
Affinity DataIC50:  25.1nMAssay Description:TBK1 inhibition is determined using a 384 well μlate format in buffer containing 20 mM Hepes, pH 7.4, 10 mM MgCl2, 1 mM EDTA, 0.01% Brij-L23, 1 ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
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