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Found 105 with Last Name = 'thunnissen' and Initial = 'm'
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  4nMAssay Description:Inhibition of human cdc2/cyclin B assessed as [32P] incorporation in histone H1 from [gamma32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM7478(2-chloro-4-[(2-{[(1R)-1-(hydroxymethyl)-2-methylpr...)
Affinity DataIC50:  6nMAssay Description:Inhibition of human cdk5/p35More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM7478(2-chloro-4-[(2-{[(1R)-1-(hydroxymethyl)-2-methylpr...)
Affinity DataIC50:  6nMAssay Description:Inhibition of human cdk2/cyclin AMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM7478(2-chloro-4-[(2-{[(1R)-1-(hydroxymethyl)-2-methylpr...)
Affinity DataIC50:  6nMAssay Description:Inhibition of human cdc2/cyclin B assessed as [32P] incorporation in histone H1 from [gamma32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24285((3S)-3-amino-5-[(4-phenoxyphenyl)carbamoyl]pentano...)
Affinity DataIC50:  6nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM7478(2-chloro-4-[(2-{[(1R)-1-(hydroxymethyl)-2-methylpr...)
Affinity DataIC50:  9nMAssay Description:Inhibition of human cdk2/cyclin EMore data for this Ligand-Target Pair
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24282((2S)-2-amino-N-[4-(4-methylphenoxy)phenyl]pentaned...)
Affinity DataIC50:  13nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24291((4S)-4-amino-5-hydroxy-N-(4-phenoxyphenyl)pentanam...)
Affinity DataIC50:  14nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24287(3-[(2S)-2-amino-N-(4-phenoxyphenyl)pentanediamido]...)
Affinity DataIC50:  17nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24277((2S)-2-amino-4-{[4-(2-hydroxy-2-phenylethoxy)pheny...)
Affinity DataIC50:  17nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24276((2S)-2-amino-4-{[4-(2-oxo-2-phenylethoxy)phenyl]ca...)
Affinity DataIC50:  18nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24270((2S)-2-amino-4-[(4-phenoxyphenyl)carbamoyl]butanoi...)
Affinity DataIC50:  19nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24288(4-[(2S)-2-amino-N-(4-phenoxyphenyl)pentanediamido]...)
Affinity DataIC50:  19nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24256((2S)-2-amino-4-{[4-(benzyloxy)phenyl]carbamoyl}but...)
Affinity DataIC50:  20nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24289((2S)-2-amino-N-(2-hydroxyethyl)-N'-(4-phenoxypheny...)
Affinity DataIC50:  20nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24271((2S)-2-amino-N-(4-benzylphenyl)pentanediamide | Mo...)
Affinity DataIC50:  21nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24292((4S)-4,5-diamino-N-(4-phenoxyphenyl)pentanamide | ...)
Affinity DataIC50:  21nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24290((2S)-2-amino-N-(2-aminoethyl)-N'-(4-phenoxyphenyl)...)
Affinity DataIC50:  22nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24283((2S)-2-amino-4-({4-[4-(1H-pyrrol-1-yl)phenoxy]phen...)
Affinity DataIC50:  22nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24286(2-[(2S)-2-amino-N-(4-phenoxyphenyl)pentanediamido]...)
Affinity DataIC50:  22nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24261((2S)-2-amino-N-[4-(benzyloxy)phenyl]pentanediamide...)
Affinity DataIC50:  23nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24262((2S)-2-amino-N-[4-(benzyloxy)phenyl]-N'-hydroxypen...)
Affinity DataIC50:  25nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24284((2S)-2-amino-N-{4-[4-(furan-3-yl)phenoxy]phenyl}pe...)
Affinity DataIC50:  29nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24275((2S)-2-amino-4-{[4-(3-phenylpropoxy)phenyl]carbamo...)
Affinity DataIC50:  31nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  35nMAssay Description:Inhibition of human cdk2/cyclin EMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24259(Modified amino acid analog, 6a | methyl (2S)-2-ami...)
Affinity DataIC50:  39nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCdc2(Asterina pectinifera)
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  40nMAssay Description:Inhibition of starfish cdc2/cyclin B assessed as [32P] incorporation in histone H1 from 150 M [gamma32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24274((2S)-2-amino-4-{[4-(2-phenylethoxy)phenyl]carbamoy...)
Affinity DataIC50:  46nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCdc2(Asterina pectinifera)
University Of California

Curated by ChEMBL
LigandPNGBDBM7478(2-chloro-4-[(2-{[(1R)-1-(hydroxymethyl)-2-methylpr...)
Affinity DataIC50:  50nMAssay Description:Inhibition of starfish cdc2/cyclin B assessed as [32P] incorporation in histone H1 from 150 M [gamma32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24260(Modified amino acid analog, 6b | tert-butyl (2S)-2...)
Affinity DataIC50:  60nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24263(4-amino-N-[4-(benzyloxy)phenyl]butanamide | Modifi...)
Affinity DataIC50:  61nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  70nMAssay Description:Inhibition of human cdk2/cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  75nMAssay Description:Inhibition of human cdk5/p35More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Saccharomyces cerevisiae)
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  80nMAssay Description:Inhibition of Saccharomyces cerevisiae cdc28More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24298((4S)-4-amino-5-(1,3-dioxo-2,3-dihydro-1H-isoindol-...)
Affinity DataIC50:  85nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24294((2S)-2-amino-4-[(4-phenoxyphenyl)carbamoyl]butane-...)
Affinity DataIC50:  130nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoKEGGPC cidPC sid
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24281((2S)-2-amino-N-[4-(3-methylphenoxy)phenyl]pentaned...)
Affinity DataIC50:  150nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24244((2S)-2-amino-N-[4-(benzyloxy)phenyl]propanamide | ...)
Affinity DataIC50:  150nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24272((2S)-2-amino-4-{[4-(phenylamino)phenyl]carbamoyl}b...)
Affinity DataIC50:  210nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCdc2(Asterina pectinifera)
University Of California

Curated by ChEMBL
LigandPNGBDBM7478(2-chloro-4-[(2-{[(1R)-1-(hydroxymethyl)-2-methylpr...)
Affinity DataIC50:  250nMAssay Description:Inhibition of starfish cdc2/cyclin B assessed as [32P] incorporation in histone H1 from 1.5 mM [gamma32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24243(2-amino-N-[4-(benzyloxy)phenyl]acetamide | Amino a...)
Affinity DataIC50:  280nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50113707(2,6,9-Trisubstitute purine, 2 | 2-(2-hydroxyethyla...)
Affinity DataIC50:  340nMAssay Description:Inhibition of human cdc2/cyclin B assessed as [32P] incorporation in histone H1 from [gamma32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24296((4S)-4-amino-5-[(5-amino-1,3,4-thiadiazol-2-yl)sul...)
Affinity DataIC50:  350nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24297((4S)-4-amino-N-(4-phenoxyphenyl)-5-(1H-pyrrol-1-yl...)
Affinity DataIC50:  390nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCdc2(Asterina pectinifera)
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  500nMAssay Description:Inhibition of starfish cdc2/cyclin B assessed as [32P] incorporation in histone H1 from 1.5 mM [gamma32P]ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24251((4S)-4-amino-4-{[4-(benzyloxy)phenyl]carbamoyl}but...)
Affinity DataIC50:  680nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24268(Modified amino acid analog, 8c | methyl (2S)-2-ami...)
Affinity DataIC50:  730nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24295((4S)-4-amino-N-(4-phenoxyphenyl)-4-(4H-1,2,4-triaz...)
Affinity DataIC50:  740nMAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM27216((2R)-2-({6-[(3-chlorophenyl)amino]-9-(propan-2-yl)...)
Affinity DataIC50:  850nMAssay Description:Inhibition of human cdk4/cyclin D1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLeukotriene A-4 hydrolase(Homo sapiens (Human))
Berlex Biosciences

LigandPNGBDBM24255((2S)-2-amino-3-{[4-(benzyloxy)phenyl]carbamoyl}pro...)
Affinity DataIC50:  1.10E+3nMpH: 7.5 T: 2°CAssay Description:Compound potency against the peptidase activity of LTA4 hydrolase was measured by inhibition of the hydrolysis of L-alanine-p-nitroanilide to L-alani...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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