Compile Data Set for Download or QSAR
Report error Found 27 Enz. Inhib. hit(s) with all data for entry = 50030626
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299323((S)-2-amino-4-hydroxy-N-(4-octylphenyl)butanamide ...)
Affinity DataIC50: 50nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299328((2S,3S)-3-hydroxy-N-(4-octylphenyl)pyrrolidine-2-c...)
Affinity DataIC50: 62nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299322((R)-2-amino-4-hydroxy-N-(4-octylphenyl)butanamide ...)
Affinity DataIC50: 180nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299331((2S,3S)-3-hydroxy-N-(4-octylbenzyl)pyrrolidine-2-c...)
Affinity DataIC50: 430nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50172238((2S,3R)-2-amino-3-hydroxy-N-(4-octylphenyl)butanam...)
Affinity DataIC50: 650nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299333((2R,3S)-2-((4-octylphenylamino)methyl)pyrrolidin-3...)
Affinity DataIC50: 740nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299318((2S,3S)-2-amino-3-hydroxy-N-(4-octylphenyl)butanam...)
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299317((2R,3R)-2-amino-3-hydroxy-N-(4-octylphenyl)butanam...)
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299316((2R,3S)-2-amino-3-hydroxy-N-(4-octylphenyl)butanam...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299314((+/-)-2-amino-3-hydroxy-3-methyl-N-(4-octylphenyl)...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299322((R)-2-amino-4-hydroxy-N-(4-octylphenyl)butanamide ...)
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299315((S)-3-hydroxy-2-(methylamino)-N-(4-octylphenyl)pro...)
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299319((2S,3S)-2-amino-3-hydroxy-N-(4-octylphenyl)pentana...)
Affinity DataIC50: 3.20E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299329((2S,3R)-3-hydroxy-N-(4-octylphenyl)pyrrolidine-2-c...)
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299326((+/-)-2-amino-4-hydroxy-N-(4-octylbenzyl)butanamid...)
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299325((S)-2-amino-6-hydroxy-N-(4-octylphenyl)hexanamide ...)
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299311((S)-2-amino-3-hydroxy-N-(4-octylphenyl)propanamide...)
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299321((R)-2-amino-3-(4-octylphenylamino)propan-1-ol | CH...)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299310((R)-2-amino-3-hydroxy-N-(4-octylphenyl)propanamide...)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50240721((E)-(2S,3R)-2-Dimethylamino-octadec-4-ene-1,3-diol...)
Affinity DataIC50: 5.70E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299332((2S,3S)-3-hydroxy-N-(4-octylphenethyl)pyrrolidine-...)
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299330((2S,3R,4R)-3,4-dihydroxy-N-(4-octylphenyl)pyrrolid...)
Affinity DataIC50: 8.30E+3nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299324((+/-)-2-amino-5-hydroxy-N-(4-octylphenyl)pentanami...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299327(3-amino-4-(4-octylphenylamino)butan-1-ol | CHEMBL5...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299320(2-amino-3-hydroxy-N-(4-octylbenzyl)propanamide | C...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299313((S)-2-amino-3-methoxy-N-(4-octylphenyl)propanamide...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed
TargetSphingosine kinase 1(Human)
Genzyme

Curated by ChEMBL
LigandPNGBDBM50299312((+/-)-2-amino-3-hydroxy-2-methyl-N-(4-octylphenyl)...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human sphingosine kinase 1 by off chip mobility shift assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/29/2010
Entry Details Article
PubMed