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Found 76 with Last Name = 'nathwani' and Initial = 'sm'
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM17292((1S,10R,11S,14S,15S)-15-methyltetracyclo[8.7.0.0^{...)
Affinity DataIC50:  5.60nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM17292((1S,10R,11S,14S,15S)-15-methyltetracyclo[8.7.0.0^{...)
Affinity DataIC50:  5.70nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031809(CHEMBL3360850)
Affinity DataIC50:  8nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031809(CHEMBL3360850)
Affinity DataIC50:  15nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031813(CHEMBL3360847)
Affinity DataIC50:  19nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031813(CHEMBL3360847)
Affinity DataIC50:  40nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM20607((2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethy...)
Affinity DataIC50:  61nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM20607((2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethy...)
Affinity DataIC50:  61nMAssay Description:Binding affinity to human ERalphaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031811(CHEMBL3360845)
Affinity DataIC50:  140nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031812(CHEMBL3360846)
Affinity DataIC50:  150nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM20607((2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethy...)
Affinity DataIC50:  188nMAssay Description:Binding affinity to human ERbetaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM20607((2-{4-[(1Z)-1,2-diphenylbut-1-en-1-yl]phenoxy}ethy...)
Affinity DataIC50:  190nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031810(CHEMBL3360843)
Affinity DataIC50:  230nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031810(CHEMBL3360843)
Affinity DataIC50:  980nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339514((+/-)-6-Ethyl-6-[4-[(2-chlorophenylthio)methyl]phe...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339521((+/-)-6-Ethyl-6-[4-[(4-fluorophenylthio)methyl]phe...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031812(CHEMBL3360846)
Affinity DataIC50:  1.10E+3nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031808(CHEMBL3360844)
Affinity DataIC50:  1.10E+3nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031811(CHEMBL3360845)
Affinity DataIC50:  1.20E+3nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339512((+/-)-6-Ethyl-6-[4-[(phenylthio)methyl]phenyl]-6,7...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339501((+/-)-6-Ethyl-6-[4-[(2-chloro-4-iodophenyloxy)meth...)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031808(CHEMBL3360844)
Affinity DataIC50:  1.40E+3nMAssay Description:Antagonist activity at human recombinant ERalpha by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031814(CHEMBL3360848)
Affinity DataIC50:  1.47E+3nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERalpha by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339510((+/-)-6-Ethyl-6-[4-[[4-[2-(trimethylsilyl)ethynyl]...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339522((+/-)-6-Ethyl-6-[4-[(4-bromophenylthio)methyl]phen...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339495((+/-)-6-Ethyl-6-[4-[(2-chloro-4-iodophenylthio)met...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339509((+/-)-6-Ethyl-6-[4-[(4-iodophenylthio)methyl]pheny...)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339518((+/-)-6-Ethyl-6-[4-[(3-trifluoromethylphenylthio)m...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339523((+/-)-6-Ethyl-6-[4-[(4-iodophenylthio)methyl]pheny...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339536((+/-)-6-Ethyl-6-[4-[(2-chloro-4-fluorophenylthio)m...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339529((+/-)-6-Ethyl-6-[4-[(2-methyl-6-chlorophenylthio)m...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339531((+/-)-6-Ethyl-6-[4-[(2,3-dichlorophenylthio)methyl...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339520((+/-)-6-Ethyl-6-[4-[(3-trifluoromethoxyphenylthio)...)
Affinity DataIC50:  3.20E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339498((+/-)-6-Ethyl-6-[4-[(2-imidazolylthio)methyl]pheny...)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339517((+/-)-6-Ethyl-6-[4-[(3-chlorophenylthio)methyl]phe...)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339505((+/-)-6-[4-[(Phenylthio)methyl]phenyl]-6,7-dihydro...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339516((+/-)-6-Ethyl-6-[4-[(3-fluorophenylthio)methyl]phe...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339506((+/-)-6-[4-[(2-Chlorophenylthio)methyl]phenyl]-6,7...)
Affinity DataIC50:  4.40E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339497((+/-)-6-Ethyl-6-[4-[(2-pyridylthio)methyl]phenyl]-...)
Affinity DataIC50:  4.50E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339513((+/-)-6-Ethyl-6-[4-[(2-fluorophenylthio)methyl]phe...)
Affinity DataIC50:  4.50E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetEstrogen receptor beta(Homo sapiens (Human))
Trinity College

Curated by ChEMBL
LigandPNGBDBM50031808(CHEMBL3360844)
Affinity DataIC50:  4.80E+3nMAssay Description:Displacement of fluorescein-labeled estrogen from human recombinant ERbeta by fluorescence polarization based competitive binding affinity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339508((+/-)-6-Ethyl-6-[4-[(2-chlorophenylthio)methyl]phe...)
Affinity DataIC50:  5.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339524((+/-)-6-Ethyl-6-[4-[(4-nitrophenylthio)methyl]phen...)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339525((+/-)-6-Ethyl-6-[4-[(4-trifluoromethoxyphenylthio)...)
Affinity DataIC50:  6.70E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339499((+/-)-6-Ethyl-6-[4-[(2-pyrazylthio)methyl]phenyl]-...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339500((+/-)-6-Ethyl-6-[4-[(2-pyrimidylthio)methyl]phenyl...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339502((+/-)-6-Ethyl-6-[4-[3-(2-hydroxy)ethylphenoxymethy...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339496((+/-)-6-Ethyl-6-[4-[(2,3,5,6-tetrafluorophenylthio...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339507((+/-)-6-[4-[(3-Trifluoromethylphenylthio)methyl]ph...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Universita` Di Siena

Curated by ChEMBL
LigandPNGBDBM50339534((+/-)-6-Ethyl-6-[4-[(3,4-dichlorophenylthio)methyl...)
Affinity DataIC50:  1.00E+4nMAssay Description:Inhibition of human adenosine kinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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