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Found 39 with Last Name = 'schauer-vukasinovic' and Initial = 'v'
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50251652(Biphenyl-4-carboxylic acid {[4-(adamantan-1-ylamin...)
Affinity DataKi:  9.43E+3nMAssay Description:Inhibition of 5-carboxyfluorescein-labeled Flu-Bak-BH3 peptide binding to Bcl-w by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50251651(Biphenyl-4-carboxylic acid methyl-[(3-nitro-4-pipe...)
Affinity DataKi:  1.08E+4nMAssay Description:Inhibition of 5-carboxyfluorescein-labeled Flu-Bak-BH3 peptide binding to Bcl-w by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50251616(CHEMBL521427 | biphenyl-4-carboxylic acid methyl-[...)
Affinity DataKi:  1.30E+4nMAssay Description:Inhibition of 5-carboxyfluorescein-labeled Flu-Bak-BH3 peptide binding to Bcl-w by fluorescence polarization assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147191(4-(1,5-Dimethyl-hex-4-enyl)-3-hydroxy-5-oxo-2-phen...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50404246(CHEMBL2111673)
Affinity DataIC50:  1.20E+3nMAssay Description:Evaluated for inhibition of Protease after after resynthesis and purificationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147191(4-(1,5-Dimethyl-hex-4-enyl)-3-hydroxy-5-oxo-2-phen...)
Affinity DataIC50:  1.30E+3nMAssay Description:Evaluated for inhibition of Protease after CLND/MS correction from the crude mixtureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147191(4-(1,5-Dimethyl-hex-4-enyl)-3-hydroxy-5-oxo-2-phen...)
Affinity DataIC50:  1.30E+3nMAssay Description:Evaluated for inhibition of Protease after after resynthesis and purificationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147193(3-Hydroxy-5-oxo-2-phenethyl-4-(1-phenyl-ethyl)-2,5...)
Affinity DataIC50:  2.00E+3nMAssay Description:Evaluated for inhibition of Protease after CLND/MS correction from the crude mixtureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147197(3-Hydroxy-5-oxo-2,4-diphenethyl-2,5-dihydro-furan-...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147193(3-Hydroxy-5-oxo-2-phenethyl-4-(1-phenyl-ethyl)-2,5...)
Affinity DataIC50:  4.00E+3nMAssay Description:Evaluated for inhibition of Protease after CLND/MS correction from the crude mixtureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147193(3-Hydroxy-5-oxo-2-phenethyl-4-(1-phenyl-ethyl)-2,5...)
Affinity DataIC50:  4.10E+3nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50404246(CHEMBL2111673)
Affinity DataIC50:  4.60E+3nMAssay Description:Evaluated for inhibition of Protease from the crude plate mixtureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50404246(CHEMBL2111673)
Affinity DataIC50:  4.60E+3nMAssay Description:Evaluated for inhibition of Protease after CLND/MS correction from the crude mixtureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50404246(CHEMBL2111673)
Affinity DataIC50:  5.00E+3nMAssay Description:Evaluated for inhibition of Protease after after resynthesis and purificationMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147193(3-Hydroxy-5-oxo-2-phenethyl-4-(1-phenyl-ethyl)-2,5...)
Affinity DataIC50:  6.00E+3nMAssay Description:Evaluated for inhibition of Protease from the crude plate mixtureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50181019(1-(2-methoxyphenethyl)-5-butyl-4-(2-phenoxyphenyl)...)
Affinity DataIC50:  8.09E+3nMAssay Description:Inhibition of Bclw by FP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147195(4-Benzyl-3-hydroxy-5-oxo-2-phenethyl-2,5-dihydro-f...)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50181020(1-(2-methoxybenzyl)-4-(2-phenoxyphenyl)-5-propyl-1...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibition of Bclw by FP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147191(4-(1,5-Dimethyl-hex-4-enyl)-3-hydroxy-5-oxo-2-phen...)
Affinity DataIC50:  1.50E+4nMAssay Description:Evaluated for inhibition of Protease from the crude plate mixtureMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147209(4-(4-tert-Butyl-phenyl)-3-hydroxy-5-oxo-2-phenethy...)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Pittsburgh

Curated by ChEMBL
LigandPNGBDBM50181021(1-biphenyl-3-ylmethyl-5-butyl-4-(2-methoxy-phenyl)...)
Affinity DataIC50:  2.69E+4nMAssay Description:Inhibition of Bclw by FP assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147201(4-Biphenyl-4-yl-3-hydroxy-5-oxo-2-phenethyl-2,5-di...)
Affinity DataIC50:  2.70E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147203(3-Hydroxy-2-isopropyl-5-oxo-4-(1-phenyl-ethyl)-2,5...)
Affinity DataIC50:  3.10E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147202((5-tert-Butylcarbamoyl-4-hydroxy-2-oxo-5-phenethyl...)
Affinity DataIC50:  4.70E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147200(3-Hydroxy-2-methyl-5-oxo-4-phenethyl-2,5-dihydro-f...)
Affinity DataIC50:  7.00E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50404246(CHEMBL2111673)
Affinity DataIC50:  8.40E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50404246(CHEMBL2111673)
Affinity DataIC50:  8.40E+4nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147190(3-Hydroxy-2-methyl-5-oxo-4-phenethyl-2,5-dihydro-f...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147198(3-Hydroxy-2-methyl-5-oxo-4-(1-phenyl-ethyl)-2,5-di...)
Affinity DataIC50:  1.05E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147204(3-Hydroxy-4-(1H-indol-3-yl)-5-oxo-2-phenethyl-2,5-...)
Affinity DataIC50:  1.07E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147194(4-(1,5-Dimethyl-hex-4-enyl)-3-hydroxy-2-methyl-5-o...)
Affinity DataIC50:  1.51E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147196(CHEMBL321798 | {4-Hydroxy-2-oxo-5-phenethyl-5-[(te...)
Affinity DataIC50:  1.93E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147208(3-Hydroxy-2-methyl-5-oxo-4-(1-phenyl-ethyl)-2,5-di...)
Affinity DataIC50:  2.24E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147199(3-Hydroxy-2-methyl-5-oxo-4-(1-phenyl-ethyl)-2,5-di...)
Affinity DataIC50:  2.44E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147206(3-Hydroxy-2-methyl-5-oxo-4-phenethyl-2,5-dihydro-f...)
Affinity DataIC50:  2.94E+5nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147207(3-Hydroxy-5-oxo-2-phenethyl-4-(3,4,5-trimethoxy-be...)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147192(3-Hydroxy-2-methyl-5-oxo-4-(3,4,5-trimethoxy-benzy...)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147205(3-Hydroxy-4-methylamino-5-oxo-2-phenethyl-2,5-dihy...)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Morphochem

Curated by ChEMBL
LigandPNGBDBM50147210(3-Hydroxy-2-methyl-5-oxo-4-(3,4,5-trimethoxy-benzy...)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibitory concentration against ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed