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Found 208 with Last Name = 'chmielewski' and Initial = 'j'
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50069330((S)-2-((S)-2-{(2R,5S)-2-Benzyl-5-[(S)-2-((S)-2-ben...)
Affinity DataKi:  0.400nMAssay Description:Inhibitory activity against HIV-1 Protease was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59224(Pepstatin analog, 12)
Affinity DataKi:  96nM IC50:  360nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163700((S)-2-[(S)-2-(15-{(S)-1-[(R)-1-(1-Carbamoyl-2-hydr...)
Affinity DataKi:  102nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163699((S)-2-[(S)-2-(15-{(S)-1-[(R)-1-(1-Carbamoyl-2-hydr...)
Affinity DataKi:  103nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163688((S)-2-[(S)-2-(15-{(S)-1-[(R)-1-(1-Carbamoyl-2-hydr...)
Affinity DataKi:  106nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163711((S)-2-[(R)-2-(4-Benzyloxy-phenyl)-2-(15-{(S)-1-[(R...)
Affinity DataKi:  110nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370636(CHEMBL1791327)
Affinity DataKi:  112nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370640(CHEMBL1791339)
Affinity DataKi:  127nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370653(CHEMBL1791328)
Affinity DataKi:  140nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370638(CHEMBL1791330)
Affinity DataKi:  160nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370648(CHEMBL1791340)
Affinity DataKi:  164nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59223(Pepstatin analog, 11)
Affinity DataKi:  175nM IC50:  730nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370650(CHEMBL1791331)
Affinity DataKi:  202nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59213(Pepstatin analog, 1)
Affinity DataKi:  220nM IC50:  350nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370413(CHEMBL1791290)
Affinity DataKi:  220nMAssay Description:Binding activity towards Human immunodeficiency virus-1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370413(CHEMBL1791290)
Affinity DataKi:  220nMAssay Description:Inhibitory concentration against human immunodeficiency virus-1 protease; (Dimerization inhibitor)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163694((S)-3-(4-Benzoyl-phenyl)-2-((S)-3-carbamoyl-2-{15-...)
Affinity DataKi:  223nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163710(((S)-3-Carbamoyl-2-{15-[(S)-1-((R)-1-carbamoyl-2-p...)
Affinity DataKi:  254nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163717(2-((S)-3-Carbamoyl-2-{15-[(S)-1-((R)-1-carbamoyl-2...)
Affinity DataKi:  267nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163696((S)-2-((S)-3-Carbamoyl-2-{15-[(S)-1-((R)-1-carbamo...)
Affinity DataKi:  268nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370643(CHEMBL1791333)
Affinity DataKi:  273nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163707(2-((S)-3-Carbamoyl-2-{15-[(S)-1-((R)-1-carbamoyl-2...)
Affinity DataKi:  285nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370654(CHEMBL1791341)
Affinity DataKi:  314nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370645(CHEMBL1791342)
Affinity DataKi:  361nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163692((S)-2-((S)-3-Carbamoyl-2-{15-[(S)-1-((R)-1-carbamo...)
Affinity DataKi:  384nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370641(CHEMBL1791318)
Affinity DataKi:  414nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59220(Pepstatin analog, 8)
Affinity DataKi:  600nM IC50:  2.90E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59222(Pepstatin analog, 10)
Affinity DataKi:  650nM IC50:  2.50E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59219(Pepstatin analog, 7)
Affinity DataKi:  720nM IC50:  2.70E+3nMpH: 5.52Assay Description:A zhang-poorman assay confirms a competitive inhibition mechanism or inhibit HIV-1 PR as a dimerization or mixed type inhibitor.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59216(Pepstatin analog, 4)
Affinity DataKi:  1.13E+3nM IC50:  4.40E+3nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479598(CHEMBL478672)
Affinity DataKi:  1.25E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59217(Pepstatin analog, 5)
Affinity DataKi:  1.29E+3nM IC50:  4.90E+3nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479600(CHEMBL504512)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50215900(CHEMBL251733 | N-(3,4,5-trihydroxyphenethyl)oleami...)
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of anthrax lethal factor by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50375787(CHEMBL403034)
Affinity DataKi:  2.20E+3nMAssay Description:Inhibition of Bacillus anthracis lethal factor by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479594(CHEMBL510483)
Affinity DataKi:  2.30E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University

LigandPNGBDBM59214(Pepstatin analog, 2)
Affinity DataKi:  3.00E+3nM IC50:  5.90E+3nMpH: 5.52Assay Description:The competitive assay requires two inhibitors to act by a purely competitive mechanism, whereas the binding site of on the inhibitors has been establ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370412(CHEMBL449777)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50370412(CHEMBL449777)
Affinity DataKi:  3.00E+3nMAssay Description:Binding activity towards Human immunodeficiency virus-1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50215899(CHEMBL250711 | N-oleoyl-dopamine | Oleoyl dopamine...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of anthrax lethal factor by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50163697((S)-2-[(R)-3-Carbamoyl-3-(15-{(S)-1-[(S)-1-((S)-1-...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50069332((S)-2-[(S)-2-((S)-2-{(S)-2-[(S)-2-((S)-2-tert-Buto...)
Affinity DataKi:  3.40E+3nMAssay Description:Binding affinity was evaluated for competitive inhibition of HIV-1 ProteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50150552((E)-3-{(S)-1-[((S)-Carbamoyl-{11-[(S)-1-((S)-1-car...)
Affinity DataKi:  4.90E+3nMAssay Description:Binding activity towards Human immunodeficiency virus-1 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50215901(CHEMBL251734 | N-hydroxy-4-(2-oleamidoethyl)benzam...)
Affinity DataKi:  6.00E+3nMAssay Description:Inhibition of anthrax lethal factor by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLethal factor(Bacillus anthracis)
Purdue University

Curated by ChEMBL
LigandPNGBDBM50375786(CHEMBL271701)
Affinity DataKi:  6.20E+3nMAssay Description:Inhibition of Bacillus anthracis lethal factor by FRET assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479603(CHEMBL446001)
Affinity DataKi:  6.80E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479593(CHEMBL498854)
Affinity DataKi:  8.30E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479592(CHEMBL450301)
Affinity DataKi:  1.69E+4nMAssay Description:Inhibition of HIV1 protease by competitive inhibition assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479599(CHEMBL508493)
Affinity DataKi:  4.01E+4nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Purdue University

Curated by ChEMBL
LigandPNGBDBM50479596(CHEMBL454643)
Affinity DataKi:  8.80E+4nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
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