TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 0.400nMAssay Description:Inhibitory activity against HIV-1 Protease was determinedMore data for this Ligand-Target Pair
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 102nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 103nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 106nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 110nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 112nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 127nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 140nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 160nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 164nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 202nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 220nMAssay Description:Binding activity towards Human immunodeficiency virus-1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 220nMAssay Description:Inhibitory concentration against human immunodeficiency virus-1 protease; (Dimerization inhibitor)More data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 223nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 254nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 267nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 268nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 273nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 285nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 314nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 361nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 384nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 414nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
Affinity DataKi: 1.25E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
Affinity DataKi: 1.30E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.70E+3nMAssay Description:Inhibition of anthrax lethal factor by FRET assayMore data for this Ligand-Target Pair
Affinity DataKi: 2.20E+3nMAssay Description:Inhibition of Bacillus anthracis lethal factor by FRET assayMore data for this Ligand-Target Pair
Affinity DataKi: 2.30E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
TargetCapsid scaffolding protein(Human herpesvirus 1 (strain 17) (HHV-1) (Human her...)
Purdue University
Purdue University
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
Affinity DataKi: 3.00E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 3.00E+3nMAssay Description:Binding activity towards Human immunodeficiency virus-1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 3.00E+3nMAssay Description:Inhibition of anthrax lethal factor by FRET assayMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 3.00E+3nMAssay Description:Inhibitory concentration against human immunodeficiency virus -1 proteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 3.40E+3nMAssay Description:Binding affinity was evaluated for competitive inhibition of HIV-1 ProteaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Purdue University
Curated by ChEMBL
Purdue University
Curated by ChEMBL
Affinity DataKi: 4.90E+3nMAssay Description:Binding activity towards Human immunodeficiency virus-1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 6.00E+3nMAssay Description:Inhibition of anthrax lethal factor by FRET assayMore data for this Ligand-Target Pair
Affinity DataKi: 6.20E+3nMAssay Description:Inhibition of Bacillus anthracis lethal factor by FRET assayMore data for this Ligand-Target Pair
Affinity DataKi: 6.80E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Affinity DataKi: 8.30E+3nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.69E+4nMAssay Description:Inhibition of HIV1 protease by competitive inhibition assayMore data for this Ligand-Target Pair
Affinity DataKi: 4.01E+4nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair
Affinity DataKi: 8.80E+4nMAssay Description:Inhibition of HIV1 protease dimerization by Zhang-Poorman kinetic assayMore data for this Ligand-Target Pair