Compile Data Set for Download or QSAR
Report error Found 37 Enz. Inhib. hit(s) with all data for entry = 50029701
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287030BDBM50287030(2-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 34nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287034BDBM50287034(2-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 50nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287023BDBM50287023(N-tert-Butyl-2-(4-hydroxy-2-oxo-6-phenyl-2H-pyran-...)
Affinity DataIC50: 190nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287038BDBM50287038(3-Benzylsulfanyl-4-hydroxy-6-(4-hydroxy-3,5-dimeth...)
Affinity DataIC50: 250nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287021BDBM50287021(3-Benzylsulfanyl-6-(3,5-dimethyl-phenyl)-4-hydroxy...)
Affinity DataIC50: 260nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287026BDBM50287026(4-(5-Benzylsulfanyl-4-hydroxy-6-oxo-6H-pyran-2-yl)...)
Affinity DataIC50: 360nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287012BDBM50287012(3-Benzylsulfanyl-6-(2,3-dihydro-benzo[1,4]dioxin-6...)
Affinity DataIC50: 490nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287036BDBM50287036(3-Benzylsulfanyl-4-hydroxy-6-(3-trifluoromethyl-ph...)
Affinity DataIC50: 600nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287010BDBM50287010(2-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 619nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287025BDBM50287025(3-Benzylsulfanyl-6-(3,5-bis-trifluoromethyl-phenyl...)
Affinity DataIC50: 630nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287018BDBM50287018(3-Benzylsulfanyl-6-(3-chloro-phenyl)-4-hydroxy-pyr...)
Affinity DataIC50: 690nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287027BDBM50287027(3-Benzylsulfanyl-4-hydroxy-6-(4-hydroxy-phenyl)-py...)
Affinity DataIC50: 690nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287011BDBM50287011(3-Benzylsulfanyl-4-hydroxy-6-(4-methoxy-3-methyl-p...)
Affinity DataIC50: 740nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287041BDBM50287041(3-Benzylsulfanyl-6-(2,3-dihydro-benzo[1,4]dioxin-6...)
Affinity DataIC50: 790nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287022BDBM50287022(3-Benzylsulfanyl-4-hydroxy-6-m-tolyl-pyran-2-one |...)
Affinity DataIC50: 860nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287019BDBM50287019(3-Benzylsulfanyl-4-hydroxy-6-(3-methoxy-phenyl)-py...)
Affinity DataIC50: 990nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287031BDBM50287031(2-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287039BDBM50287039(3-Benzylsulfanyl-4-hydroxy-6-(3-hydroxy-phenyl)-py...)
Affinity DataIC50: 1.19E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287014BDBM50287014(2-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 1.20E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287016BDBM50287016(3-Benzylsulfanyl-4-hydroxy-6-(4-methoxy-phenyl)-py...)
Affinity DataIC50: 1.63E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 2568BDBM2568(3-(benzylsulfanyl)-4-hydroxy-6-phenyl-2H-pyran-2-o...)
Affinity DataIC50: 1.70E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287040BDBM50287040(3-Benzylsulfanyl-6-(3-ethyl-phenyl)-4-hydroxy-pyra...)
Affinity DataIC50: 2.04E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287009BDBM50287009(3-Benzylsulfanyl-4-hydroxy-6-(3-trifluoromethoxy-p...)
Affinity DataIC50: 2.14E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287033BDBM50287033(3-Benzylsulfanyl-6-(2-chloro-phenyl)-4-hydroxy-pyr...)
Affinity DataIC50: 2.54E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287008BDBM50287008(3-(2,3-Dihydro-benzo[1,4]dioxin-6-ylmethylsulfanyl...)
Affinity DataIC50: 3.42E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287013BDBM50287013(4-Hydroxy-3-(4-methyl-benzylsulfanyl)-6-phenyl-pyr...)
Affinity DataIC50: 4.58E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287015BDBM50287015(4-Hydroxy-3-(2-methyl-benzylsulfanyl)-6-phenyl-pyr...)
Affinity DataIC50: 5.37E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287017BDBM50287017(3-Benzylsulfanyl-4-hydroxy-6-(2-hydroxy-phenyl)-py...)
Affinity DataIC50: 6.00E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287024BDBM50287024(3-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 6.15E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287037BDBM50287037(4-Hydroxy-3-(3-methyl-benzylsulfanyl)-6-phenyl-pyr...)
Affinity DataIC50: 8.54E+3nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287043BDBM50287043(4-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 1.00E+4nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287020BDBM50287020(4-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 1.02E+4nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287029BDBM50287029(3-Benzylsulfanyl-4-hydroxy-6-p-tolyl-pyran-2-one |...)
Affinity DataIC50: 1.23E+4nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287042BDBM50287042(3-Benzylsulfanyl-4-hydroxy-6-o-tolyl-pyran-2-one |...)
Affinity DataIC50: 1.42E+4nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287035BDBM50287035(3-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 1.93E+4nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287028BDBM50287028(2-(4-Hydroxy-2-oxo-6-phenyl-2H-pyran-3-ylsulfanylm...)
Affinity DataIC50: 2.48E+4nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article

TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
TBA

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50287044BDBM50287044(4-(5-Benzylsulfanyl-4-hydroxy-6-oxo-6H-pyran-2-yl)...)
Affinity DataIC50: 1.00E+5nMAssay Description:In vitro inhibitory activity against HIV-1 protease(PR).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2010
Entry Details Article