Compile Data Set for Download or QSAR
Found 266 with Last Name = 'huggins' and Initial = 'dj'
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM8125((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl N-[(2S...)copy SMILEScopy InChI
Affinity DataKi:  0.000200nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485746(CHEMBL2165886)copy SMILEScopy InChI
Affinity DataKi:  0.00100nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM8125((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl N-[(2S...)copy SMILEScopy InChI
Affinity DataKi:  0.00100nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM12877((5S)-3-(3-Acetylphenyl)-N-[(1S,2R)-1-benzyl-2-hydr...)copy SMILEScopy InChI
Affinity DataKi:  0.00100nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485764(CHEMBL2165912)copy SMILEScopy InChI
Affinity DataKi:  0.00300nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485740(CHEMBL2165903)copy SMILEScopy InChI
Affinity DataKi:  0.00300nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485744(CHEMBL2165917)copy SMILEScopy InChI
Affinity DataKi:  0.00300nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM8125((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl N-[(2S...)copy SMILEScopy InChI
Affinity DataKi:  0.00400nMAssay Description:Inhibition of HIV1 protease L10I, G48V, I54V, L63P and V82A mutant by FRET assayMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50180655(A-157378-0 | A-157378.0 | ABT-378 | CHEBI:31781 | ...)copy SMILEScopy InChI
Affinity DataKi:  0.00500nMAssay Description:Binding affinity to wild type HIV1 proteaseMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485760(CHEMBL2165901)copy SMILEScopy InChI
Affinity DataKi:  0.00500nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485747(CHEMBL2165900)copy SMILEScopy InChI
Affinity DataKi:  0.00500nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM577((3S)-oxolan-3-yl N-[(2S,3R)-4-[(4-aminobenzene)(2-...)copy SMILEScopy InChI
Affinity DataKi:  0.00700nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485769(CHEMBL2165881)copy SMILEScopy InChI
Affinity DataKi:  0.00800nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485753(CHEMBL2165891)copy SMILEScopy InChI
Affinity DataKi:  0.0170nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50368642(ACETYLPEPSTATIN)copy SMILEScopy InChI
Affinity DataKi:  0.0200nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2D79F84PubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485745(CHEMBL2165893)copy SMILEScopy InChI
Affinity DataKi:  0.0270nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM8125((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl N-[(2S...)copy SMILEScopy InChI
Affinity DataKi:  0.0270nMAssay Description:Inhibition of HIV1 protease L10I, L63P, A71V, G73S, I84V, L90M mutant by FRET assayMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485749(CHEMBL2165915)copy SMILEScopy InChI
Affinity DataKi:  0.0280nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM577((3S)-oxolan-3-yl N-[(2S,3R)-4-[(4-aminobenzene)(2-...)copy SMILEScopy InChI
Affinity DataKi:  0.0300nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM577((3S)-oxolan-3-yl N-[(2S,3R)-4-[(4-aminobenzene)(2-...)copy SMILEScopy InChI
Affinity DataKi:  0.0410nMAssay Description:Inhibition of HIV1 protease L10I, G48V, I54V, L63P and V82A mutant by FRET assayMore data for this Ligand-Target Pair
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485764(CHEMBL2165912)copy SMILEScopy InChI
Affinity DataKi:  0.0440nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485762(CHEMBL2165916)copy SMILEScopy InChI
Affinity DataKi:  0.0480nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485743(CHEMBL2165919)copy SMILEScopy InChI
Affinity DataKi:  0.0550nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485746(CHEMBL2165886)copy SMILEScopy InChI
Affinity DataKi:  0.0570nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485742(CHEMBL2165896)copy SMILEScopy InChI
Affinity DataKi:  0.0600nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM577((3S)-oxolan-3-yl N-[(2S,3R)-4-[(4-aminobenzene)(2-...)copy SMILEScopy InChI
Affinity DataKi:  0.195nMAssay Description:Inhibition of HIV1 protease L10I, L63P, A71V, G73S, I84V, L90M mutant by FRET assayMore data for this Ligand-Target Pair
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485773(CHEMBL2165890)copy SMILEScopy InChI
Affinity DataKi:  0.217nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485770(CHEMBL2165898)copy SMILEScopy InChI
Affinity DataKi:  0.230nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485740(CHEMBL2165903)copy SMILEScopy InChI
Affinity DataKi:  0.240nMAssay Description:Inhibition of HIV1 protease L10I, L63P, A71V, G73S, I84V, L90M mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485777(CHEMBL2165909)copy SMILEScopy InChI
Affinity DataKi:  0.243nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485742(CHEMBL2165896)copy SMILEScopy InChI
Affinity DataKi:  0.265nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485743(CHEMBL2165919)copy SMILEScopy InChI
Affinity DataKi:  0.284nMAssay Description:Inhibition of HIV1 protease L10I, G48V, I54V, L63P and V82A mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485749(CHEMBL2165915)copy SMILEScopy InChI
Affinity DataKi:  0.297nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485740(CHEMBL2165903)copy SMILEScopy InChI
Affinity DataKi:  0.299nMAssay Description:Inhibition of HIV1 protease L10I, G48V, I54V, L63P and V82A mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485749(CHEMBL2165915)copy SMILEScopy InChI
Affinity DataKi:  0.301nMAssay Description:Inhibition of HIV1 protease L10I, G48V, I54V, L63P and V82A mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485741(CHEMBL2165897)copy SMILEScopy InChI
Affinity DataKi:  0.303nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485747(CHEMBL2165900)copy SMILEScopy InChI
Affinity DataKi:  0.328nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485744(CHEMBL2165917)copy SMILEScopy InChI
Affinity DataKi:  0.333nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485749(CHEMBL2165915)copy SMILEScopy InChI
Affinity DataKi:  0.372nMAssay Description:Inhibition of HIV1 protease L10I, L63P, A71V, G73S, I84V, L90M mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485740(CHEMBL2165903)copy SMILEScopy InChI
Affinity DataKi:  0.377nMAssay Description:Inhibition of HIV1 protease I50V, A71V mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485771(CHEMBL2165880)copy SMILEScopy InChI
Affinity DataKi:  0.398nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485764(CHEMBL2165912)copy SMILEScopy InChI
Affinity DataKi:  0.400nMAssay Description:Inhibition of HIV1 protease L10I, G48V, I54V, L63P and V82A mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485751(CHEMBL2165908)copy SMILEScopy InChI
Affinity DataKi:  0.406nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485763(CHEMBL2165913)copy SMILEScopy InChI
Affinity DataKi:  0.426nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485743(CHEMBL2165919)copy SMILEScopy InChI
Affinity DataKi:  0.540nMAssay Description:Inhibition of HIV1 protease L10I, L63P, A71V, G73S, I84V, L90M mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485764(CHEMBL2165912)copy SMILEScopy InChI
Affinity DataKi:  0.563nMAssay Description:Inhibition of HIV1 protease L10I, L63P, A71V, G73S, I84V, L90M mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485748(CHEMBL2165894)copy SMILEScopy InChI
Affinity DataKi:  0.590nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetHIV-1 protease(Human immunodeficiency virus)
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485747(CHEMBL2165900)copy SMILEScopy InChI
Affinity DataKi:  0.599nMAssay Description:Inhibition of HIV1 protease L10I, G48V, I54V, L63P and V82A mutant by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50485775(CHEMBL2165883)copy SMILEScopy InChI
Affinity DataKi:  0.624nMAssay Description:Inhibition of wild type HIV1 protease by FRET assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8PKVPubMed
TargetProtease(Human immunodeficiency virus 1 (HIV-1))
Sanford-Burnham Medical Research Institute

Curated by ChEMBL
LigandPNGBDBM50213021(CHEBI:63621 | Fortovase | Invirase | Ro-31-8959 | ...)copy SMILEScopy InChI
Affinity DataKi:  0.650nMAssay Description:Binding affinity to wild type HIV1 proteaseMore data for this Ligand-Target Pair
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