Compile Data Set for Download or QSAR
Found 49 with Last Name = 'derudas' and Initial = 'm'
TargetThymidylate kinase(Mycobacterium tuberculosis)
University of Gent

Curated by ChEMBL
LigandPNGBDBM50351772(CHEMBL1823506)copy SMILEScopy InChI
Affinity DataKi:  1.80E+4nMAssay Description:Inhibition of Mycobacterium tuberculosis Thymidylate kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q20R9PRRPubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM23399(4-{1-[(4-fluorophenyl)methyl]-1H-pyrrol-2-yl}-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 540nMAssay Description:Inhibition of HIV1 integrase strand transfer activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154420((Z)-4-(1-Benzyl-1H-indol-2-yl)-2-hydroxy-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154408((Z)-4-(1-Benzyl-1H-indol-3-yl)-2-hydroxy-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154411((Z)-4-(1-Ethyl-1H-indol-2-yl)-2-hydroxy-4-oxo-but-...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154406((Z)-2-Hydroxy-4-(5-methyl-5H-[1,3]dioxolo[4,5-f]in...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154419((Z)-4-(5-Benzyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154416((Z)-2-Hydroxy-4-(1-methyl-1H-indol-3-yl)-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetThymidine kinase(Human herpesvirus 3)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50481118(CHEMBL565370)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+3nMAssay Description:Displacement of [CH3-3H]deoxythymidine from Varicella zoster virus recombinant thymidine kinase after 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ06K1PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154414((Z)-4-(5-Ethyl-5H-[1,3]dioxolo[4,5-f]indol-7-yl)-2...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154410((Z)-4-(1-Ethyl-1H-indol-3-yl)-2-hydroxy-4-oxo-but-...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154417((Z)-2-Hydroxy-4-(5-methyl-5H-[1,3]dioxolo[4,5-f]in...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetThymidine kinase(Human herpesvirus 3)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50481116(Cf1743)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Displacement of [CH3-3H]deoxythymidine from Varicella zoster virus recombinant thymidine kinase after 30 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ06K1PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154413((Z)-4-(5-Ethyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154415((Z)-2-Hydroxy-4-(1-methyl-1H-indol-2-yl)-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154406((Z)-2-Hydroxy-4-(5-methyl-5H-[1,3]dioxolo[4,5-f]in...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154408((Z)-4-(1-Benzyl-1H-indol-3-yl)-2-hydroxy-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetThymidine kinase(Human herpesvirus 3)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50481117(CHEMBL585089)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Displacement of [CH3-3H]deoxythymidine from Varicella zoster virus recombinant thymidine kinase after 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ06K1PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154404(4-(5-Benzyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM23399(4-{1-[(4-fluorophenyl)methyl]-1H-pyrrol-2-yl}-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of HIV1 integrase 3' processing activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154411((Z)-4-(1-Ethyl-1H-indol-2-yl)-2-hydroxy-4-oxo-but-...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154420((Z)-4-(1-Benzyl-1H-indol-2-yl)-2-hydroxy-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154403(4-(1-Ethyl-1H-indol-3-yl)-2,4-dioxo-butyric acid m...)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154419((Z)-4-(5-Benzyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-...)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetThymidine kinase(Human herpesvirus 3)
Cardiff University

Curated by ChEMBL
LigandPNGBDBM50481115(CHEMBL565998)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+4nMAssay Description:Displacement of [CH3-3H]deoxythymidine from Varicella zoster virus recombinant thymidine kinase after 30 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2WQ06K1PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154418(4-(1-Methyl-1H-indol-2-yl)-2,4-dioxo-butyric acid ...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154414((Z)-4-(5-Ethyl-5H-[1,3]dioxolo[4,5-f]indol-7-yl)-2...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50190612((2Z)-4-[1-(4-fluoro-benzyl)-1H-pyrrol-2-yl]-2-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+4nMAssay Description:Inhibition of HIV1 integrase strand transfer activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154415((Z)-2-Hydroxy-4-(1-methyl-1H-indol-2-yl)-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154407(4-(5-Methyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154413((Z)-4-(5-Ethyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2...)copy SMILEScopy InChI
Affinity DataIC50: 5.50E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154409(4-(5-Methyl-5H-[1,3]dioxolo[4,5-f]indol-7-yl)-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154405(4-(5-Ethyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2,4-d...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated strand transfer reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50115579((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+4nMAssay Description:Inhibition of HIV1 integrase strand transfer activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50115579((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of HIV1 integrase strand transfer activity in presence of exogenous cobalt ionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50115579((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)copy SMILEScopy InChI
Affinity DataIC50: 8.20E+4nMAssay Description:Inhibition of HIV1 integrase 3' processing activity in presence of exogenous cobalt ionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154405(4-(5-Ethyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2,4-d...)copy SMILEScopy InChI
Affinity DataIC50: 8.50E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154410((Z)-4-(1-Ethyl-1H-indol-3-yl)-2-hydroxy-4-oxo-but-...)copy SMILEScopy InChI
Affinity DataIC50: 9.30E+4nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154404(4-(5-Benzyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154418(4-(1-Methyl-1H-indol-2-yl)-2,4-dioxo-butyric acid ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154417((Z)-2-Hydroxy-4-(5-methyl-5H-[1,3]dioxolo[4,5-f]in...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154407(4-(5-Methyl-5H-[1,3]dioxolo[4,5-f]indol-6-yl)-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154416((Z)-2-Hydroxy-4-(1-methyl-1H-indol-3-yl)-4-oxo-but...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154409(4-(5-Methyl-5H-[1,3]dioxolo[4,5-f]indol-7-yl)-2,4-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50154403(4-(1-Ethyl-1H-indol-3-yl)-2,4-dioxo-butyric acid m...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibitory concentration against HIV-1 integrase mediated 3' processing reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6R06PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50190612((2Z)-4-[1-(4-fluoro-benzyl)-1H-pyrrol-2-yl]-2-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.87E+5nMAssay Description:Inhibition of HIV1 integrase 3' processing activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50115579((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid | 2-...)copy SMILEScopy InChI
Affinity DataIC50: 3.33E+5nMAssay Description:Inhibition of HIV1 integrase 3' processing activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50125832((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid meth...)copy SMILEScopy InChI
Affinity DataIC50: 3.33E+5nMAssay Description:Inhibition of HIV1 integrase 3' processing activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed
TargetIntegrase(Human immunodeficiency virus 1)
Università di Sassari

Curated by ChEMBL
LigandPNGBDBM50125832((Z)-2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid meth...)copy SMILEScopy InChI
Affinity DataIC50: 3.33E+5nMAssay Description:Inhibition of HIV1 integrase strand transfer activityMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2T15384PubMed