Compile Data Set for Download or QSAR
Found 34 with Last Name = 'sannia' and Initial = 'l'
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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