Compile Data Set for Download or QSAR
Found 28 Enz. Inhib. hit(s) with all data for assayid = 8 entry = 50006924
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055672(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055668(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055685(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055677(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM3152(2-{[2,6-dihydroxy-4-({[(3R,4R)-4-[(4-hydroxybenzen...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM3149(2-{[2,6-dihydroxy-4-({[(3R,4R)-3-[(4-hydroxybenzen...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055684(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM3153(2-{[2,6-dihydroxy-4-({[(1R,2R)-2-[(4-hydroxybenzen...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055676(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055666(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM3182(2-({2,6-dihydroxy-4-[({3-[(4-hydroxybenzene)amido]...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055681(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM3160(2-{[2,6-dihydroxy-4-({[(8R,9R)-9-[(4-hydroxybenzen...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055682(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM3150(2-{[2,6-dihydroxy-4-({[(1R,2R)-2-[(4-hydroxybenzen...)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055670(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055667(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055679(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055683(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 540nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055678(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 910nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055673(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055665(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055671(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055674(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM3151(2-{[2,6-dihydroxy-4-({[(3R,4R)-3-[(4-hydroxybenzen...)copy SMILEScopy InChI
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055669(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055680(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 9.60E+3nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed
TargetProtein kinase C alpha type(Homo sapiens (Human))
A Division of Eli Lilly & Company

Curated by ChEMBL
LigandPNGBDBM50055675(4-(2-Carboxy-6-hydroxy-benzoyl)-3,5-dihydroxy-benz...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibitory concentration against recombinant human Protein kinase C alpha isozymeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2J965HRPubMed