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Found 23 with Last Name = 'rothfuss' and Initial = 'jm'
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50391056(CHEMBL2088421)
Affinity DataIC50:  0.280nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50099491(2-(4-(2-(3-cyclohexyl-1-(4-cyclohexylbutyl)ureido)...)
Affinity DataIC50:  0.460nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50391057(CHEMBL2088422)
Affinity DataIC50:  0.590nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor alpha(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50099489(2-(4-{2-[1-(4-Cyclohexyl-butyl)-3-(2-methoxy-pheny...)
Affinity DataIC50:  1.90nMAssay Description:Agonist activity at PPARalpha-LBD expressed in HEK293 cells co-expressing GAL4-DBD after 16 to 19 hrs by beta lactamase reporter gene assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50091801(6-Isobutyl-4-methyl-pyridin-2-ylamine | 6-isobutyl...)
Affinity DataIC50:  28nMAssay Description:Inhibition of human iNOSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267278(6-(3-Fluoropropyl)-4-methylpyridin-2-amine | CHEMB...)
Affinity DataIC50:  57.6nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50091801(6-Isobutyl-4-methyl-pyridin-2-ylamine | 6-isobutyl...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human nNOSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50091801(6-Isobutyl-4-methyl-pyridin-2-ylamine | 6-isobutyl...)
Affinity DataIC50:  150nMAssay Description:Inhibition of human eNOSMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267355(6-(4-Fluorobutyl)-4-methylpyridin-2-amine | CHEMBL...)
Affinity DataIC50:  170nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50091801(6-Isobutyl-4-methyl-pyridin-2-ylamine | 6-isobutyl...)
Affinity DataIC50:  193nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267272(6-(2-Fluoropropyl)-4-methylpyridin-2-amine | CHEMB...)
Affinity DataIC50:  220nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267274((E)-4-Methyl-6-(prop-1-enyl)pyridin-2-amine | CHEM...)
Affinity DataIC50:  282nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267272(6-(2-Fluoropropyl)-4-methylpyridin-2-amine | CHEMB...)
Affinity DataIC50:  490nMAssay Description:Inhibition of human recombinant nNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, brain(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267278(6-(3-Fluoropropyl)-4-methylpyridin-2-amine | CHEMB...)
Affinity DataIC50:  514nMAssay Description:Inhibition of human recombinant nNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267273(4-Methyl-6-(2-methylprop-1-enyl)pyridin-2-amine | ...)
Affinity DataIC50:  685nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267408(6-(4-Fluoro-2-methylbutyl)-4-methylpyridin-2-amine...)
Affinity DataIC50:  731nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267278(6-(3-Fluoropropyl)-4-methylpyridin-2-amine | CHEMB...)
Affinity DataIC50:  1.43E+3nMAssay Description:Inhibition of human recombinant eNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, endothelial(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267272(6-(2-Fluoropropyl)-4-methylpyridin-2-amine | CHEMB...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of human recombinant eNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267275(1-(6-Amino-4-methylpyridin-2-yl)propan-2-ol | CHEM...)
Affinity DataIC50:  1.78E+3nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267277(6-(2-(2-Fluoroethoxy)propyl)-4-methylpyridin-2-ami...)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267276(6-(2-Methoxypropyl)-4-methylpyridin-2-amine | CHEM...)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267409(6-(4-Methoxy-2-methylbutyl)-4-methylpyridin-2-amin...)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetNitric oxide synthase, inducible(Homo sapiens (Human))
Washington University

Curated by ChEMBL
LigandPNGBDBM50267410(4-Methyl-6-(2-methyl-4-(methylthio)butyl)pyridin-2...)
Affinity DataIC50: >5.00E+3nMAssay Description:Inhibition of human recombinant iNOS using 1 mM NADH and 2 uM L-arginine after 30 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed