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Found 151 with Last Name = 'oh' and Initial = 'dh'
TargetFatty acid-binding protein, adipocyte(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50310988(4-{[2-(methoxycarbonyl)-5-(2-thienyl)-3-thienyl]am...)
Affinity DataKi:  670nMAssay Description:Displacement of radiolabeled 1-anilinonapthalene 8-sulfonic acid from AFABP expressed in Escherichia coli BL21 (DE3) by fluorescence spectrophotometr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty acid-binding protein 5(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50310988(4-{[2-(methoxycarbonyl)-5-(2-thienyl)-3-thienyl]am...)
Affinity DataKi:  3.40E+3nMAssay Description:Displacement of radiolabeled 1-anilinonapthalene 8-sulfonic acid from EFABP expressed in Escherichia coli BL21 (DE3) by fluorescence spectrophotometr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty acid-binding protein, intestinal(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50310988(4-{[2-(methoxycarbonyl)-5-(2-thienyl)-3-thienyl]am...)
Affinity DataKi:  6.57E+3nMAssay Description:Displacement of radiolabeled 1-anilinonapthalene 8-sulfonic acid from IFABP expressed in Escherichia coli BL21 (DE3) by fluorescence spectrophotometr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty acid-binding protein, liver(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50310988(4-{[2-(methoxycarbonyl)-5-(2-thienyl)-3-thienyl]am...)
Affinity DataKi:  8.17E+3nMAssay Description:Displacement of radiolabeled 1-anilinonapthalene 8-sulfonic acid from LFABP expressed in Escherichia coli BL21 (DE3) by fluorescence spectrophotometr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty acid-binding protein, heart(Homo sapiens (Human))
University Of Minnesota

Curated by ChEMBL
LigandPNGBDBM50310988(4-{[2-(methoxycarbonyl)-5-(2-thienyl)-3-thienyl]am...)
Affinity DataKi:  9.07E+3nMAssay Description:Displacement of radiolabeled 1-anilinonapthalene 8-sulfonic acid from HFABP expressed in Escherichia coli BL21 (DE3) by fluorescence spectrophotometr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50609365(CHEMBL5282123)
Affinity DataIC50:  3.70nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609356(CHEMBL5278177)
Affinity DataIC50:  32nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609368(CHEMBL5287511)
Affinity DataIC50:  45nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609362(CHEMBL5282991)
Affinity DataIC50:  48nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609367(CHEMBL5279977)
Affinity DataIC50:  164nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609359(CHEMBL5280052)
Affinity DataIC50:  171nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609366(CHEMBL5287838)
Affinity DataIC50:  236nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609355(CHEMBL5276377)
Affinity DataIC50:  326nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609360(CHEMBL5272310)
Affinity DataIC50:  360nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609352(CHEMBL5290907)
Affinity DataIC50:  389nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609357(CHEMBL5285218)
Affinity DataIC50:  452nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609351(CHEMBL5275034)
Affinity DataIC50:  525nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609364(CHEMBL5286609)
Affinity DataIC50:  669nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609363(CHEMBL5289139)
Affinity DataIC50:  759nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609350(CHEMBL5278671)
Affinity DataIC50:  766nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609361(CHEMBL5279855)
Affinity DataIC50:  773nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM50609358(CHEMBL5274733)
Affinity DataIC50:  916nMAssay Description:Inhibition of ENPP1 (unknown origin)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
LigandPNGBDBM633382(4-(4-(aminomethyl)-phenyl)-7-methoxyphthalazin-1(2...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633379(4-(4-(aminomethyl)phenyl)-6-methoxyphthalazin-1(2H...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633384(4-(4-(aminomethyl)phenyl)-6,7-dimethoxy-2-methylph...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633385((R)-4-(4-(1-aminoethyl)phenyl)phthalazin-1(2H)-one...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633387(4-(4-(aminomethyl)-3-(trifluoromethyl)phenyl) phth...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633388(4-(1,2,3,4-tetrahydroisoquinolin-6-yl)phthalazin-1...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633417(N-(3-(4-oxo-3,4-dihydrophthalazin-1-yl)phenyl)sulf...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633418(N-(3-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)ph...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633419(N-(3-(3-benzyl-4-oxo-3,4-dihydrophthalazin-1-yl)ph...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633421(N-(4-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)ph...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633423(N-(3-(3-oxo-3,4-dihydrophthalazin-1-yl)benzyl)sulf...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633425(N-(3-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633426(N-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)benzyl) sul...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633427(N-(4-(3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633429(N-(4-(4-oxo-3-phenyl-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633432(N-(4-(7-methoxy-4-oxo-3,4-dihydrophthalazin-1-yl)b...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633433(N-(4-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633440(N-(4-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633450(7-(4-oxo-3,4-dihydrophthalazin-1-yl)-3,4-dihydrois...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633451(7-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1-yl)...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633452(N-(1-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)phenyl)e...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633453((R)-N-(1-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)phen...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633455(N-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)-2-(trifluo...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633456(N-methyl-N-(4-(4-oxo-3,4-dihydrophthalazin-1-yl)be...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633461(N-((1-(4-oxo-3,4-dihydrophthalazin-1-yl)piperidin-...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633462(N-((1-(6,7-dimethoxy-4-oxo-3,4-dihydrophthalazin-1...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633470(N-(4-((4-oxo-3,4-dihydrophthalazin-1-yl)methyl)phe...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
LigandPNGBDBM633471(N-(4-((3-methyl-4-oxo-3,4-dihydrophthalazin-1-yl)m...)
Affinity DataIC50: <1.00E+3nMAssay Description:ENPP1 hydrolyzes nucleotides or nucleotide derivatives to produce nucleoside -5′-monophosphate and pyrophosphate. in addition, ENPP1 hydrolyzes...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails US Patent
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