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Found 53 Enz. Inhib. hit(s) with Target = 'AMP deaminase 3'
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096172(1-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...)
Affinity DataKi:  2nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096172(1-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...)
Affinity DataKi:  2nMAssay Description:Inhibition of human recombinant AMPD3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096166(1-Benzyloxy-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo...)
Affinity DataKi:  9nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096165(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  15nMAssay Description:Inhibition of human recombinant AMPD3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096165(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  15nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096169(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  20nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087401(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  29nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096170(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  30nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096167(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  40nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087407(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  40nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087409(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  41nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096164(1,3-Dichloro-4-[2-(8-hydroxy-7,8-dihydro-6H-imidaz...)
Affinity DataKi:  50nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096171(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  90nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087411(2-Benzyl-2-[4-(8-hydroxy-7,8-dihydro-6H-imidazo[4,...)
Affinity DataKi:  170nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096175(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  220nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087408(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  250nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096162(1,3-Dichloro-4-[2-(8-hydroxy-7,8-dihydro-6H-imidaz...)
Affinity DataKi:  300nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096168(1-Benzyloxy-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo...)
Affinity DataKi:  300nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087414(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  360nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087405(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  360nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087332(2-Benzyl-6-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5-d...)
Affinity DataKi:  410nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087377(3-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  500nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096157(1,3-Dichloro-4-[2-(8-hydroxy-7,8-dihydro-6H-imidaz...)
Affinity DataKi:  500nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087404(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  900nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096177(6-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...)
Affinity DataKi:  960nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096174(1-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...)
Affinity DataKi:  1.00E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087402(6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087417(2-(4-Chloro-benzylcarbamoyl)-6-(8-hydroxy-7,8-dihy...)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096178(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  1.30E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096173(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  1.80E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087418(6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...)
Affinity DataKi:  2.10E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096163(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  2.30E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087410(2-Benzylcarbamoyl-6-(8-hydroxy-7,8-dihydro-6H-imid...)
Affinity DataKi:  2.40E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096176(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  2.40E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087413(2-Benzyl-2-[4-(8-hydroxy-7,8-dihydro-6H-imidazo[4,...)
Affinity DataKi:  2.60E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50003602((2R,3S,5R)-2-((R)-8-Hydroxy-7,8-dihydro-6H-imidazo...)
Affinity DataKi:  3.00E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096161(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  3.80E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087412(6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...)
Affinity DataKi:  4.20E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096159(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  5.00E+3nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087399(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  5.10E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087400(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  5.20E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087403(2-Cyclohexylcarbamoyl-6-(8-hydroxy-7,8-dihydro-6H-...)
Affinity DataKi:  5.20E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087406(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  6.00E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087415(2-Carbamoyl-6-(8-hydroxy-7,8-dihydro-6H-imidazo[4,...)
Affinity DataKi:  7.80E+3nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096158(6-Bromo-4-[2-(8-hydroxy-7,8-dihydro-6H-imidazo[4,5...)
Affinity DataKi:  1.40E+4nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50096160(4-[2-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  3.50E+4nMAssay Description:Inhibition of recombinant human E-type adenylate deaminaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087416(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  4.48E+4nMAssay Description:Inhibitory activity against porcine heart or recombinant human E-type AMPDAMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM154583(6-[4-({[(1S)-1-(isoquinolin-8-yl)ethyl]amino}methy...)
Affinity DataIC50:  75nMpH: 7.4Assay Description:AMPD1 was added to buffer A (50 mM HEPES, 150 mM KCl, 5 mM MgCl2, and 0.5 mMglutathione [pH 7.4]) to a concentration of 10 nM. A substrate mix consis...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Rattus norvegicus (Rat))
Astrazeneca R&D

LigandPNGBDBM154583(6-[4-({[(1S)-1-(isoquinolin-8-yl)ethyl]amino}methy...)
Affinity DataIC50:  400nMpH: 7.4Assay Description:AMPD1 was added to buffer A (50 mM HEPES, 150 mM KCl, 5 mM MgCl2, and 0.5 mMglutathione [pH 7.4]) to a concentration of 10 nM. A substrate mix consis...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 3(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50385586(CHEMBL2042530)
Affinity DataIC50:  900nMAssay Description:Inhibition of human recombinant AMPD3-1b expressed in Sf9 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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