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Found 119 Enz. Inhib. hit(s) with Target = 'AMP deaminase'
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 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
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
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
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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087295(2-(2-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...)
Affinity DataKi:  300nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(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:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087328(2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...)
Affinity DataKi:  790nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087304(2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...)
Affinity DataKi:  800nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087304(2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...)
Affinity DataKi:  800nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087331(6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...)
Affinity DataKi:  860nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087291(6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...)
Affinity DataKi:  920nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087321(2-[4-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]...)
Affinity DataKi:  970nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087296(2-(4-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...)
Affinity DataKi:  1.10E+3nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087290(2-(3-Chloro-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-im...)
Affinity DataKi:  1.40E+3nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAMP deaminase 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087310(2-(4-Chloro-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-im...)
Affinity DataKi:  1.70E+3nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087298(6-(8-Hydroxy-7,8-dihydro-6H-imidazo[4,5-d][1,3]dia...)
Affinity DataKi:  2.10E+3nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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
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
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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087329(2-(3-Bromo-phenyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...)
Affinity DataKi:  2.40E+3nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More 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 2(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50087324(2-(3-Bromo-benzyl)-6-(8-hydroxy-7,8-dihydro-6H-imi...)
Affinity DataKi:  3.00E+3nMAssay Description:Evaluated for the inhibition of porcine heart or human L-type Adenosine 5'-monophosphate deaminase (AMPDA)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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