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Found 122 Enz. Inhib. hit(s) with Target = 'Sorbitol dehydrogenase'
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118706((S)-1-(4-{2,6-Dimethyl-4-[2-(4-methyl-piperazin-1-...)
Affinity DataIC50:  4nMAssay Description:Concentration required for 50% for in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118710(1-(4-{4-[2-(2,4-Dimethyl-imidazol-1-yl)-pyrimidin-...)
Affinity DataIC50:  4nMAssay Description:Concentration required for 50% for in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118709(1-{4-[2,6-Dimethyl-4-(4-methyl-[1,3,5]triazin-2-yl...)
Affinity DataIC50:  5nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113497(1-(4-{(2S,6R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrimidin...)
Affinity DataIC50:  5nMAssay Description:Inhibition of recombinant rat sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113497(1-(4-{(2S,6R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrimidin...)
Affinity DataIC50:  6nMAssay Description:In vitro inhibition against human recombinant sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118706((S)-1-(4-{2,6-Dimethyl-4-[2-(4-methyl-piperazin-1-...)
Affinity DataIC50:  6nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118710(1-(4-{4-[2-(2,4-Dimethyl-imidazol-1-yl)-pyrimidin-...)
Affinity DataIC50:  7nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118708(1-{4-[2,6-Dimethyl-4-(4-phenyl-[1,3,5]triazin-2-yl...)
Affinity DataIC50:  7nMAssay Description:Concentration required for 50% for in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118709(1-{4-[2,6-Dimethyl-4-(4-methyl-[1,3,5]triazin-2-yl...)
Affinity DataIC50:  7nMAssay Description:Concentration required for 50% for in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113491(1-(4-{(3S,5R)-4-[2-(1-Hydroxy-ethyl)-pyrimidin-4-y...)
Affinity DataIC50:  8nMAssay Description:Inhibition of recombinant rat Sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108732(1-{4-[4-(3-Methyl-quinoxalin-2-yl)-piperazin-1-yl]...)
Affinity DataIC50:  8nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118711(1-{4-[4-(4,6-Dimethyl-[1,3,5]triazin-2-yl)-2,6-dim...)
Affinity DataIC50:  9nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118711(1-{4-[4-(4,6-Dimethyl-[1,3,5]triazin-2-yl)-2,6-dim...)
Affinity DataIC50:  9nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113494((R)-1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  10nMAssay Description:In vitro inhibition against human recombinant sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113496((S)-1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  10nMAssay Description:Concentration required for 50% in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108762(1-(4-{4-[2-(2-Hydroxy-ethyl)-pyrimidin-4-yl]-2,6-d...)
Affinity DataIC50:  10nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118708(1-{4-[2,6-Dimethyl-4-(4-phenyl-[1,3,5]triazin-2-yl...)
Affinity DataIC50:  10nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118712(1-(4-{2,6-Dimethyl-4-[2-(4-methyl-imidazol-1-yl)-p...)
Affinity DataIC50:  11nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113496((S)-1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  11nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108758(1-(4-{4-[2-(2-Hydroxy-ethyl)-pyrimidin-4-yl]-2-met...)
Affinity DataIC50:  12nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108754(1-[4-(4-Benzo[d]isothiazol-3-yl-piperazin-1-yl)-py...)
Affinity DataIC50:  12nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118712(1-(4-{2,6-Dimethyl-4-[2-(4-methyl-imidazol-1-yl)-p...)
Affinity DataIC50:  13nMAssay Description:Concentration required for 50% for in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118711(1-{4-[4-(4,6-Dimethyl-[1,3,5]triazin-2-yl)-2,6-dim...)
Affinity DataIC50:  16nMAssay Description:Concentration required for 50% for in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113494((R)-1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  17nMAssay Description:Inhibition of recombinant rat sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113493(1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrimidin...)
Affinity DataIC50:  18nMAssay Description:Inhibition of recombinant rat sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113498((R)-1-(4-{(3S,5R)-4-[2-((S)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  19nMAssay Description:In vitro inhibition against human recombinant Sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113493(1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrimidin...)
Affinity DataIC50:  19nMAssay Description:In vitro inhibition against human recombinant sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118713(1-{4-[4-(4-Hydroxymethyl-6-methyl-[1,3,5]triazin-2...)
Affinity DataIC50:  20nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108765(1-{4-[4-(4-Hydroxymethyl-6-methyl-pyrimidin-2-yl)-...)
Affinity DataIC50:  20nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108724(1-{4-[4-(4,6-Dimethyl-pyrimidin-2-yl)-piperazin-1-...)
Affinity DataIC50:  23nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108742(1-[4-(3-Methyl-4-oxazolo[5,4-c]pyridin-2-yl-pipera...)
Affinity DataIC50:  23nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108717(1-[4-(4-Oxazolo[5,4-c]pyridin-2-yl-piperazin-1-yl)...)
Affinity DataIC50:  24nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50102724(4-[2-(1-Hydroxy-ethyl)-pyrimidin-4-yl]-piperazine-...)
Affinity DataIC50:  27nMAssay Description:In vitro inhibitory activity against human SDHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113498((R)-1-(4-{(3S,5R)-4-[2-((S)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  27nMAssay Description:Inhibition of recombinant rat Sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113491(1-(4-{(3S,5R)-4-[2-(1-Hydroxy-ethyl)-pyrimidin-4-y...)
Affinity DataIC50:  28nMAssay Description:In vitro inhibition against human recombinant Sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113496((S)-1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  29nMAssay Description:Inhibition of recombinant rat sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108722(1-{4-[4-(2,6-Dimethyl-pyrimidin-4-yl)-piperazin-1-...)
Affinity DataIC50:  31nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108734(1-[4-(4-Oxazolo[5,4-b]pyridin-2-yl-piperazin-1-yl)...)
Affinity DataIC50:  32nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50409605(CHEMBL2111939)
Affinity DataIC50:  32nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50113496((S)-1-(4-{(3S,5R)-4-[2-((R)-1-Hydroxy-ethyl)-pyrim...)
Affinity DataIC50:  33nMAssay Description:In vitro inhibition against human recombinant sorbitol dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108741(1-[4-(4-Isoquinolin-1-yl-piperazin-1-yl)-pyrimidin...)
Affinity DataIC50:  34nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108750(1-[4-(4-Benzooxazol-2-yl-piperazin-1-yl)-pyrimidin...)
Affinity DataIC50:  35nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108759(1-[4-(4-Quinoxalin-2-yl-piperazin-1-yl)-pyrimidin-...)
Affinity DataIC50:  36nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108746(1-[4-(4-Benzo[d]isoxazol-3-yl-piperazin-1-yl)-pyri...)
Affinity DataIC50:  37nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Rattus norvegicus)
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118707(1-{4-[2,6-Dimethyl-4-(4-methyl-6-phenyl-[1,3,5]tri...)
Affinity DataIC50:  39nMAssay Description:Concentration required for 50% in vitro activity against rat SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108738(1-(4-{4-[2-(2-Hydroxy-ethyl)-pyrimidin-4-yl]-piper...)
Affinity DataIC50:  40nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50118707(1-{4-[2,6-Dimethyl-4-(4-methyl-6-phenyl-[1,3,5]tri...)
Affinity DataIC50:  43nMAssay Description:Concentration required for 50% for in vitro activity against human SDH (sorbitol dehydrogenase)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108760(1-[4-(4-Quinolin-2-yl-piperazin-1-yl)-pyrimidin-2-...)
Affinity DataIC50:  44nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108763(1-(4-{4-[2-(2-Hydroxy-ethyl)-pyrimidin-4-yl]-2-met...)
Affinity DataIC50:  59nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSorbitol dehydrogenase(Homo sapiens (Human))
Pfizer

Curated by ChEMBL
LigandPNGBDBM50108726(CHEMBL146805 | [4-(4-Benzo[d]isothiazol-3-yl-piper...)
Affinity DataIC50:  64nMAssay Description:Concentration required for 50% in vitro inhibition of recombinant human sorbitol dehydrogenase (h-SDH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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