Compile Data Set for Download or QSAR
Report error Found 980 Enz. Inhib. hit(s) with Target = 'Glycogen phosphorylase, muscle form'
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM23210((1S,2R,4aS,6aS,6bR,8R,9R,10R,11R,12aR,12bR,14bS)-8...)
Affinity DatapH: 7.2 T: 2°CAssay Description:The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM23211((2S,3R,4S,5S,6R)-6-({[(2R,3R,4R,5S,6R)-3,4-dihydro...)
Affinity DatapH: 7.2 T: 2°CAssay Description:The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM23212((2S,3R,4S,5S,6R)-6-({[(2R,3R,4R,5S,6R)-3,4-dihydro...)
Affinity DatapH: 7.2 T: 2°CAssay Description:The activity of the compounds is determined by measuring the inhibitory effect of the compounds in the direction of glycogen synthesis, the conversio...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM35332(2-oxo-1,2-dihydropyridin-3-yl amide derivative, 7u)
Affinity DatapH: 7.2 T: 2°CAssay Description:RMGPa (Rabbit Muscle Glycogen Phosphorylase a) activity was measured in the direction of glycogen synthesis by the formation of inorganic phosphate f...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM50277972([5-(6-Amino-9-phenethyl-9H-purin-8-yl)-furan-2-yl]...)
Affinity DataEC50: >2.50E+5nMAssay Description:Inhibition of rabbit muscle glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM50277565({5-[6-Amino-9-(2,2-dimethyl-propyl)-9H-purin-8-yl]...)
Affinity DataEC50: >1.00E+5nMAssay Description:Inhibition of rabbit muscle glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM50133435(4-(2-Chloro-phenyl)-1-ethyl-6-methyl-1,4-dihydro-p...)
Affinity DataIC50: 1.60nMAssay Description:Binding affinity to rabbit muscular GPb by NMR binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135554(4-{3-[(4-Nitro-pyridine-2-carbonyl)-amino]-naphtha...)
Affinity DataIC50: 3nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133440(1-(4-Chloro-benzyl)-4-(2-chloro-phenyl)-6-methyl-1...)
Affinity DataIC50: 6nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM50497973(CHEMBL3323454)
Affinity DataIC50: 7nMAssay Description:Inhibition of rabbit muscle glycogen phosphorylase a assessed as inhibition of release of phosphate from glucose-1-phosphate after 30 mins by spectro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133443(4-(2-Chloro-phenyl)-1-ethyl-5-isobutylcarbamoyl-6-...)
Affinity DataIC50: 8.28nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135558(4-{3-Fluoro-2-[(4-nitro-pyridine-2-carbonyl)-amino...)
Affinity DataIC50: 9nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133442(4-(2-Chloro-phenyl)-6-methyl-1-(3-nitro-benzyl)-1,...)
Affinity DataIC50: 10nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133429(5-Benzylcarbamoyl-4-(2-chloro-phenyl)-1-ethyl-6-me...)
Affinity DataIC50: 10.6nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133438(4-(2-Chloro-phenyl)-1-(3,4-dimethoxy-benzyl)-6-met...)
Affinity DataIC50: 11nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135553(4-{3-[(4-Chloro-pyridine-2-carbonyl)-amino]-naphth...)
Affinity DataIC50: 12nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135565(4-{3-[(4-Methoxy-pyridine-2-carbonyl)-amino]-napht...)
Affinity DataIC50: 12nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133444(4-(2-Chloro-phenyl)-1-ethyl-5-isopropylcarbamoyl-6...)
Affinity DataIC50: 12.9nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136445(5-Chloro-1H-indole-2-carboxylic acid ((R)-2-oxo-1,...)
Affinity DataIC50: 14nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133433(4-(2-Chloro-phenyl)-1-ethyl-5-ethylcarbamoyl-6-met...)
Affinity DataIC50: 19.9nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM50382964(CHEMBL2030481)
Affinity DataIC50: 24nMAssay Description:Binding affinity to rabbit muscular GPb by NMR binding assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135562(4-{2-[(4-Nitro-pyridine-2-carbonyl)-amino]-phenoxy...)
Affinity DataIC50: 25nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133430(1-Benzyl-4-(2-chloro-phenyl)-6-methyl-1,4-dihydro-...)
Affinity DataIC50: 26nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135557(4-{3-[(4-Ethyl-pyridine-2-carbonyl)-amino]-naphtha...)
Affinity DataIC50: 29nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133431(1-(3-Chloro-benzyl)-4-(2-chloro-phenyl)-6-methyl-1...)
Affinity DataIC50: 29nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136451(5-Chloro-1H-indole-2-carboxylic acid (1-methyl-2-o...)
Affinity DataIC50: 32nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133441(4-(2-Chloro-phenyl)-1-(3,5-dichloro-benzyl)-6-meth...)
Affinity DataIC50: 37nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136437(5-chloro-N-(2-oxo-1,2,3,4-tetrahydroquinolin-3-yl)...)
Affinity DataIC50: 38nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136447(5-Chloro-1H-indole-2-carboxylic acid ((S)-2-oxo-1,...)
Affinity DataIC50: 39nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133432(4-(2-Chloro-phenyl)-1-(3,4-dichloro-benzyl)-6-meth...)
Affinity DataIC50: 41nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
China Pharmaceutical University

LigandPNGBDBM50497969(CHEMBL3323453)
Affinity DataIC50: 45nMAssay Description:Inhibition of rabbit muscle glycogen phosphorylase a assessed as inhibition of release of phosphate from glucose-1-phosphate after 30 mins by spectro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133447(4-(2-Chloro-phenyl)-6-methyl-1-(2,2,2-trifluoro-et...)
Affinity DataIC50: 52nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136424(5-Chloro-7-fluoro-1H-indole-2-carboxylic acid (1-m...)
Affinity DataIC50: 55nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136435(5-Chloro-1H-indole-2-carboxylic acid (2-oxo-2,3,4,...)
Affinity DataIC50: 55nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136418(1H-Indole-2-carboxylic acid (1-methyl-2-oxo-1,2,3,...)
Affinity DataIC50: 56nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135560(4-{3-[(4-Methyl-pyridine-2-carbonyl)-amino]-naphth...)
Affinity DataIC50: 57nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136428(5-Chloro-1H-indole-2-carboxylic acid ((S)-1-methyl...)
Affinity DataIC50: 57nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136448(5-Chloro-1H-indole-2-carboxylic acid ((R)-1-methyl...)
Affinity DataIC50: 58nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135550(4-{2-[(4-Chloro-pyridine-2-carbonyl)-amino]-3-fluo...)
Affinity DataIC50: 60nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136416(6-Chloro-1H-indole-2-carboxylic acid (1-methyl-2-o...)
Affinity DataIC50: 69nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136440(5-Bromo-1H-indole-2-carboxylic acid (1-methyl-2-ox...)
Affinity DataIC50: 73nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135567(4-{3-[(4-Trifluoromethyl-pyridine-2-carbonyl)-amin...)
Affinity DataIC50: 80nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136430(5-Chloro-1H-indole-2-carboxylic acid ((R)-2-oxo-2,...)
Affinity DataIC50: 83nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136450(7-Chloro-1H-indole-2-carboxylic acid (1-methyl-2-o...)
Affinity DataIC50: 88nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136414(5-Fluoro-1H-indole-2-carboxylic acid (1-methyl-2-o...)
Affinity DataIC50: 89nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50133434(4-(2-Chloro-phenyl)-1-(2,5-dichloro-benzyl)-6-meth...)
Affinity DataIC50: 91nMAssay Description:In vitro inhibitory activity against human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136443(5-Methyl-1H-indole-2-carboxylic acid (1-methyl-2-o...)
Affinity DataIC50: 98nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50136444(5-Chloro-1H-indole-2-carboxylic acid (1-methyl-2-o...)
Affinity DataIC50: 105nMAssay Description:Inhibitory concentration against recombinant human muscle glycogen phosphorylase a (HMGPa)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135559(4-{4-Fluoro-2-[(4-nitro-pyridine-2-carbonyl)-amino...)
Affinity DataIC50: 109nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50135561(4-{3-Fluoro-2-[(4-methoxy-pyridine-2-carbonyl)-ami...)
Affinity DataIC50: 110nMAssay Description:Inhibitory activity against HMGP(human muscle glycogen phosphorylase)More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
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