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)
University of Lyon

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133435BDBM50133435(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 Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50056221BDBM50056221(CHEMBL3322297)
Affinity DataKi:  1.60nMAssay Description:Inhibition of glycogen phosphorylase b (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/31/2016
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135554BDBM50135554(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133440BDBM50133440(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
University of Lyon

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50497973BDBM50497973(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 Depth
Date in BDB:
9/3/2020
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133443BDBM50133443(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135558BDBM50135558(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133442BDBM50133442(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133429BDBM50133429(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50149297BDBM50149297((S)-1-Ethyl-6-methyl-4-phenyl-1,4-dihydro-pyridine...)
Affinity DataKi:  11nMAssay Description:Inhibitory activity against rabbit muscle glycogen phosphorylase a in the absence of AMPMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/30/2012
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133438BDBM50133438(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135565BDBM50135565(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135553BDBM50135553(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133444BDBM50133444(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136445BDBM50136445(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133433BDBM50133433(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
University of Lyon

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50382964BDBM50382964(CHEMBL2030481)
Affinity DataIC50: 24nMAssay Description:Binding affinity to rabbit muscular GPb by NMR binding assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/7/2013
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135562BDBM50135562(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133430BDBM50133430(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133431BDBM50133431(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135557BDBM50135557(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
University of Lyon

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148913BDBM50148913(CHEMBL3770455)
Affinity DataKi:  31nMAssay Description:Competitive inhibition of rabbit muscle glycogen phosphorylase-b using alpha-D-glucose-1-phosphate as substrate by Dixon plot analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/23/2017
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136451BDBM50136451(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133441BDBM50133441(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136437BDBM50136437(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136447BDBM50136447(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133432BDBM50133432(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
University of Lyon

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50497969BDBM50497969(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 Depth
Date in BDB:
9/3/2020
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133447BDBM50133447(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136424BDBM50136424(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136435BDBM50136435(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136418BDBM50136418(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136428BDBM50136428(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135560BDBM50135560(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136448BDBM50136448(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135550BDBM50135550(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Rabbit)
University of Lyon

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148913BDBM50148913(CHEMBL3770455)
Affinity DataKi:  65nMAssay Description:Competitive inhibition of rabbit muscle glycogen phosphorylase-a assessed as release of inorganic phosphate using varying levels of glucose-1-phospha...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/27/2018
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136416BDBM50136416(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136440BDBM50136440(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135567BDBM50135567(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136430BDBM50136430(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136450BDBM50136450(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136414BDBM50136414(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50133434BDBM50133434(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136443BDBM50136443(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50136444BDBM50136444(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135559BDBM50135559(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50135561BDBM50135561(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172969BDBM50172969(4-(4-Methyl-3-oxo-3,4-dihydro-quinoxalin-2-ylamino...)
Affinity DataIC50: 110nMAssay Description:Inhibitory concentration against glycogen phosphorylase of rabbit muscleMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2012
Entry Details Article
PubMed
TargetGlycogen phosphorylase, muscle form(Human)
University of Thessaly

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172978BDBM50172978(N-Isoxazol-3-yl-4-(4-methyl-3-oxo-3,4-dihydro-quin...)
Affinity DataIC50: 110nMAssay Description:Inhibitory concentration against glycogen phosphorylase of rabbit muscleMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/4/2012
Entry Details Article
PubMed
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