Compile Data Set for Download or QSAR
Report error Found 27 Enz. Inhib. hit(s) with all data for entry = 50037595
TargetGlycogen phosphorylase, muscle form(Human)
Johnson & Johnson Pharmaceutical Research and Development

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)
Johnson & Johnson Pharmaceutical Research and Development

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
TargetGlycogen phosphorylase, muscle form(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172972BDBM50172972(N-Furan-2-ylmethyl-4-(4-methyl-3-oxo-3,4-dihydro-q...)
Affinity DataIC50: 120nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172983BDBM50172983(4-(7-Fluoro-4-methyl-3-oxo-3,4-dihydro-quinoxalin-...)
Affinity DataIC50: 140nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172977BDBM50172977(4-(4-Methyl-3-oxo-3,4-dihydro-quinoxalin-2-ylamino...)
Affinity DataIC50: 160nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172975BDBM50172975(4-(4-Ethyl-3-oxo-3,4-dihydro-quinoxalin-2-ylamino)...)
Affinity DataIC50: 190nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172961BDBM50172961(4-(4-Methyl-3-oxo-3,4-dihydro-pyrido[2,3-b]pyrazin...)
Affinity DataIC50: 190nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172971BDBM50172971(4-(4-Methyl-3-oxo-3,4-dihydro-quinoxalin-2-ylamino...)
Affinity DataIC50: 200nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172981BDBM50172981(4-(4,6-Dimethyl-3-oxo-3,4-dihydro-quinoxalin-2-yla...)
Affinity DataIC50: 280nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172984BDBM50172984(4-[4-(2-Hydroxy-ethyl)-3-oxo-3,4-dihydro-quinoxali...)
Affinity DataIC50: 320nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172970BDBM50172970(4-[4-(2-Morpholin-4-yl-ethyl)-3-oxo-3,4-dihydro-qu...)
Affinity DataIC50: 350nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172968BDBM50172968(4-[3-Oxo-4-(2-piperidin-1-yl-ethyl)-3,4-dihydro-qu...)
Affinity DataIC50: 420nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172962BDBM50172962(4-(4-Methyl-3-oxo-3,4-dihydro-quinoxalin-2-ylamino...)
Affinity DataIC50: 480nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172982BDBM50172982(4-[3-Oxo-4-(2-pyridin-1-yl-ethyl)-3,4-dihydro-quin...)
Affinity DataIC50: 580nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172966BDBM50172966(4-[4-(2-Dimethylamino-ethyl)-3-oxo-3,4-dihydro-qui...)
Affinity DataIC50: 710nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172974BDBM50172974(Isoxazole-5-carboxylic acid [4-(4-methyl-3-oxo-3,4...)
Affinity DataIC50: 710nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172963BDBM50172963(Isoxazole-3-carboxylic acid [4-(4-methyl-3-oxo-3,4...)
Affinity DataIC50: 730nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172973BDBM50172973(3-Phenylamino-1H-quinoxalin-2-one | CHEMBL371513)
Affinity DataIC50: 2.50E+3nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172985BDBM50172985(Furan-2-carboxylic acid [4-(4-methyl-3-oxo-3,4-dih...)
Affinity DataIC50: 2.50E+3nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172967BDBM50172967(1-Methyl-3-[4-(1H-pyrrol-2-yl)-phenylamino]-1H-qui...)
Affinity DataIC50: 2.50E+3nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172986BDBM50172986(3-(4-Furan-3-yl-phenylamino)-1-methyl-1H-quinoxali...)
Affinity DataIC50: 5.00E+3nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172980BDBM50172980((2-Oxo-3-{4-[(thiophen-2-ylmethyl)-carbamoyl]-phen...)
Affinity DataIC50: 5.70E+3nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172965BDBM50172965(4-(4-Methyl-3-oxo-3,4-dihydro-quinoxalin-2-ylamino...)
Affinity DataIC50: 1.00E+4nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172964BDBM50172964(Isoxazole-5-carboxylic acid [3-(4-methyl-3-oxo-3,4...)
Affinity DataIC50: 1.00E+4nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50370659BDBM50370659(CHEMBL1162917)
Affinity DataIC50: 1.00E+4nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172979BDBM50172979(1H-Pyrrole-2-carboxylic acid [4-(4-methyl-3-oxo-3,...)
Affinity DataIC50: 1.00E+4nMAssay 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)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50172976BDBM50172976(4-(4-Isopropyl-3-oxo-3,4-dihydro-quinoxalin-2-ylam...)
Affinity DataIC50: 1.00E+4nMAssay 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