Compile Data Set for Download or QSAR
Found 88 with your filter
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158278(5-Chloro-1H-indole-2-carboxylic acid {[(1,1-dioxo-...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158249(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158255(5-Chloro-1H-indole-2-carboxylic acid {[cycloheptyl...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158254(5-Chloro-1H-indole-2-carboxylic acid [(cyanomethyl...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158283(5-Chloro-1H-indole-2-carboxylic acid {[cyclooctyl-...)copy SMILEScopy InChI
Affinity DataIC50: 32nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158308(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158303(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 49nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158295(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158304(5-Chloro-1H-indole-2-carboxylic acid [(cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158245(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158310(5-Chloro-1H-indole-2-carboxylic acid {[cyclononyl-...)copy SMILEScopy InChI
Affinity DataIC50: 82nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158315(5-Chloro-1H-indole-2-carboxylic acid [(butyl-cyclo...)copy SMILEScopy InChI
Affinity DataIC50: 82nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158261(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158264(5-Chloro-1H-indole-2-carboxylic acid [(allyl-cyclo...)copy SMILEScopy InChI
Affinity DataIC50: 96nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158274(5-Chloro-1H-indole-2-carboxylic acid {[cyclohexyl-...)copy SMILEScopy InChI
Affinity DataIC50: 99nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158276(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50065965(5-Chloro-1H-indole-2-carboxylic acid ((1S,2R)-1-be...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158288(5-Chloro-1H-indole-2-carboxylic acid {[butyl-(2-hy...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158272(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158248(5-Chloro-1H-indole-2-carboxylic acid {[cyclobutyl-...)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158247(5-Chloro-1H-indole-2-carboxylic acid {[(2-cyano-et...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158294(5-Chloro-1H-indole-2-carboxylic acid [(cyclohexyl-...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158301(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158290(5-Chloro-1H-indole-2-carboxylic acid [(butyl-methy...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158277(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158252(5-Chloro-1H-indole-2-carboxylic acid {[cyclopropyl...)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158296(5-Chloro-1H-indole-2-carboxylic acid [(cyclobutyl-...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158240(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158287(5-Chloro-1H-indole-2-carboxylic acid {[cyclopropyl...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158286(5-Chloro-1H-indole-2-carboxylic acid [(cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158307(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158262(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158237(5-Chloro-1H-indole-2-carboxylic acid [(methyl-phen...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158271(5-Chloro-1H-indole-2-carboxylic acid {[cyclodecyl-...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158320(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158246(5-Chloro-1H-indole-2-carboxylic acid ({cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158292(5-Chloro-1H-indole-2-carboxylic acid [(isobutyl-me...)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158273(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158298(5-Chloro-1H-indole-2-carboxylic acid {[(1-formyl-p...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158268(5-Chloro-1H-indole-2-carboxylic acid {[furan-2-ylm...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158260(({2-[(5-Chloro-1H-indole-2-carbonyl)-amino]-acetyl...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158279(5-Chloro-1H-indole-2-carboxylic acid {[tert-butyl-...)copy SMILEScopy InChI
Affinity DataIC50: 290nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158253(5-Chloro-1H-indole-2-carboxylic acid [(cycloheptyl...)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158241(5-Chloro-1H-indole-2-carboxylic acid {[benzyl-(2-h...)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158270(5-Chloro-1H-indole-2-carboxylic acid [(methyl-pyri...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158266(5-Chloro-1H-indole-2-carboxylic acid {[(2-hydroxy-...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158236(5-Chloro-1H-indole-2-carboxylic acid [(cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158306(5-Chloro-1H-indole-2-carboxylic acid [(methyl-pyri...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158243(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
TargetGlycogen phosphorylase, liver form(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50158242(5-Chloro-1H-indole-2-carboxylic acid {[cyclopentyl...)copy SMILEScopy InChI
Affinity DataIC50: 370nMAssay Description:Inhibitory concentration against glycogen phosphorylaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26W99K6PubMed
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