Compile Data Set for Download or QSAR
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Report error Found 23 Enz. Inhib. hit(s) with all data for entry = 50005450
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492205(CHEMBL2397859)
Affinity DataIC50:  111nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492198(CHEMBL2397840)
Affinity DataIC50:  190nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492209(CHEMBL2397838)
Affinity DataIC50:  199nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492197(CHEMBL2397841)
Affinity DataIC50:  247nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492204(CHEMBL2397839)
Affinity DataIC50:  249nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492196(CHEMBL2397850)
Affinity DataIC50:  309nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492195(CHEMBL2397858)
Affinity DataIC50:  342nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492200(CHEMBL2397849)
Affinity DataIC50:  354nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492194(CHEMBL2397857)
Affinity DataIC50:  520nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492201(CHEMBL2397851)
Affinity DataIC50:  607nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492199(CHEMBL2397853)
Affinity DataIC50:  641nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492203(CHEMBL2397852)
Affinity DataIC50:  774nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492193(CHEMBL2397860)
Affinity DataIC50:  818nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492192(CHEMBL2397854)
Affinity DataIC50:  1.01E+3nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492202(CHEMBL2397847)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492191(CHEMBL2397855)
Affinity DataIC50:  1.36E+3nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492190(CHEMBL2397846)
Affinity DataIC50:  7.01E+3nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492207(CHEMBL2397845)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492208(CHEMBL2397856)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492206(CHEMBL2397844)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492189(CHEMBL2397842)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492187(CHEMBL2397848)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50492188(CHEMBL2397843)
Affinity DataIC50: >5.00E+4nMAssay Description:Inhibition of recombinant human GSK3 using YRRAAVPPSPSLSRHSSPHQ(pS)EDEEE as substrate preincubated for 10 mins followed by [33P-gamma]-ATP addition m...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed