Compile Data Set for Download or QSAR

Found 158 hits of Enzyme Inhibition Constant Data   

TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245691(9-hydroxy-6-(3-(methylamino)propyl)-4-phenylpyrrol...)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245342(4-(2-Chlorophenyl)-9-hydroxy-6-[2-hydroxy-3-(methy...)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245693(4-(2,6-dichlorophenyl)-9-hydroxy-6-(3-(methylamino...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245523(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245496(4-(2,6-Dichlorophenyl)-9-hydroxy-6-(3-hydroxypropy...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245387(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 7nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245457(4-(2,6-Dichlorophenyl)-9-hydroxy-6-(2-hydroxyethyl...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50232241(4-(2-Chlorophenyl)-9-hydroxy-6-(3-hydroxypropyl)-p...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245425(4-(2-Chlorophenyl)-9-hydroxy-6-[2-(1H-1,2,4-triazo...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245384(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192371(4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazol...)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245692(4-(2-chlorophenyl)-9-hydroxy-6-(3-(methylamino)pro...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245386(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245458(4-(4-(2-Chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245341(3-(4-(2,6-dichlorophenyl)-9-hydroxy-1,3-dioxo-2,3-...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245525(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245459(4-(2-Chlorophenyl)-9-hydroxy-6-[3-(1H-tetrazol-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245497(9-Hydroxy-6-(3-hydroxypropyl)-4-(2-methoxyphenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245426(4-(2-Chlorophenyl)-9-hydroxy-6-[2-(1H-1,2,4-triazo...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245522(3-(9-Hydroxy-1,3-dioxo-4-phenyl-2,3-dihydropyrrolo...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245731(6-[3-(Dimethylamino)propyl]-9-hydroxy-4-phenylpyrr...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245423(4-(2-Chlorophenyl)-9-hydroxy-6-[2-(1H-tetrazol-5-y...)copy SMILEScopy InChI
Affinity DataIC50: 21nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245549(4-(2-Chlorophenyl)-6-(2,3-dihydroxypropyl)-9-hydro...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245344(3-(9-hydroxy-1,3-dioxo-4-phenyl-2,3-dihydropyrrolo...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245424(4-(2-Chlorophenyl)-9-hydroxy-6-[2-(4H-1,2,4-triazo...)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245455(9-Hydroxy-6-(2-hydroxyethyl)-4-phenylpyrrolo[3,4-c...)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245548(4-(2-Chlorophenyl)-9-hydroxy-6-(3-methoxypropyl)-p...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245303(CHEMBL518048 | N-[2-(Dimethylamino)ethyl]-3-(9-hyd...)copy SMILEScopy InChI
Affinity DataIC50: 27nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192399(4-(2,6-dichlorophenyl)-9-hydroxypyrrolo[3,4-c]carb...)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245732(4-(2-chlorophenyl)-6-(3-(dimethylamino)propyl)-9-h...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245546(CHEMBL487891 | Methyl 3-(4-(2-chlorophenyl)-9-hydr...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245497(9-Hydroxy-6-(3-hydroxypropyl)-4-(2-methoxyphenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245343(4-(2-Chlorophenyl)-6-[3-(dimethylamino)-2-hydro-xy...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245547(4-(4-(2-Chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 33nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245522(3-(9-Hydroxy-1,3-dioxo-4-phenyl-2,3-dihydropyrrolo...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245304(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245146(6-(3-(1H-imidazol-1-yl)propyl)-9-hydroxy-4-phenylp...)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245456(4-(2-Chlorophenyl)-6-(2-hydroxyethyl)-9-hydroxypyr...)copy SMILEScopy InChI
Affinity DataIC50: 45nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192349(9-HYDROXY-4-PHENYLPYRROLO[3,4-C]CARBAZOLE-1,3(2H,6...)copy SMILEScopy InChI
Affinity DataIC50: 47nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245304(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 53nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245147(6-(3-(1H-imidazol-1-yl)propyl)-4-(2-chlorophenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245523(3-(4-(2-chlorophenyl)-9-hydroxy-1,3-dioxo-2,3-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245573(6-(2-(dimethylamino)ethyl)-9-hydroxy-4-phenylpyrro...)copy SMILEScopy InChI
Affinity DataIC50: 54nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245147(6-(3-(1H-imidazol-1-yl)propyl)-4-(2-chlorophenyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 55nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192433(9-hydroxy-6-methyl-4-phenylpyrrolo[3,4-c]carbazole...)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192411(4-(2-chlorophenyl)-9-hydroxy-6-methylpyrrolo[3,4-c...)copy SMILEScopy InChI
Affinity DataIC50: 57nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245342(4-(2-Chlorophenyl)-9-hydroxy-6-[2-hydroxy-3-(methy...)copy SMILEScopy InChI
Affinity DataIC50: 57nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245343(4-(2-Chlorophenyl)-6-[3-(dimethylamino)-2-hydro-xy...)copy SMILEScopy InChI
Affinity DataIC50: 58nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192400(6-butyl-4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]...)copy SMILEScopy InChI
Affinity DataIC50: 59nMAssay Description:Inhibition of human Wee1 assessed as polyornithine-tyrosine copolymer phosphorylationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50245495(9-Hydroxy-6-(3-hydroxypropyl)-4-phenylpyrrolo-[3,4...)copy SMILEScopy InChI
Affinity DataIC50: 59nMAssay Description:Inhibition of Chk1 kinase assessed as GST-Cdc25 phosphorylation by Western blot determinationMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36MCPubMed
Displayed 1 to 50 (of 158 total ) | Next | Last >>* indicates data uncertainty>20%