Compile Data Set for Download or QSAR
maximum 50k data
Report error Found 209 Enz. Inhib. hit(s) with all data for entry = 50018181
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192371(4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazol...)
Affinity DataIC50:  11nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192393(4-(2-chloro-3-hydroxyphenyl)-9-hydroxypyrrolo[3,4-...)
Affinity DataIC50:  12nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192422(4-(2-iodophenyl)-9-hydroxypyrrolo[3,4-c]carbazole-...)
Affinity DataIC50:  13nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192377(4-(2-chloro-6-methoxyphenyl)-9-hydroxypyrrolo[3,4-...)
Affinity DataIC50:  15nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192428(9-hydroxy-4-(3-thienyl)pyrrolo[3,4-c]carbazole-1,3...)
Affinity DataIC50:  17nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192382(4-(2,6-dichloro-3-hydroxyphenyl)-9-hydroxypyrrolo[...)
Affinity DataIC50:  18nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192402(4-(4-amino-2-methoxyphenyl)-9-hydroxypyrrolo[3,4-c...)
Affinity DataIC50:  19nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192435(4-(4-amino-2-bromophenyl)-9-hydroxypyrrolo[3,4-c]c...)
Affinity DataIC50:  20nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192389(4-(5-amino-2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]...)
Affinity DataIC50:  20nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192420(4-(4-aminophenyl)-9-hydroxypyrrolo[3,4-c]carbazole...)
Affinity DataIC50:  21nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192385(9-hydroxy-4-(4-hydroxyphenyl)pyrrolo[3,4-c]carbazo...)
Affinity DataIC50:  21nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192414(4-(3-amino-2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]...)
Affinity DataIC50:  21nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192381(4-(2-chloro-4-hydroxyphenyl)-9-hydroxypyrrolo[3,4-...)
Affinity DataIC50:  23nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192440(4-(2-bromophenyl)-9-hydroxypyrrolo[3,4-c]carbazole...)
Affinity DataIC50:  23nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192395(4-(4-amino-2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]...)
Affinity DataIC50:  24nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192374(9-hydroxy-4-(2-methoxyphenyl)pyrrolo[3,4-c]carbazo...)
Affinity DataIC50:  24nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192415(9-hydroxy-4-(1H-pyrrol-3-yl)pyrrolo[3,4-c]carbazol...)
Affinity DataIC50:  26nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192394(4-(2,6-dimethoxyphenyl)-9-hydroxypyrrolo[3,4-c]car...)
Affinity DataIC50:  27nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192399(4-(2,6-dichlorophenyl)-9-hydroxypyrrolo[3,4-c]carb...)
Affinity DataIC50:  28nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192437(4-(2,3-dichlorophenyl)-9-hydroxypyrrolo[3,4-c]carb...)
Affinity DataIC50:  28nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192344(4-(2-fluoro-6-methoxyphenyl)-9-hydroxypyrrolo[3,4-...)
Affinity DataIC50:  29nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192407(9-hydroxy-4-methyl-5-phenylpyrrolo[3,4-c]carbazole...)
Affinity DataIC50:  32nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192383(2-(9-hydroxy-1,3-dioxo-1,2,3,6-tetrahydropyrrolo[3...)
Affinity DataIC50:  32nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192363(9-hydroxy-4-(2-(methylthio)phenyl)pyrrolo[3,4-c]ca...)
Affinity DataIC50:  33nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192372(4-(2-chlorophenyl)-9-hydroxy-1H-[1]benzofuro[3,2-e...)
Affinity DataIC50:  33nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192427(4-(2,6-dibromophenyl)-9-hydroxypyrrolo[3,4-c]carba...)
Affinity DataIC50:  35nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192396(9-hydroxy-4-iodopyrrolo[3,4-c]carbazole-1,3(2H,6H)...)
Affinity DataIC50:  38nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192415(9-hydroxy-4-(1H-pyrrol-3-yl)pyrrolo[3,4-c]carbazol...)
Affinity DataIC50:  38nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192428(9-hydroxy-4-(3-thienyl)pyrrolo[3,4-c]carbazole-1,3...)
Affinity DataIC50:  42nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192423(4-(2-chloro-5-hydroxyphenyl)-9-hydroxypyrrolo[3,4-...)
Affinity DataIC50:  42nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192403(4-(2-chloro-6-hydroxyphenyl)-9-hydroxypyrrolo[3,4-...)
Affinity DataIC50:  45nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192443(9-hydroxy-4-(2-nitrophenyl)pyrrolo[3,4-c]carbazole...)
Affinity DataIC50:  47nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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...)
Affinity DataIC50:  47nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192424(4-(2,6-dichloro-4-hydroxyphenyl)-9-hydroxypyrrolo[...)
Affinity DataIC50:  49nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192367(4-(2-chlorophenyl)-6-ethyl-9-hydroxypyrrolo[3,4-c]...)
Affinity DataIC50:  50nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192387(4-(2-chlorophenyl)-9-hydroxy-6-isopropylpyrrolo[3,...)
Affinity DataIC50:  53nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192390(4-(3-chlorophenyl)-9-hydroxypyrrolo[3,4-c]carbazol...)
Affinity DataIC50:  55nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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...)
Affinity DataIC50:  56nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192411(4-(2-chlorophenyl)-9-hydroxy-6-methylpyrrolo[3,4-c...)
Affinity DataIC50:  57nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192400(6-butyl-4-(2-chlorophenyl)-9-hydroxypyrrolo[3,4-c]...)
Affinity DataIC50:  59nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192434(9-hydroxy-4-(2-hydroxyphenyl)pyrrolo[3,4-c]carbazo...)
Affinity DataIC50:  60nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192360(4-(2-chlorophenyl)-9-hydroxy-6-propylpyrrolo[3,4-c...)
Affinity DataIC50:  63nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192385(9-hydroxy-4-(4-hydroxyphenyl)pyrrolo[3,4-c]carbazo...)
Affinity DataIC50:  67nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192362(4-(3-aminophenyl)-9-hydroxypyrrolo[3,4-c]carbazole...)
Affinity DataIC50:  70nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192432(4-(3-fluorophenyl)-9-hydroxypyrrolo[3,4-c]carbazol...)
Affinity DataIC50:  73nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192369(3,9-dihydroxy-4-phenyl-2,3-dihydropyrrolo[3,4-c]ca...)
Affinity DataIC50:  74nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192379(4-(2,6-dimethylphenyl)-9-hydroxypyrrolo[3,4-c]carb...)
Affinity DataIC50:  75nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192356(4-(2-fluorophenyl)-9-hydroxypyrrolo[3,4-c]carbazol...)
Affinity DataIC50:  77nMAssay Description:Inhibition at human Chk1 in presence of 4 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192361(9-Hydroxy-4-phenyl-6-thia-2-aza-cyclopenta[c]fluor...)
Affinity DataIC50:  78nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetWee1-like protein kinase(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50192384(9-hydroxy-4-(3-hydroxyphenyl)pyrrolo[3,4-c]carbazo...)
Affinity DataIC50:  89nMAssay Description:Inhibition of human Wee1 in presence of 9.5 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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