Report error Found 51 Enz. Inhib. hit(s) with all data for entry = 50040113
Affinity DataIC50: 2nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 8nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 12nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 15nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 28nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 30nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 40nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 43nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 48nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 50nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 58nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 66nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 70nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 110nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 150nMAssay Description:Inhibition of KHKC in human HepG2 cells assessed as level of fructose-1-phosphateMore data for this Ligand-Target Pair
Affinity DataIC50: 300nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 440nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: <500nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 800nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of recombinant human hepatic KHKCMore data for this Ligand-Target Pair
TargetCasein kinase I isoform delta(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of CSNK1D by FRET assayMore data for this Ligand-Target Pair
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of INSR by FRET assayMore data for this Ligand-Target Pair
TargetGlycogen synthase kinase-3 beta(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of GSK3B by FRET assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Nek2(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of NEK2 by FRET assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk2(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of CHEK2 by FRET assayMore data for this Ligand-Target Pair
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of AURKA by FRET assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase 26(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of MST4 by FRET assayMore data for this Ligand-Target Pair
TargetProtein kinase C theta type(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of PRKCQ by FRET assayMore data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of EGFR by FRET assayMore data for this Ligand-Target Pair
TargetEphrin type-B receptor 1(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of EPHB1 by FRET assayMore data for this Ligand-Target Pair
TargetInterleukin-1 receptor-associated kinase 4(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of IRAK4 by FRET assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk1(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of CHEK1 by FRET assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase pim-2(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of PIM2 by FRET assayMore data for this Ligand-Target Pair
TargetcAMP-dependent protein kinase catalytic subunit alpha(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of PRKACA by FRET assayMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of CDK1/cyclin B by FRET assayMore data for this Ligand-Target Pair
TargetDeath-associated protein kinase 3(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of DAPK3 by FRET assayMore data for this Ligand-Target Pair
Target5'-AMP-activated protein kinase catalytic subunit alpha-1/subunit beta-1/subunit gamma-1(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of AMPK A1/B1/G1 by FRET assayMore data for this Ligand-Target Pair
TargetRho-associated protein kinase 1(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of ROCK1 by FRET assayMore data for this Ligand-Target Pair
TargetActivin receptor type-1B(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of ALK4 by FRET assayMore data for this Ligand-Target Pair
TargetCalcium/calmodulin-dependent protein kinase type 1D(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of CAMK1D by FRET assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase PAK 3(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of PAK3 by FRET assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase PLK3(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of PLK3 by FRET assayMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 13(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of MAPK13 by FRET assayMore data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of AKT1 by FRET assayMore data for this Ligand-Target Pair
TargetRibosomal protein S6 kinase alpha-3(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of RPS6KA3 by FRET assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase JAK2(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of JAK2 by FRET assayMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase ABL1(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of ABL1 by FRET assayMore data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of NTRK1 by FRET assayMore data for this Ligand-Target Pair
TargetProto-oncogene tyrosine-protein kinase Src(Human)
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Janssen Pharmaceutical Companies of Johnson & Johnson
Curated by ChEMBL
Affinity DataIC50: <1.00E+4nMAssay Description:Inhibition of SRC by FRET assayMore data for this Ligand-Target Pair