null
SMILES C[C@@H]1C[C@H]2CN1CCn1[nH]c3c(cccc3c1=O)-c1nc3c(O2)cccc3[nH]c1=O
InChI Key InChIKey=KBLPHMRCKHFBJB-OLZOCXBDSA-N
PDB links: 1 PDB ID matches this monomer.
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 67 hits for monomerid = 50192071
TargetMitogen-activated protein kinase 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of MAPK1More data for this Ligand-Target Pair
TargetcAMP-dependent protein kinase catalytic subunit alpha/beta/gamma(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKAMore data for this Ligand-Target Pair
TargetProtein kinase C alpha type(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKCalphaMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of ERK2More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Chk1More data for this Ligand-Target Pair
TargetProtein kinase C eta type(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKCetaMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase D2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKD2More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
TargetMAP kinase-activated protein kinase 5(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PRAKMore data for this Ligand-Target Pair
TargetRibosomal protein S6 kinase alpha-3(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of RSK2More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
TargetMitogen-activated protein kinase 13(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of SAPK4More data for this Ligand-Target Pair
TargetProtein kinase C gamma type(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKCgammaMore data for this Ligand-Target Pair
Target3-phosphoinositide-dependent protein kinase 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PDK1More data for this Ligand-Target Pair
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PDGFRbetaMore data for this Ligand-Target Pair
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of c-RAFMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase PAK 2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PAK2More data for this Ligand-Target Pair
TargetCytoplasmic tyrosine-protein kinase BMX(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Bmx kinaseMore data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of FLT1More data for this Ligand-Target Pair
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of KDRMore data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of FGFR1More data for this Ligand-Target Pair
TargetProtein kinase C beta type(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKCbeta2More data for this Ligand-Target Pair
TargetMAP kinase-activated protein kinase 2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of MAPKAPK2More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of MAPK2More data for this Ligand-Target Pair
TargetTyrosine-protein kinase ABL1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Abl kinaseMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKBgammaMore data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKBbetaMore data for this Ligand-Target Pair
TargetPlatelet-derived growth factor receptor alpha(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PDGFRalphaMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 11(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of SAPK2betaMore data for this Ligand-Target Pair
TargetDual specificity mitogen-activated protein kinase kinase 4(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of MKK4More data for this Ligand-Target Pair
TargetCyclin-dependent kinase 6(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
TargetSerine/threonine-protein kinase N2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PRK2More data for this Ligand-Target Pair
TargetDual specificity mitogen-activated protein kinase kinase 6(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of MKK6More data for this Ligand-Target Pair
TargetProtein kinase C iota type(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKCiotaMore data for this Ligand-Target Pair
TargetInsulin-like growth factor 1 receptor(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of IGF1RMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 8(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of JNK1alpha1More data for this Ligand-Target Pair
TargetFibroblast growth factor receptor 2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of FGFR2More data for this Ligand-Target Pair
TargetTyrosine-protein kinase SYK(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of SykMore data for this Ligand-Target Pair
TargetTyrosine-protein kinase receptor UFO(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Axl kinaseMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 12(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of SAPK3More data for this Ligand-Target Pair
TargetDual specificity mitogen-activated protein kinase kinase 1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of MEK1More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Chk1More data for this Ligand-Target Pair
TargetProtein kinase C epsilon type(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKCepsilonMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 3(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of ERK1More data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase D1(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of PKCmuMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 9(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of JNK2alpha2More data for this Ligand-Target Pair
TargetTyrosine-protein kinase Blk(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of Blk kinaseMore data for this Ligand-Target Pair
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of IKK-betaMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 10(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of JNK3More data for this Ligand-Target Pair
TargetTyrosine-protein kinase CSK(Homo sapiens (Human))
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Banyu Tsukuba Research Institute in collaboration with Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of CSKMore data for this Ligand-Target Pair