Compile Data Set for Download or QSAR
Found 150 Enz. Inhib. hit(s) with all data for entry = 50018243
LigandPNGBDBM50408387(CHEMBL5268482)copy SMILEScopy InChI
Affinity DataIC50: 0.0400nMAssay Description:Antagonist activity at human P2X7 receptor transfected in THP1 cells assessed as inhibition of benzoyl-ATP-induced changes in plasma membrane pore fo...More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50408386(CHEMBL5287343)copy SMILEScopy InChI
Affinity DataIC50: 0.260nMAssay Description:Antagonist activity at human P2X7 receptor transfected in THP1 cells assessed as inhibition of benzoyl-ATP-induced changes in plasma membrane pore fo...More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50411638(CHEMBL404371)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Antagonist activity at human P2X7 receptor transfected in THP1 cells assessed as inhibition of benzoyl-ATP-induced changes in plasma membrane pore fo...More data for this Ligand-Target Pair
In DepthDetails
TargetPoly [ADP-ribose] polymerase 2(Homo sapiens (Human))TBA
LigandPNGBDBM50446130(AG-014699 | AG-14447 | RUCAPARIB CAMSYLATE | Rucap...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Antagonist activity at human P2X7 receptor transfected in THP1 cells assessed as inhibition of benzoyl-ATP-induced changes in plasma membrane pore fo...More data for this Ligand-Target Pair
In DepthDetails
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50446130(AG-014699 | AG-14447 | RUCAPARIB CAMSYLATE | Rucap...)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Antagonist activity at human P2X7 receptor transfected in THP1 cells assessed as inhibition of benzoyl-ATP-induced changes in plasma membrane pore fo...More data for this Ligand-Target Pair
TargetGlycogen synthase kinase-3 alpha(Homo sapiens (Human))TBA
LigandPNGBDBM7262(14-nitro-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
TargetGlycogen synthase kinase-3 beta(Rattus norvegicus (rat))TBA
LigandPNGBDBM7262(14-nitro-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM7262(14-nitro-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 4.5nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))TBA
LigandPNGBDBM50256044(5-(2-amino-4-oxo-1H-imidazol-5(4H)-ylidene)-2,3,4,...)copy SMILEScopy InChI
Affinity DataIC50: 8nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
TargetMitogen-activated protein kinase 1(Homo sapiens (Human))TBA
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 9nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
TargetGlycogen synthase kinase-3 beta(Rattus norvegicus (rat))TBA
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50408186(CHEMBL5272006)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Antagonist activity at rat UT receptorMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50408185(CHEMBL5265856)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Antagonist activity at rat UT receptorMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))TBA
LigandPNGBDBM50256003(4-[2-Amino-5-oxo-3,5-dihydro-imidazol-(4)-ylidene]...)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))TBA
LigandPNGBDBM50363648(CHEMBL1947252)copy SMILEScopy InChI
Affinity DataIC50: 14nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM7262(14-nitro-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationMore data for this Ligand-Target Pair
In DepthDetails
TargetGlycogen synthase kinase-3 beta(Rattus norvegicus (rat))TBA
LigandPNGBDBM2579((2S,3R,4R,6R)-3-methoxy-2-methyl-4-(methylamino)-2...)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))TBA
LigandPNGBDBM50363646(CHEMBL1947250)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
TargetMitogen-activated protein kinase 3(Homo sapiens (Human))TBA
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Antagonist effect against 2-methyl-5-HT activity at 5-HT3 receptor in longitudinal muscle myenteric plexus from guinea pig ileumMore data for this Ligand-Target Pair
In DepthDetails
TargetMitogen-activated protein kinase 3(Homo sapiens (Human))TBA
LigandPNGBDBM7262(14-nitro-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
TargetGlycogen synthase kinase-3 beta(Rattus norvegicus (rat))TBA
LigandPNGBDBM50166289(CHEBI:43645 | CHEMBL216543)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
TargetGlycogen synthase kinase-3 beta(Rattus norvegicus (rat))TBA
LigandPNGBDBM7266(14-bromo-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM7263(9-cyanopaullone | 9-oxo-8,18-diazatetracyclo[9.7.0...)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM7263(9-cyanopaullone | 9-oxo-8,18-diazatetracyclo[9.7.0...)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:Antagonist activity at human M3 receptor assessed as inhibition of carbachol bindingMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
TargetProtein mono-ADP-ribosyltransferase PARP3(Homo sapiens (Human))TBA
LigandPNGBDBM50446130(AG-014699 | AG-14447 | RUCAPARIB CAMSYLATE | Rucap...)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:Antagonist activity at rat P2X7 receptor transfected in HEK cells assessed as inhibition of benzylATP-induced changes in plasma membrane pore formati...More data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))TBA
LigandPNGBDBM50363649(CHEMBL1947253)copy SMILEScopy InChI
Affinity DataIC50: 28nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))TBA
LigandPNGBDBM50256004(4-[2-Amino-5-oxo-3,5-dihydro-imidazol-(4)-ylidene]...)copy SMILEScopy InChI
Affinity DataIC50: 29nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM7262(14-nitro-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationMore data for this Ligand-Target Pair
In DepthDetails
TargetGlycogen synthase kinase-3 beta(Rattus norvegicus (rat))TBA
LigandPNGBDBM50408385(CHEMBL5280328)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM7262(14-nitro-8,18-diazatetracyclo[9.7.0.0^{2,7}.0^{12,...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Antagonist activity at rat UT receptorMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))TBA
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 42nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50256043((Z)-3-bromohymenialdisine | CHEMBL480350 | Hymenia...)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50408140(CHEMBL1233473)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:Activity at human B2 receptor transfected in CHO cells assessed as ability to antagonize BK-induced inositol-phosphate accumulationMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50408184(CHEMBL5280645)copy SMILEScopy InChI
Affinity DataIC50: 75nMAssay Description:Antagonist activity at muscarinic receptor M2 assessed as contraction of electrically-stimulated guinea pig left atriaMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50408177(CHEMBL5271328)copy SMILEScopy InChI
Affinity DataIC50: 79nMAssay Description:Antagonist potency on BK-induced contraction of guinea pig ileum longitudinal smooth muscleMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk1(Homo sapiens (Human))TBA
LigandPNGBDBM50256043((Z)-3-bromohymenialdisine | CHEMBL480350 | Hymenia...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50259155((Z)-Hymenialdisine | Hymenialdisine)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50363645(DEBROMOHYMENIALDISINE)copy SMILEScopy InChI
Affinity DataIC50: 112nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50363645(DEBROMOHYMENIALDISINE)copy SMILEScopy InChI
Affinity DataIC50: 112nMAssay Description:Antagonist potency at human bradykinin B2 receptor assessed as effect on inositol monophosphate accumulation in CHOdhfr- cellsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM7336(13-bromo-3-thia-7,17-diazatetracyclo[8.7.0.0^{2,6}...)copy SMILEScopy InChI
Affinity DataIC50: 120nMAssay Description:Antagonist activity against adrenergic alpha-1A receptor in rat prostatic vas deferens assessed as inhibition of noradrenaline-induced contractionMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))TBA
LigandPNGBDBM50363653(CHEMBL1944822)copy SMILEScopy InChI
Affinity DataIC50: 156nMAssay Description:Antagonist activity in rat uterus by uterotonic assayMore data for this Ligand-Target Pair
In DepthDetails
TargetSerine/threonine-protein kinase Chk2(Homo sapiens (Human))TBA
LigandPNGBDBM50363654(CHEMBL1944823)copy SMILEScopy InChI
Affinity DataIC50: 171nMAssay Description:Antagonist activity in phenoxybenzamine-treated rat by Pressor assayMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50408182(CHEMBL5285766)copy SMILEScopy InChI
Affinity DataIC50: 177nMAssay Description:Antagonist activity at putative muscarinic receptor M4 assessed as contraction of electrically-stimulated guinea pig lung stripsMore data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50256044(5-(2-amino-4-oxo-1H-imidazol-5(4H)-ylidene)-2,3,4,...)copy SMILEScopy InChI
Affinity DataIC50: 177nMAssay Description:Antagonist activity at muscarinic receptor M2 assessed as contraction of electrically-stimulated guinea pig left atriaMore data for this Ligand-Target Pair
In DepthDetails
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