TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 0.170nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 1.20nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 1.30nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 3.20nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 4.10nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 6nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
Affinity DataIC50: 6nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 8nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 19nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 23nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 25nMAssay Description:Concentration at which 50% of the activity of the Phosphodiesterase 4 from Human U937 cells is inhibitedMore data for this Ligand-Target Pair
Affinity DataIC50: 35nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 42nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 60nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 60nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 64nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 68nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 74nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 91nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 120nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 170nMAssay Description:Inhibition of phosphodiesterase 4 (PDE4)More data for this Ligand-Target Pair
Affinity DataIC50: 180nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 270nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 280nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 280nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 360nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.13E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.16E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of phosphodiesterase 4 (PDE4)More data for this Ligand-Target Pair
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research
Curated by ChEMBL
Wyeth-Ayerst Research
Curated by ChEMBL
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of phosphodiesterase 4 (PDE4)More data for this Ligand-Target Pair
Affinity DataIC50: 5.80E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
Affinity DataIC50: 1.02E+4nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 1.21E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 2.12E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 2.35E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylmuramate--L-alanine ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 2.43E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramoyl-L-alanine synthetaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 2.80E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.02E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramoyl-L-alanyl-D-glutamate synthetaseMore data for this Ligand-Target Pair
Affinity DataIC50: 3.10E+4nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.28E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramoyl-L-alanyl-D-glutamate synthetaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.34E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.45E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramoyl-L-alanyl-D-glutamate synthetaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.60E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramoyl-L-alanyl-D-glutamate synthetaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylmuramate--L-alanine ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.70E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramoyl-L-alanine synthetaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.83E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research
Curated by ChEMBL
Wyeth Research
Curated by ChEMBL
Affinity DataIC50: 3.84E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair