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Found 110 with Last Name = 'francisco' and Initial = 'gd'
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50047247(1,3-Dibutyl-7-(2-oxo-propyl)-3,7-dihydro-purine-2,...)
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
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473208(CHEMBL20531)
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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473209(CHEMBL20958)
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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473206(CHEMBL20951)
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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473212(CHEMBL418740)
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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473211(CHEMBL282923)
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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076683(CHEMBL6533 | Sodium; (2S,3S,5R,6R)-6-hydroxymethyl...)
Affinity DataIC50:  6nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076678((2S,5R,6R)-6-Hydroxymethyl-3,3-dimethyl-4,4,7-trio...)
Affinity DataIC50:  8nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076681(CHEMBL6469 | Sodium; (2S,3S,5R,6R)-3-((Z)-2-cyano-...)
Affinity DataIC50:  19nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473210(CHEMBL20822)
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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473207(CHEMBL418371)
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
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50403733(CHEMBL1206880 | CL-191121)
Affinity DataIC50:  35nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076680(CHEMBL6461 | Ro-48-1220 | Sodium; (2S,3R,5R)-3-((Z...)
Affinity DataIC50:  42nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50157692(CHEMBL1439 | CL-307579 | Sodium; (2S,3S,5R)-3-meth...)
Affinity DataIC50:  60nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50157692(CHEMBL1439 | CL-307579 | Sodium; (2S,3S,5R)-3-meth...)
Affinity DataIC50:  60nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076682(CHEMBL6678 | Sodium; (2S,3S,5R,6R)-6-hydroxymethyl...)
Affinity DataIC50:  64nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076671((4R,6S)-3-{(2R,3R)-2-[((S)-1-Carboxy-2-methyl-prop...)
Affinity DataIC50:  68nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076679(CHEMBL269471 | Sodium; (2S,3S,5R,6R)-3-((E)-2-cyan...)
Affinity DataIC50:  74nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076671((4R,6S)-3-{(2R,3R)-2-[((S)-1-Carboxy-2-methyl-prop...)
Affinity DataIC50:  91nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076673(CHEMBL175189 | Sodium; (2S,5R,6R)-6-((S)-1-hydroxy...)
Affinity DataIC50:  120nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50047247(1,3-Dibutyl-7-(2-oxo-propyl)-3,7-dihydro-purine-2,...)
Affinity DataIC50:  170nMAssay Description:Inhibition of phosphodiesterase 4 (PDE4)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50403733(CHEMBL1206880 | CL-191121)
Affinity DataIC50:  180nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076681(CHEMBL6469 | Sodium; (2S,3S,5R,6R)-3-((Z)-2-cyano-...)
Affinity DataIC50:  270nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076679(CHEMBL269471 | Sodium; (2S,3S,5R,6R)-3-((E)-2-cyan...)
Affinity DataIC50:  280nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076682(CHEMBL6678 | Sodium; (2S,3S,5R,6R)-6-hydroxymethyl...)
Affinity DataIC50:  280nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076683(CHEMBL6533 | Sodium; (2S,3S,5R,6R)-6-hydroxymethyl...)
Affinity DataIC50:  360nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076680(CHEMBL6461 | Ro-48-1220 | Sodium; (2S,3R,5R)-3-((Z...)
Affinity DataIC50:  1.13E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076678((2S,5R,6R)-6-Hydroxymethyl-3,3-dimethyl-4,4,7-trio...)
Affinity DataIC50:  1.16E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50021954((2S,5R)-3,3-Dimethyl-4,4,7-trioxo-4lambda*6*-thia-...)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50021954((2S,5R)-3,3-Dimethyl-4,4,7-trioxo-4lambda*6*-thia-...)
Affinity DataIC50:  1.40E+3nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076674(CHEMBL177772 | Sodium; (2S,5R,6S)-6-((S)-1-hydroxy...)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473687(CHEMBL76024)
Affinity DataIC50:  4.90E+3nMAssay Description:Inhibition of phosphodiesterase 4 (PDE4)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4A/4B/4C/4D(Homo sapiens (Human))
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50473688(CHEMBL77858)
Affinity DataIC50:  4.90E+3nMAssay Description:Inhibition of phosphodiesterase 4 (PDE4)More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076672((2S,5R,6S)-6-Hydroxymethyl-3,3-dimethyl-4,4,7-trio...)
Affinity DataIC50:  5.80E+3nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076672((2S,5R,6S)-6-Hydroxymethyl-3,3-dimethyl-4,4,7-trio...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetBeta-lactamase(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076677(CHEMBL177912 | Sodium; (2S,5R,6S)-6-((R)-1-hydroxy...)
Affinity DataIC50:  1.02E+4nMAssay Description:Inhibitory activity of the compound against AmpC (class C) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221037(CHEMBL87262)
Affinity DataIC50:  1.21E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221030(CHEMBL313078)
Affinity DataIC50:  2.12E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221032(CHEMBL86526)
Affinity DataIC50:  2.35E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylmuramate--L-alanine ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221038(CHEMBL87521)
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
In DepthDetails ArticlePubMed
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221018(CHEMBL85772)
Affinity DataIC50:  2.80E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221037(CHEMBL87262)
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
In DepthDetails ArticlePubMed
TargetBeta-lactamase TEM(Escherichia coli)
Wyeth-Ayerst Research

Curated by ChEMBL
LigandPNGBDBM50076675(CHEMBL265722 | Sodium; (2S,5R,6R)-6-hydroxymethyl-...)
Affinity DataIC50:  3.10E+4nMAssay Description:Inhibitory activity of the compound against TEM-1 (class A) beta-lactamaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221022(CHEMBL86525)
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
In DepthDetails ArticlePubMed
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221025(CHEMBL83021)
Affinity DataIC50:  3.34E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221032(CHEMBL86526)
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
In DepthDetails ArticlePubMed
TargetUDP-N-acetylmuramoylalanine--D-glutamate ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221030(CHEMBL313078)
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
In DepthDetails ArticlePubMed
TargetUDP-N-acetylmuramate--L-alanine ligase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221037(CHEMBL87262)
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
In DepthDetails ArticlePubMed
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221038(CHEMBL87521)
Affinity DataIC50:  3.83E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUDP-N-acetylenolpyruvoylglucosamine reductase(Staphylococcus aureus (Firmicutes))
Wyeth Research

Curated by ChEMBL
LigandPNGBDBM50221020(CHEMBL87126)
Affinity DataIC50:  3.84E+4nMAssay Description:In vitro inhibitory activity against Staphylococcus aureus UDP-N-acetylmuramate dehydrogenaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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