Compile Data Set for Download or QSAR
Report error Found 20 Enz. Inhib. hit(s) with all data for entry = 50048128
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205604BDBM50205604(CHEMBL3907401)
Affinity DataIC50: 170nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205613BDBM50205613(CHEMBL3934464)
Affinity DataIC50: 260nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205599BDBM50205599(CHEMBL3933197)
Affinity DataIC50: 290nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205619BDBM50205619(CHEMBL3965269)
Affinity DataIC50: 320nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205603BDBM50205603(CHEMBL3937306)
Affinity DataIC50: 340nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205600BDBM50205600(CHEMBL3897315)
Affinity DataIC50: 1.13E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205614BDBM50205614(CHEMBL3892849)
Affinity DataIC50: 1.22E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205602BDBM50205602(CHEMBL3919202)
Affinity DataIC50: 1.22E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205610BDBM50205610(CHEMBL3926566)
Affinity DataIC50: 1.22E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205611BDBM50205611(CHEMBL3969575)
Affinity DataIC50: 1.29E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 14769BDBM14769(6-[4-(difluoromethoxy)-3-methoxyphenyl]-2,3-dihydr...)
Affinity DataIC50: 1.41E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMedPDB3D3D Structure (crystal)
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205608BDBM50205608(CHEMBL3898376)
Affinity DataIC50: 1.41E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205617BDBM50205617(CHEMBL3916376)
Affinity DataIC50: 2.27E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205609BDBM50205609(CHEMBL3938207)
Affinity DataIC50: 2.69E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205618BDBM50205618(CHEMBL3929714)
Affinity DataIC50: 3.53E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205605BDBM50205605(CHEMBL3932749)
Affinity DataIC50: 3.53E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205601BDBM50205601(CHEMBL3892468)
Affinity DataIC50: 4.17E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205607BDBM50205607(CHEMBL3925358)
Affinity DataIC50: 7.55E+3nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205612BDBM50205612(CHEMBL3910284)
Affinity DataIC50: 1.31E+4nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4B(Human)
University of Genoa

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50205606BDBM50205606(CHEMBL3945980)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of human recombinant PDE4B2 using cAMP as substrate after 2 hrs by TR-FRET assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/20/2018
Entry Details Article
PubMed