Compile Data Set for Download or QSAR
Report error Found 27 Enz. Inhib. hit(s) with all data for entry = 50040617
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397056BDBM50397056(CHEMBL2171440)
Affinity DataIC50: 3nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397053BDBM50397053(CHEMBL2171422)
Affinity DataIC50: 11nMAssay Description:Inhibition of cloned human recombinant PDE7B assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397052BDBM50397052(CHEMBL2171423)
Affinity DataIC50: 12nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397061BDBM50397061(CHEMBL2171435)
Affinity DataIC50: 18nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397052BDBM50397052(CHEMBL2171423)
Affinity DataIC50: 19nMAssay Description:Inhibition of cloned human recombinant PDE7B assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397060BDBM50397060(CHEMBL2171436)
Affinity DataIC50: 24nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397053BDBM50397053(CHEMBL2171422)
Affinity DataIC50: 27nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397054BDBM50397054(CHEMBL2171421)
Affinity DataIC50: 31nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397062BDBM50397062(CHEMBL2171434)
Affinity DataIC50: 32nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397063BDBM50397063(CHEMBL2171433)
Affinity DataIC50: 33nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 7B(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397054BDBM50397054(CHEMBL2171421)
Affinity DataIC50: 43nMAssay Description:Inhibition of cloned human recombinant PDE7B assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397067BDBM50397067(CHEMBL2171429)
Affinity DataIC50: 45nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397066BDBM50397066(CHEMBL2171430)
Affinity DataIC50: 53nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397068BDBM50397068(CHEMBL2171428)
Affinity DataIC50: 55nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Mouse)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397054BDBM50397054(CHEMBL2171421)
Affinity DataIC50: 63nMAssay Description:Inhibition of mouse PDE7A assessed as [3H]cAMP hydrolysis after 5 to 15 mins by scintillation counterMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397059BDBM50397059(CHEMBL2171437)
Affinity DataIC50: 68nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397065BDBM50397065(CHEMBL2171431)
Affinity DataIC50: 71nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397069BDBM50397069(CHEMBL2171427)
Affinity DataIC50: 73nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397055BDBM50397055(CHEMBL2171442)
Affinity DataIC50: 75nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397072BDBM50397072(CHEMBL2171426)
Affinity DataIC50: 77nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397071BDBM50397071(CHEMBL2171425)
Affinity DataIC50: 80nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397064BDBM50397064(CHEMBL2171432)
Affinity DataIC50: 81nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397058BDBM50397058(CHEMBL2171438)
Affinity DataIC50: 89nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397057BDBM50397057(CHEMBL2171439)
Affinity DataIC50: 93nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHigh affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397070BDBM50397070(CHEMBL2171424)
Affinity DataIC50: 104nMAssay Description:Inhibition of cloned human recombinant PDE7A assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4D(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397052BDBM50397052(CHEMBL2171423)
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of cloned human recombinant PDE4D assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetcAMP-specific 3',5'-cyclic phosphodiesterase 4D(Human)
Glenmark Pharmaceuticals

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50397054BDBM50397054(CHEMBL2171421)
Affinity DataIC50: 6.55E+3nMAssay Description:Inhibition of cloned human recombinant PDE4D assessed as [3H]cAMP hydrolysis by radiometric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed