Compile Data Set for Download or QSAR
Report error Found 80 Enz. Inhib. hit(s) with all data for entry = 50031786
LigandChemical structure of BindingDB Monomer ID 31592BDBM31592(PF-2545920 | substituted pyrazole, 9 | US9138494, ...)
Affinity DataIC50: 1.30nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319169BDBM50319169(3,4-Dimethoxy-1-isobutyl-8-methoxy-imidazo[1,5-a]p...)
Affinity DataIC50: 1.40nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319168BDBM50319168(1-Cyclohexyl-3,4-dimethyl-8-methoxy-imidazo[1,5-a]...)
Affinity DataIC50: 2.80nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319163BDBM50319163(8-Methoxy-3-methyl-4-methylsulfonylamino-1-propyl-...)
Affinity DataIC50: 7.20nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMedPDB3D3D Structure (crystal)
LigandChemical structure of BindingDB Monomer ID 50319165BDBM50319165(2-methoxy-6,7-dimethyl-9-propylimidazo[1,5-a]pyrid...)
Affinity DataIC50: 7.30nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319164BDBM50319164(4-Difluoromethyl-8-methoxy-3-methyl-1-propyl-imida...)
Affinity DataIC50: 7.30nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319166BDBM50319166(1-Propyl-3,4,8-trimethyl-imidazo[1,5-a]pyrido[3,2-...)
Affinity DataIC50: 8.30nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319159BDBM50319159(4-Cyano-1-cyclohexyl-8-methoxy-3-methyl-imidazo[1,...)
Affinity DataIC50: 9.60nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319157BDBM50319157(4-Cyano-8-methoxy-3-methyl-1-propyl-imidazo[1,5-a]...)
Affinity DataIC50: 11nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMedPDB3D3D Structure (crystal)
LigandChemical structure of BindingDB Monomer ID 50319160BDBM50319160(4-Ethyl-8-methoxy-3-methyl-1-propyl-imidazo[1,5-a]...)
Affinity DataIC50: 12nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319162BDBM50319162(8-Difluoromethoxy-3,4-dimethyl-1-propyl-imidazo[1,...)
Affinity DataIC50: 13nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319161BDBM50319161(4-(N,N-bis-methylsulfonyl)-8-methoxy-3-methyl-1-pr...)
Affinity DataIC50: 15nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319167BDBM50319167(3,4-Dimethyl-1-ethyl-8-methoxy-imidazo[1,5-a]pyrid...)
Affinity DataIC50: 16nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319152BDBM50319152(1-Benzyl-3,4-dimethyl-8-methoxy-imidazo[1,5-a]pyri...)
Affinity DataIC50: 21nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319158BDBM50319158(8-Methoxy-3-methyl-4-methylsulfonyl-1-propyl-imida...)
Affinity DataIC50: 23nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319155BDBM50319155(8-Methoxy-4-methoxycarbonylamino-3-methyl-1-propyl...)
Affinity DataIC50: 23nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319149BDBM50319149(4,8-Dimethoxy-3-methyl-1-propyl-imidazo[1,5-a]pyri...)
Affinity DataIC50: 25nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319156BDBM50319156(8-Methoxy-4-methyl-1-propyl-imidazo[1,5-a]pyrido[3...)
Affinity DataIC50: 25nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319148BDBM50319148(3,4-Dimethyl-1-propyl-imidazo[1,5-a]pyrido[3,2-e]p...)
Affinity DataIC50: 33nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319186BDBM50319186(8-Methoxy-3-methyl-1-propyl-imidazo[1,5-a]pyrido[3...)
Affinity DataIC50: 34nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319185BDBM50319185(4-Cyano-1-ethyl-8-methoxy-3-methyl-imidazo[1,5-a]p...)
Affinity DataIC50: 36nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319154BDBM50319154(4-Ethylsulfonylamino-8-methoxy-3-methyl-1-propyl-i...)
Affinity DataIC50: 39nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319153BDBM50319153(8-Methoxy-3-methyl-1-propyl-4-trifluoromethyl-imid...)
Affinity DataIC50: 46nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319151BDBM50319151(3,4-Dimethyl-8-methoxy-1-pentyl-imidazo[1,5-a]pyri...)
Affinity DataIC50: 51nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319183BDBM50319183(8-Methoxy-3-methyl-1-propyl-4-trifluoromethylsulfo...)
Affinity DataIC50: 53nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319182BDBM50319182(8-Methoxy-3-methyl-1-propyl-4-ureido-imidazo[1,5-a...)
Affinity DataIC50: 55nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 14754BDBM14754(CHEMBL19224 | 1-[(3,4-dimethoxyphenyl)methyl]-6,7-...)
Affinity DataIC50: 56.9nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMedPDB3D3D Structure (crystal)
LigandChemical structure of BindingDB Monomer ID 14754BDBM14754(CHEMBL19224 | 1-[(3,4-dimethoxyphenyl)methyl]-6,7-...)
Affinity DataIC50: 56.9nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMedPDB3D3D Structure (crystal)
LigandChemical structure of BindingDB Monomer ID 50319147BDBM50319147(4,8-Dimethoxy-1-ethyl-3-methyl-imidazo[1,5-a]pyrid...)
Affinity DataIC50: 63nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319187BDBM50319187(1-Ethyl-8-methoxy-3-methyl-4-methylsulfonylamino-i...)
Affinity DataIC50: 65nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
TargetDual 3',5'-cyclic-AMP and -GMP phosphodiesterase 11A(Human)
Biotie Therapies

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50319163BDBM50319163(8-Methoxy-3-methyl-4-methylsulfonylamino-1-propyl-...)
Affinity DataIC50: 69nMAssay Description:Inhibition of PDE11AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319146BDBM50319146(8-Methoxy-1,3,4-trimethyl-imidazo[1,5-a]pyrido[3,2...)
Affinity DataIC50: 81nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319181BDBM50319181(4-(N,N-Bis-ethoxycarbonyl-amino)-8-methoxy-3-methy...)
Affinity DataIC50: 82nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319150BDBM50319150(8-Methoxy-3-methyl-4-methylsulfinyl-1-propyl-imida...)
Affinity DataIC50: 90nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319180BDBM50319180(4,8-Dimethoxy-1-propyl-imidazo[1,5-a]pyrido[3,2-e]...)
Affinity DataIC50: 92nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319177BDBM50319177(8-Methoxy-3,4-dimethyl-1-phenethyl-imidazo[1,5-a]p...)
Affinity DataIC50: 116nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319176BDBM50319176(4-Isopropylsulfonylamino-8-methoxy-3-methyl-1-prop...)
Affinity DataIC50: 132nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319175BDBM50319175(4-Dimethylamino-8-methoxy-3-methyl-1-propyl-imidaz...)
Affinity DataIC50: 146nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319174BDBM50319174(1-Ethyl-8-methoxy-3-methyl-4-propyloxy-imidazo[1,5...)
Affinity DataIC50: 149nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319200BDBM50319200(4-Acetylamino-1-ethyl-8-methoxy-3-methyl-imidazo[1...)
Affinity DataIC50: 175nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319172BDBM50319172(4-Ethoxycarbonylamino-8-methoxy-3-methyl-1-propyl-...)
Affinity DataIC50: 206nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319171BDBM50319171(8-Methoxy-3-methyl-4-methylsulfanyl-1-propyl-imida...)
Affinity DataIC50: 209nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319170BDBM50319170(1-Hexyl-8-methoxy-3,4-dimethyl-imidazo[1,5-a]pyrid...)
Affinity DataIC50: 223nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
TargetcGMP-dependent 3',5'-cyclic phosphodiesterase(Human)
Biotie Therapies

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50319165BDBM50319165(2-methoxy-6,7-dimethyl-9-propylimidazo[1,5-a]pyrid...)
Affinity DataIC50: 239nMAssay Description:Inhibition of PDE2AMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319202BDBM50319202(8-Methoxy-3-methyl-4-methylamino-1-propyl-imidazo[...)
Affinity DataIC50: 246nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319173BDBM50319173(4,8-Dimethoxy-1,3-dimethyl-imidazo[1,5-a]pyrido[3,...)
Affinity DataIC50: 270nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319204BDBM50319204(1-Ethyl-8-methoxy-3-methyl-4-methylsulfinyl-imidaz...)
Affinity DataIC50: 284nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319201BDBM50319201(8-Methoxy-3-methoxycarbonyl-4-methyl-1-propyl-imid...)
Affinity DataIC50: 285nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319184BDBM50319184(3-Ethoxycarbonyl-8-methoxy-4-methyl-1-propyl-imida...)
Affinity DataIC50: 326nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
LigandChemical structure of BindingDB Monomer ID 50319198BDBM50319198(4-(N-Isopropyl-ureido)-8-methoxy-3-methyl-1-propyl...)
Affinity DataIC50: 381nMAssay Description:Inhibition of human recombinant PDE10A expressed in baculovirus-SF21 cell system assessed as hydrolysis of [3H]cAMP after 1 hr by liquid scintillatio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/20/2010
Entry Details Article
PubMed
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