Compile Data Set for Download or QSAR
Found 429 with Last Name = 'murakami' and Initial = 'm'
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095778(4-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  9.10nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095790(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  9.80nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095786(1-(6-Amino-8-furan-2-yl-9-methyl-9H-purin-2-ylethy...)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095787(3-[6-Amino-2-(1-hydroxy-cyclohexylethynyl)-9-methy...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50059376(9-Methyl-2-phenyl-5,9-dihydro-[1,2,4]triazolo[5,1-...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Binding affinity towards adenosine A3 receptor expressed in HEK-293 cells versus [125I]-AB-MECAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095784(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095793(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  14nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095788(1-[6-Amino-8-(2-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  15nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095793(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50079652((E)-1-[(R)-2-(2-Hydroxy-ethyl)-piperidin-1-yl]-3-(...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095788(1-[6-Amino-8-(2-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  19nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095781(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  19nMAssay Description:Binding Affinity towards Adenosine A2A receptor expressed in HEK-293 cells versus [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095790(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095786(1-(6-Amino-8-furan-2-yl-9-methyl-9H-purin-2-ylethy...)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095781(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  27nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095784(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  29nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095778(4-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50006710(8-[(E)-2-(3,4-Dimethoxy-phenyl)-vinyl]-7-methyl-1,...)copy SMILEScopy InChI
Affinity DataKi:  71nMAssay Description:Binding Affinity for adenosine A2A receptor expressed in HEK-293 cells compared to [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095787(3-[6-Amino-2-(1-hydroxy-cyclohexylethynyl)-9-methy...)copy SMILEScopy InChI
Affinity DataKi:  130nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50603613(CHEMBL5169644)copy SMILES
Affinity DataKi:  210nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6QGPPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095784(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  330nMAssay Description:Binding affinity towards adenosine A3 receptor expressed in HEK-293 cells versus [125I]-AB-MECAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50603613(CHEMBL5169644)copy SMILES
Affinity DataKi:  483nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6QGPPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095793(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  540nMAssay Description:Binding affinity towards adenosine A3 receptor expressed in HEK-293 cells versus [125I]-AB-MECAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095790(1-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  1.10E+3nMAssay Description:Binding affinity towards adenosine A3 receptor expressed in HEK-293 cells versus [125I]-AB-MECAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50079652((E)-1-[(R)-2-(2-Hydroxy-ethyl)-piperidin-1-yl]-3-(...)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:Binding Affinity for adenosine A2A receptor expressed in HEK-293 cells compared to [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095778(4-[6-Amino-8-(3-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataKi:  2.10E+3nMAssay Description:Binding affinity towards adenosine A3 receptor expressed in HEK-293 cells versus [125I]-AB-MECAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50006710(8-[(E)-2-(3,4-Dimethoxy-phenyl)-vinyl]-7-methyl-1,...)copy SMILEScopy InChI
Affinity DataKi:  2.50E+3nMAssay Description:Binding affinity towards adenosine A3 receptor expressed in HEK-293 cells versus [125I]-AB-MECAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50079652((E)-1-[(R)-2-(2-Hydroxy-ethyl)-piperidin-1-yl]-3-(...)copy SMILEScopy InChI
Affinity DataKi:  2.80E+3nMAssay Description:Binding affinity towards adenosine A3 receptor expressed in HEK-293 cells versus [125I]-AB-MECAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50603612(CHEMBL5171777)copy SMILES
Affinity DataKi:  6.82E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6QGPPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50059376(9-Methyl-2-phenyl-5,9-dihydro-[1,2,4]triazolo[5,1-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50006710(8-[(E)-2-(3,4-Dimethoxy-phenyl)-vinyl]-7-methyl-1,...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding Affinity towards Adenosine A1 receptor expressed in CHO-K1 cells versus [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50059376(9-Methyl-2-phenyl-5,9-dihydro-[1,2,4]triazolo[5,1-...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Binding Affinity for adenosine A2A receptor expressed in HEK-293 cells compared to [3H]-CGS-21,680More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A3(Mus musculus)TBA
LigandPNGBDBM50603613(CHEMBL5169644)copy SMILES
Affinity DataKi: >1.00E+4nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PV6QGPPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035609(CHEMBL3338455)copy SMILEScopy InChI
Affinity DataIC50: 0.0530nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetHigh affinity nerve growth factor receptor(Homo sapiens (Human))
Takeda Pharmaceutical Company Limited

Curated by ChEMBL
LigandPNGBDBM50524981(CHEMBL4562879)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of N-terminal GST-tagged human TrkA kinase domain (436 to 790 residues) expressed in baculovirus expression system using biotin-poly-GT as...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B56P57PubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035620(CHEMBL3338445)copy SMILEScopy InChI
Affinity DataIC50: 0.130nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035617(CHEMBL3338448)copy SMILEScopy InChI
Affinity DataIC50: 0.380nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035621(CHEMBL3338444)copy SMILEScopy InChI
Affinity DataIC50: 0.660nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035613(CHEMBL3338452)copy SMILEScopy InChI
Affinity DataIC50: 0.740nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50036633(CHEMBL3354285)copy SMILEScopy InChI
Affinity DataIC50: 0.900nMAssay Description:Inhibition of dog lungs PDE5 using [3H]cGMP as substrate after 30 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JS9S1WPubMed
TargetAdenosine receptor A2a(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50006710(8-[(E)-2-(3,4-Dimethoxy-phenyl)-vinyl]-7-methyl-1,...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibitory activity against cyclic AMP production in rat Adenosine A2A receptor assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Homo sapiens (Human))
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50100662(CHEMBL553371 | CHEMBL77971 | methyl 2-(4-aminophen...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of PDE5 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50036625(CHEMBL3354279)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of dog lungs PDE5 using [3H]cGMP as substrate after 30 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JS9S1WPubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Takeda Pharmaceutical Company Limited

Curated by ChEMBL
LigandPNGBDBM50524985(CHEMBL4460367)copy SMILEScopy InChI
Affinity DataIC50: 1.20nMAssay Description:Inhibition of human ALK kinase domain (1058 to 1620 residues) expressed in baculovirus expression system using biotin-poly-GT as substrate pre-incuba...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B56P57PubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035611(CHEMBL3338453)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035618(CHEMBL3338447)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Homo sapiens (Human))
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM14390(5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phen...)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Inhibition of PDE5 (unknown origin)More data for this Ligand-Target Pair
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50035615(CHEMBL3338450)copy SMILEScopy InChI
Affinity DataIC50: 1.70nMAssay Description:Inhibition of canine lung PDE5 using [3H]cGMP substrate by radiolabeled nucleotide methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76F5ZPubMed
TargetALK tyrosine kinase receptor(Homo sapiens (Human))
Takeda Pharmaceutical Company Limited

Curated by ChEMBL
LigandPNGBDBM50306682((R)-3-(1-(2,6-dichloro-3-fluorophenyl)ethoxy)-5-(1...)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of human ALK kinase domain (1058 to 1620 residues) expressed in baculovirus expression system using biotin-poly-GT as substrate pre-incuba...More data for this Ligand-Target Pair
TargetcGMP-specific 3',5'-cyclic phosphodiesterase(Canis lupus familiaris)
Mitsubishi Tanabe Pharma Corporation

Curated by ChEMBL
LigandPNGBDBM50036632(CHEMBL3354284)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of dog lungs PDE5 using [3H]cGMP as substrate after 30 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2JS9S1WPubMed
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