Compile Data Set for Download or QSAR
Found 55 with Last Name = 'niijima' and Initial = 'j'
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 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 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 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
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
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 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 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
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
TargetAdenosine receptor A2b(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 DataIC50: 14nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50079652((E)-1-[(R)-2-(2-Hydroxy-ethyl)-piperidin-1-yl]-3-(...)copy SMILEScopy InChI
Affinity DataIC50: 17.2nMAssay Description:Inhibitory activity against cyclic AMP production in rat Adenosine A1 receptor assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 23nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 49nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50006710(8-[(E)-2-(3,4-Dimethoxy-phenyl)-vinyl]-7-methyl-1,...)copy SMILEScopy InChI
Affinity DataIC50: 62nMAssay Description:Inhibitory activity against cyclic AMP production in rat Adenosine A1 receptor assayMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 63nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095787(3-[6-Amino-2-(1-hydroxy-cyclohexylethynyl)-9-methy...)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 77nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 140nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 150nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095782(1-[6-Amino-8-(4-fluoro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM82015(1,3-Dimethyl-8-phenyl-3,9-dihydro-purine-2,6-dione...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM82015(1,3-Dimethyl-8-phenyl-3,9-dihydro-purine-2,6-dione...)copy SMILEScopy InChI
Affinity DataIC50: 415nMAssay Description:Inhibitory activity against cyclic AMP production in human Adenosine A2B receptor assayMore 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
LigandPNGBDBM82015(1,3-Dimethyl-8-phenyl-3,9-dihydro-purine-2,6-dione...)copy SMILEScopy InChI
Affinity DataIC50: 454nMAssay 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
TargetAdenosine receptor A2b(Homo sapiens (Human))
Eisai Company, Ltd.

Curated by ChEMBL
LigandPNGBDBM50095779(1-[6-Amino-8-(4-chloro-phenyl)-9-methyl-9H-purin-2...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 980nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore 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
LigandPNGBDBM82015(1,3-Dimethyl-8-phenyl-3,9-dihydro-purine-2,6-dione...)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+3nMAssay Description:Inhibitory activity against cyclic AMP production in human adenosine A3 receptor assayMore 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
LigandPNGBDBM82015(1,3-Dimethyl-8-phenyl-3,9-dihydro-purine-2,6-dione...)copy SMILEScopy InChI
Affinity DataIC50: 1.34E+3nMAssay Description:Binding Affinity for Adenosine A1 receptor expressed in CHO-K1 cells compared to [3H]-CCPAMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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: 1.50E+3nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
TargetAdenosine receptor A2b(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 DataIC50: 3.00E+3nMAssay Description:Inhibitory activity on NECA-induced cyclic-AMP accumulation in CHO-K1 cells expressing human Adenosine A2B receptorMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2R49Q0XPubMed
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