TargetSomatostatin receptor type 2(Homo sapiens (Human))
University of Cambridge
Curated by PDSP Ki Database
University of Cambridge
Curated by PDSP Ki Database
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
Affinity DataKi: 0.126nMAssay Description:Binding affinity against 5-hydroxytryptamine 1D receptor betaMore data for this Ligand-Target Pair
TargetSomatostatin receptor type 5(Homo sapiens (Human))
University of Cambridge
Curated by PDSP Ki Database
University of Cambridge
Curated by PDSP Ki Database
TargetSomatostatin receptor type 1(Homo sapiens (Human))
University of Cambridge
Curated by PDSP Ki Database
University of Cambridge
Curated by PDSP Ki Database
TargetSomatostatin receptor type 3(Homo sapiens (Human))
University of Cambridge
Curated by PDSP Ki Database
University of Cambridge
Curated by PDSP Ki Database
TargetSomatostatin receptor type 4(Homo sapiens (Human))
University of Cambridge
Curated by PDSP Ki Database
University of Cambridge
Curated by PDSP Ki Database
Target5-hydroxytryptamine receptor 1D(Homo sapiens (Human))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
Affinity DataKi: 1.30nMAssay Description:Binding affinity against 5-hydroxytryptamine 1D receptor alphaMore data for this Ligand-Target Pair
TargetSomatostatin receptor type 2(Homo sapiens (Human))
University of Cambridge
Curated by PDSP Ki Database
University of Cambridge
Curated by PDSP Ki Database
Target5-hydroxytryptamine receptor 1B(Rattus norvegicus (Rat))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
Affinity DataKi: 3.20nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
Affinity DataKi: 3.20nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
Affinity DataKi: 3.20nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Rattus norvegicus (Rat))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
Affinity DataKi: 3.20nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1B receptor in rat striatal membrane with [125I]- iodocyanopindololMore data for this Ligand-Target Pair
Affinity DataKi: 4.70nMAssay Description:Tested for its binding affinity at adenosine A1 receptor in rat brain cortical membrane preparations using [3H]-CCPA as a radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 5nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
Affinity DataKi: 5nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 5.10nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Rattus norvegicus (Rat))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
Affinity DataKi: 6.30nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1B receptor in rat striatal membrane with [125I]- iodocyanopindololMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Rattus norvegicus (Rat))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
Affinity DataKi: 6.30nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1B receptor in rat striatal membrane with [125I]- iodocyanopindololMore data for this Ligand-Target Pair
Affinity DataKi: 6.30nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
Affinity DataKi: 6.30nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
Affinity DataKi: 6.70nMAssay Description:Tested for its binding affinity at adenosine A1 receptor in rat brain cortical membrane preparations using [3H]-CCPA as a radioligandMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 8.20nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 8.5nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
Affinity DataKi: 8.80nMAssay Description:Binding affinity against adenosine A1 receptor expressed in CHO cells using [3H]-CCPAMore data for this Ligand-Target Pair
Affinity DataKi: 10nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 13nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 15nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 15nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
Affinity DataKi: 16nMAssay Description:Tested for its binding affinity at adenosine A1 receptor in rat brain cortical membrane preparations using [3H]-CCPA as a radioligandMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 18nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
Affinity DataKi: 19nMAssay Description:Tested for its binding affinity at adenosine A1 receptor in rat brain cortical membrane preparations using [3H]-CCPA as a radioligandMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 24nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 27nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 31nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
Affinity DataKi: 32nMAssay Description:In vitro binding affinity towards 5-hydroxytryptamine 1D receptor in guinea-pig striatum in presence of BMY-7378 and mesulergineMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 35nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 36nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 2A(Rattus norvegicus (rat))
Glaxo Research and Development
Curated by PDSP Ki Database
Glaxo Research and Development
Curated by PDSP Ki Database
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 46nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
Affinity DataKi: 46nMAssay Description:Tested for its binding affinity at adenosine A1 receptor in rat brain cortical membrane preparations using [3H]-CCPA as a radioligandMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 47nMAssay Description:Ability to inhibit binding of [3H]-NECA to Adenosine A2A receptor in rat brain striatal membranesMore data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 61nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 63nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Julius-Maximilians-UniversitäT WüRzburg
Curated by ChEMBL
Affinity DataKi: 68nMAssay Description:Ability to inhibit binding of [3H]-CGS- 21680 to adenosine A2A receptor in rat brain striatal membranes.More data for this Ligand-Target Pair