Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: >10nMAssay Description:Binding affinity towards human cloned 5-hydroxytryptamine 1A receptor using [3H]-8-OH-DPAT as radioligandMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: <1.00E+3nMAssay Description:Tested for inhibition of substrate hydrolysis in the presence of porcine kidney esterase at a concentration of 1 uMMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: >1.80E+3nMAssay Description:Ability to displace [3H]5-CT (2.0 nM) from HeLa cells of human 5-hydroxytryptamine 1A receptorMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
University Of Camerino
Curated by ChEMBL
University Of Camerino
Curated by ChEMBL
Affinity DataKi: 2.34E+3nMAssay Description:Binding affinity against native 5-HT1A-receptors from rat hippocampus using radioligand ([3H]8-hydroxy-2-(di-n-propylamino)-tetraline) binding assayMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Rattus norvegicus (rat))
University Of Camerino
Curated by ChEMBL
University Of Camerino
Curated by ChEMBL
Affinity DataKi: 2.36E+3nMAssay Description:The compound was tested for binding affinity on [3H]-8-OH-DPAT as specific ligand on 5-hydroxytryptamine 1A receptor in rat hippocampusMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1A(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL