TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institute
Curated by ChEMBL
Institute
Curated by ChEMBL
Affinity DataKi: 0.0540nMAssay Description:Inhibitory constant for RTX binding to rat spinal cordMore data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Institute
Curated by ChEMBL
Institute
Curated by ChEMBL
Affinity DataKi: 0.120nMAssay Description:Inhibitory constant for RTX binding to porcine spinal cordMore data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Institute
Curated by ChEMBL
Institute
Curated by ChEMBL
Affinity DataKi: 0.450nMAssay Description:Inhibitory constant for RTX binding to human spinal cordMore data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institute
Curated by ChEMBL
Institute
Curated by ChEMBL
Affinity DataKi: 600nMAssay Description:Displacement of [3H]RTX binding from Vanilloid receptor of rat dorsal Root Ganglion (DRG) membranesMore data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Institute
Curated by ChEMBL
Institute
Curated by ChEMBL
Affinity DataKi: 2.00E+3nMAssay Description:Inhibition of [3H]- RTX binding to vanilloid receptor of rat urinary bladderMore data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Institute
Curated by ChEMBL
Institute
Curated by ChEMBL
Affinity DataKi: 2.10E+3nMAssay Description:Inhibition of [3H]- RTX binding to Vanilloid receptors from pig spinal cordMore data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Institute
Curated by ChEMBL
Institute
Curated by ChEMBL
Affinity DataKi: 6.40E+3nMAssay Description:Inhibition of [3H]- RTX binding to Vanilloid receptors from human spinal cordMore data for this Ligand-Target Pair