Report error Found 58 with Last Name = 'anglada' and Initial = 'l'
Affinity DataKi: 0.700nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 2A receptor by the inhibition of [3H]-ketanserin binding to rat cortex using unlabeled mianserin...More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Human)
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Affinity DataKi: 1.5nMAssay Description:Binding affinity measured at the sigma receptor by the inhibition of [3H]-3-PPP binding to guinea pig cerebellum using unlabeled 3-PPP for nonspecifi...More data for this Ligand-Target Pair
Affinity DataKi: 1.90nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 2A receptor by the inhibition of [3H]-ketanserin binding to rat cortex using unlabeled mianserin...More data for this Ligand-Target Pair
Affinity DataKi: 2.40nMAssay Description:Binding affinity measured at the Alpha-1A adrenergic receptor by the inhibition of [3H]-prazosin binding to rat cortex using unlabeled WB-4101 for no...More data for this Ligand-Target Pair
Affinity DataKi: 4.30nMAssay Description:Binding affinity measured at the Dopamine receptor D4 by the inhibition of [3H]-spiperone binding to human recombinant CHO cells using unlabeled halo...More data for this Ligand-Target Pair
Affinity DataKi: 5.40nMAssay Description:Binding affinity measured at the Dopamine receptor D3 by the inhibition of [3H]-YM-09151-2 binding to human recombinant CCL 1.3 cells using unlabeled...More data for this Ligand-Target Pair
Affinity DataKi: 6.20nMAssay Description:Binding affinity measured at the Dopamine receptor D4 by the inhibition of [3H]-spiperone binding to human recombinant CHO cells using unlabeled halo...More data for this Ligand-Target Pair
Affinity DataKi: 9.40nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 2A receptor by the inhibition of [3H]-ketanserin binding to rat cortex using unlabeled mianserin...More data for this Ligand-Target Pair
Affinity DataKi: 9.80nMAssay Description:Binding affinity measured at the Dopamine receptor D2 by the inhibition of [3H]-methylspiperone binding to rat striatum using unlabeled haloperidol f...More data for this Ligand-Target Pair
Affinity DataKi: 12nMAssay Description:Binding affinity measured at the Dopamine receptor D2 by the inhibition of [3H]-methylspiperone binding to rat striatum using unlabeled haloperidol f...More data for this Ligand-Target Pair
Affinity DataKi: 13nMAssay Description:Binding affinity measured at the Alpha-1A adrenergic receptor by the inhibition of [3H]-prazosin binding to rat cortex using unlabeled WB-4101 for no...More data for this Ligand-Target Pair
TargetAlpha-2A adrenergic receptor [16-465](Rat)
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Affinity DataKi: 19nMAssay Description:Binding affinity measured at the Alpha-2 adrenergic receptor by the inhibition of [3H]-clonidine binding to rat cortex using unlabeled NAbitartrate f...More data for this Ligand-Target Pair
Affinity DataKi: 19nMAssay Description:Binding affinity measured at the Dopamine receptor D2 by the inhibition of [3H]-methylspiperone binding to rat striatum using unlabeled haloperidol f...More data for this Ligand-Target Pair
Affinity DataKi: 22nMAssay Description:Binding affinity measured at the Alpha-1A adrenergic receptor by the inhibition of [3H]-prazosin binding to rat cortex using unlabeled WB-4101 for no...More data for this Ligand-Target Pair
TargetAlpha-2A adrenergic receptor [16-465](Rat)
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Affinity DataKi: 25nMAssay Description:Binding affinity measured at the Alpha-2 adrenergic receptor by the inhibition of [3H]-clonidine binding to rat cortex using unlabeled NAbitartrate f...More data for this Ligand-Target Pair
Affinity DataKi: 31nMAssay Description:Binding affinity measured at the Dopamine receptor D3 by the inhibition of [3H]-YM-09151-2 binding to human recombinant CCL 1.3 cells using unlabeled...More data for this Ligand-Target Pair
Affinity DataKi: 36nMAssay Description:Binding affinity measured at the Dopamine receptor D4 by the inhibition of [3H]-spiperone binding to human recombinant CHO cells using unlabeled halo...More data for this Ligand-Target Pair
Affinity DataKi: 75nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 2A receptor by the inhibition of [3H]-ketanserin binding to rat cortex using unlabeled mianserin...More data for this Ligand-Target Pair
Affinity DataKi: 93nMAssay Description:Binding affinity measured at the Dopamine receptor D2 by the inhibition of [3H]-methylspiperone binding to rat striatum using unlabeled haloperidol f...More data for this Ligand-Target Pair
Affinity DataKi: 94nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 1A receptor by the inhibition of [3H]-8-OH-DPAT binding to rat cortex using unlabeled buspirone ...More data for this Ligand-Target Pair
Affinity DataKi: 145nMAssay Description:Binding affinity measured at the Dopamine receptor D1 by the inhibition of [3H]-SCH-23,390 binding to rat striatum using unlabeled apomorphine for no...More data for this Ligand-Target Pair
Affinity DataKi: 179nMAssay Description:Binding affinity measured at the Dopamine receptor D4 by the inhibition of [3H]-spiperone binding to human recombinant CHO cells using unlabeled halo...More data for this Ligand-Target Pair
Affinity DataKi: 235nMAssay Description:Binding affinity measured at the Dopamine receptor D1 by the inhibition of [3H]-SCH-23,390 binding to rat striatum using unlabeled apomorphine for no...More data for this Ligand-Target Pair
Affinity DataKi: 239nMAssay Description:Binding affinity measured at the Dopamine receptor D1 by the inhibition of [3H]-SCH-23,390 binding to rat striatum using unlabeled apomorphine for no...More data for this Ligand-Target Pair
Affinity DataKi: 247nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 1A receptor by the inhibition of [3H]-8-OH-DPAT binding to rat cortex using unlabeled buspirone ...More data for this Ligand-Target Pair
Affinity DataKi: 251nMAssay Description:Binding affinity measured at the Dopamine receptor D1 by the inhibition of [3H]-SCH-23,390 binding to rat striatum using unlabeled apomorphine for no...More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Human)
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Affinity DataKi: 490nMAssay Description:Binding affinity measured at the sigma receptor by the inhibition of [3H]-3-PPP binding to guinea pig cerebellum using unlabeled 3-PPP for nonspecifi...More data for this Ligand-Target Pair
Affinity DataKi: 491nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 1A receptor by the inhibition of [3H]-8-OH-DPAT binding to rat cortex using unlabeled buspirone ...More data for this Ligand-Target Pair
Affinity DataKi: 513nMAssay Description:Binding affinity measured at the Dopamine receptor D3 by the inhibition of [3H]-YM-09151-2 binding to human recombinant CCL 1.3 cells using unlabeled...More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Human)
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Affinity DataKi: 4.30E+3nMAssay Description:Binding affinity measured at the sigma receptor by the inhibition of [3H]-3-PPP binding to guinea pig cerebellum using unlabeled 3-PPP for nonspecifi...More data for this Ligand-Target Pair
Affinity DataKi: 8.40E+3nMAssay Description:Binding affinity measured at the 5-hydroxytryptamine 1A receptor by the inhibition of [3H]-8-OH-DPAT binding to rat cortex using unlabeled buspirone ...More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Human)
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Centro De InvestigacióN Grupo Ferrer
Curated by ChEMBL
Affinity DataKi: 8.50E+3nMAssay Description:Binding affinity measured at the sigma receptor by the inhibition of [3H]-3-PPP binding to guinea pig cerebellum using unlabeled 3-PPP for nonspecifi...More data for this Ligand-Target Pair
Affinity DataKi: 2.20E+4nMAssay Description:Binding affinity measured at the Beta-1 adrenergic receptor by the inhibition of [3H]-DHA binding to rat cortex using unlabeled isoprenalin for nonsp...More data for this Ligand-Target Pair
Affinity DataKi: 2.60E+4nMAssay Description:Binding affinity measured at the Beta-1 adrenergic receptor by the inhibition of [3H]-DHA binding to rat cortex using unlabeled isoprenalin for nonsp...More data for this Ligand-Target Pair
Affinity DataIC50: 0.600nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 2.10nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 6.20nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 7.20nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 8.60nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 11.3nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 12.8nMAssay Description:Inhibition of [3H]-methylspiperone binding to rat striatal membrane Dopamine receptor D2More data for this Ligand-Target Pair
Affinity DataIC50: 13nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 13.1nMAssay Description:Inhibition of [3H]-methylspiperone binding to rat striatal membrane Dopamine receptor D2More data for this Ligand-Target Pair
Affinity DataIC50: 13.7nMAssay Description:Inhibition of [3H]-methylspiperone binding to rat striatal membrane Dopamine receptor D2More data for this Ligand-Target Pair
Affinity DataIC50: 16.6nMAssay Description:Inhibition of [3H]-methylspiperone binding to rat striatal membrane Dopamine receptor D2More data for this Ligand-Target Pair
Affinity DataIC50: 17nMAssay Description:Inhibition of [3H]-methylspiperone binding to rat striatal membrane Dopamine receptor D2More data for this Ligand-Target Pair
Affinity DataIC50: 25.3nMAssay Description:Inhibition of [3H]-ketanserin binding to rat frontal cortex membrane 5-hydroxytryptamine 2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 27nMAssay Description:Inhibition of [3H]-methylspiperone binding to rat striatal membrane Dopamine receptor D2More data for this Ligand-Target Pair