Affinity DataKi: 0.260nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.350nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.660nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.730nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.75nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.880nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 3.5nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 5.5nMAssay Description:Displacement of [125I]DOI from rat 5HT2C receptorMore data for this Ligand-Target Pair
Affinity DataKi: 15nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 42nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 47nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 53nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 60nMAssay Description:Displacement of [125I]DOI from rat 5HT2C receptorMore data for this Ligand-Target Pair
Affinity DataKi: 69nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 74nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 130nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 170nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 170nMAssay Description:Displacement of (+/-)-[125I]DOI from rat cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Displacement of (+/-)-[125I]DOI from human cloned 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 360nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 380nMAssay Description:Displacement of [125I]DOI from rat 5HT2C receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.12E+3nMAssay Description:Displacement of [125I]DOI from rat 5HT2A receptorMore data for this Ligand-Target Pair
Affinity DataIC50: 2.5nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Affinity DataIC50: 13nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 32nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 40nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 40nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 50nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 63nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 70nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
Affinity DataIC50: 79nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 80nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
Affinity DataIC50: 100nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 100nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Affinity DataIC50: 126nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
Affinity DataIC50: 158nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 200nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 200nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 200nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
Affinity DataIC50: 200nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 251nMAssay Description:Immunomodulatory activity at human S1PR1 expressed in CHO-K1 EDG1 beta-arrestin cells assessed as stimulation of beta-arrestin recruitment incubated ...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 300nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 300nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 300nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair
Affinity DataIC50: 316nMAssay Description:Inhibition of S1PR1 (unknown origin) expressed in CHOK1 cells after 90 mins by beta-arresting recuitment assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Rattus norvegicus (rat))
Universidad De Chile
Curated by ChEMBL
Universidad De Chile
Curated by ChEMBL
Affinity DataIC50: 400nMAssay Description:Inhibitory concentration against monoamine oxidase A in rat brain mitochondrial suspensionMore data for this Ligand-Target Pair