Affinity DataKi: 5.20nMAssay Description:Displacement of [3H]-diprenorphine from human delta opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation c...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataKi: 7.30nMAssay Description:Competitive inhibition of recombinant human MAO-B using kynuramine as substrate pre-incubated for 15 mins followed by 2 fold compound dilution for 24...More data for this Ligand-Target Pair
Affinity DataKi: 7.30nMAssay Description:Displacement of [3H]-diprenorphine from human delta opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation c...More data for this Ligand-Target Pair
Affinity DataKi: 15nMAssay Description:Displacement of [3H]diprenorphine human delta opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 24nMAssay Description:Displacement of [3H]-diprenorphine from human kappa opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation c...More data for this Ligand-Target Pair
Affinity DataKi: 43nMAssay Description:Displacement of [3H]diprenorphine human MOR expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 51nMAssay Description:Displacement of [3H]-diprenorphine from human mu opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation coun...More data for this Ligand-Target Pair
Affinity DataKi: 54nMAssay Description:Displacement of [3H]-diprenorphine from human mu opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation coun...More data for this Ligand-Target Pair
Affinity DataKi: 70nMAssay Description:Displacement of [3H]-diprenorphine from human delta opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation c...More data for this Ligand-Target Pair
Affinity DataKi: 76nMAssay Description:Displacement of [3H]-diprenorphine from human mu opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation coun...More data for this Ligand-Target Pair
Affinity DataKi: 91nMAssay Description:Displacement of [3H]diprenorphine human MOR expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 98nMAssay Description:Displacement of [3H]diprenorphine human delta opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 120nMAssay Description:Displacement of [3H]diprenorphine human kappa opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 120nMAssay Description:Displacement of [3H]diprenorphine human delta opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 120nMAssay Description:Displacement of [3H]diprenorphine human delta opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 495nMAssay Description:Displacement of [3H]-diprenorphine from human kappa opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation c...More data for this Ligand-Target Pair
Affinity DataKi: 510nMAssay Description:Displacement of [3H]diprenorphine human MOR expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: 686nMAssay Description:Displacement of [3H]-diprenorphine from human kappa opioid receptor expressed in CHO cell membranes incubated for 1 hr by micro beta2 scintillation c...More data for this Ligand-Target Pair
Affinity DataKi: 790nMAssay Description:Displacement of [3H]diprenorphine human MOR expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: >3.33E+3nMAssay Description:Displacement of [3H]diprenorphine human kappa opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: >3.33E+3nMAssay Description:Displacement of [3H]diprenorphine human kappa opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataKi: >3.33E+3nMAssay Description:Displacement of [3H]diprenorphine human kappa opioid receptor expressed in CHO cell membranes after 1 hr by micro beta2 scintillation counting methodMore data for this Ligand-Target Pair
Affinity DataIC50: 0.360nMAssay Description:Antagonist activity at human delta opioid receptor expressed in CHO cell membranes assessed as reduction in SNC80-induced [35S]GTPgammaS binding incu...More data for this Ligand-Target Pair
Affinity DataIC50: <0.510nMAssay Description:Antagonist activity at human delta opioid receptor expressed in CHO cells assessed as reduction in SNC80-induced inhibition of forskolin stimulated c...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 4.5nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 5.30nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 7.20nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 8.60nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 12nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 20nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 45nMAssay Description:Antagonist activity at human delta opioid receptor expressed in CHO cell membranes assessed as reduction in SNC80-induced [35S]GTPgammaS binding incu...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 47nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 53nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 55nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 95nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 101nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 118nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 146nMAssay Description:Antagonist activity at human delta opioid receptor expressed in CHO cell membranes assessed as reduction in SNC80-induced [35S]GTPgammaS binding incu...More data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 182nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 189nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 237nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 351nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 355nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 626nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 716nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 1.07E+3nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 1.59E+3nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 1.82E+3nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
"G. D'Annunzio" University Of Chieti-Pescara
Curated by ChEMBL
Affinity DataIC50: 2.56E+3nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate after 20 mins by fluorescence assayMore data for this Ligand-Target Pair