Report error Found 53 Enz. Inhib. hit(s) with all data for entry = 50016851
Affinity DataIC50: 1.10nMAssay Description:Inhibition of recombinant human MAO-B assessed as measuring amount of 4-hydroxyquinoline using kynuramine as substrate incubated for 20 mins by fluor...More data for this Ligand-Target Pair
Affinity DataIC50: 1.20nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate by fluorescence spectrophotometryMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate by fluorescence spectrophotometryMore data for this Ligand-Target Pair
Affinity DataIC50: 5.90nMAssay Description:Inhibition of BuChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 6.40nMAssay Description:Inhibition of MAO-B (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 10nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate by fluorescence spectrophotometryMore data for this Ligand-Target Pair
Affinity DataIC50: 13nMAssay Description:Inhibition of MAO-B (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 32nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 36nMAssay Description:Inhibition of recombinant human MAO-A assessed as measuring amount of 4-hydroxyquinoline using kynuramine as substrate incubated for 20 mins by fluor...More data for this Ligand-Target Pair
Affinity DataIC50: 45nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 47nMAssay Description:Inhibition of recombinant bovine mitochondrial MAO-A using benzylamine or serotonin as substrate incubated for 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
Affinity DataIC50: 47nMAssay Description:Inhibition of recombinant human MAO-B using kynuramine as substrate by fluorescence spectrophotometryMore data for this Ligand-Target Pair
Affinity DataIC50: 59nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 366nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate by fluorescence spectrophotometryMore data for this Ligand-Target Pair
Affinity DataIC50: 570nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 707nMAssay Description:Inhibition of human MAO-B assessed as measuring amount of 4-hydroxyquinoline using kynuramine as substrate incubated for 20 mins by fluorescence spec...More data for this Ligand-Target Pair
Affinity DataIC50: 741nMAssay Description:Inhibition of recombinant human MAO-A using kynuramine as substrate by fluorescence spectrophotometryMore data for this Ligand-Target Pair
Affinity DataIC50: 754nMAssay Description:Inhibition of MAO-A (unknown origin)More data for this Ligand-Target Pair
Target1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial(Human)
Northwest University
Curated by ChEMBL
Northwest University
Curated by ChEMBL
Affinity DataIC50: 900nMAssay Description:Inhibition of CYP24 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 920nMAssay Description:Inhibition of recombinant bovine mitochondrial MAO-A using benzylamine or serotonin as substrate incubated for 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
Affinity DataIC50: 990nMAssay Description:Inhibition of recombinant bovine mitochondrial MAO-A using benzylamine or serotonin as substrate incubated for 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.24E+3nMAssay Description:Inhibition of recombinant bovine mitochondrial MAO-A using benzylamine or serotonin as substrate incubated for 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.37E+3nMAssay Description:Inhibition of human MAO-A assessed as measuring amount of 4-hydroxyquinoline using kynuramine as substrate incubated for 20 mins by fluorescence spec...More data for this Ligand-Target Pair
Affinity DataIC50: 1.79E+3nMAssay Description:Inhibition of MAO-A (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.96E+3nMAssay Description:Inhibition of human MAO-A assessed as measuring amount of 4-hydroxyquinoline using kynuramine as substrate incubated for 20 mins by fluorescence spec...More data for this Ligand-Target Pair
Affinity DataIC50: 2.92E+3nMAssay Description:Inhibition of AChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Target1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial(Human)
Northwest University
Curated by ChEMBL
Northwest University
Curated by ChEMBL
Affinity DataIC50: 3.50E+3nMAssay Description:Displacement of 25-hydroxy-[26,27-methyl-3H]-vitamin D3 from CYP24 in 1,25(OH)2D3-treated human DU-145 cells using 25-(OH)D3 as substrate pretreated ...More data for this Ligand-Target Pair
Affinity DataIC50: 4.34E+3nMAssay Description:Displacement of [3H]DPCPX from A1AR in rat whole brain membrane assessed as inhibition constant by radioligand competitive binding assayMore data for this Ligand-Target Pair
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of BuChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 6.50E+3nMAssay Description:Inhibition of BuChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 6.84E+3nMAssay Description:Displacement of [3H]DPCPX from A1AR in rat whole brain membrane assessed as inhibition constant by radioligand competitive binding assayMore data for this Ligand-Target Pair
Affinity DataIC50: 7.05E+3nMAssay Description:Displacement of [3H]NECA from A2AAR in rat striatal membrane assessed as inhibition constant by radioligand competitive binding assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.25E+4nMAssay Description:Inhibition of BuChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.75E+4nMAssay Description:Inhibition of BuChE (unknown origin) using acetylthiocholine iodide as substrate incubated for 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 8.28E+5nMAssay Description:Inhibition of recombinant bovine mitochondrial MAO-A using benzylamine or serotonin as substrate incubated for 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.49E+5nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine as substrate preincubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 5.69E+8nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine as substrate preincubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.08E+6nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine as substrate preincubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40E+6nMAssay Description:Inhibition of AChE (unknown origin) using acetylcholine as substrate preincubated for 15 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataKi: 1.60nMAssay Description:Binding affinity to 5-HT2A receptor (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
Affinity DataKi: 2.70nMAssay Description:Binding affinity to 5-HT2A receptor (unknown origin) assessed as inhibition constantMore data for this Ligand-Target Pair
Affinity DataKi: 1.61E+3nMAssay Description:Displacement of [3H]NECA from A2AAR in rat striata assessed as inhibition constant in presence of N6-cyclopentyladenosine by radioligand competitive ...More data for this Ligand-Target Pair
Affinity DataKi: 1.62E+3nMAssay Description:Displacement of [3H]DPCPX from A1AR in rat whole brain assessed as inhibition constant by radioligand competitive binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 1.64E+3nMAssay Description:Displacement of [3H]DPCPX from A1AR in rat whole brain assessed as inhibition constant by radioligand competitive binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 4.70E+3nMAssay Description:Displacement of isotopically-labeled PPAR-gamma (unknown origin) assessed as inhibition constant by competitive inhibition assayMore data for this Ligand-Target Pair
Affinity DataKi: 4.90E+3nMAssay Description:Displacement of isotopically-labeled PPAR-gamma (unknown origin) assessed as inhibition constant by competitive inhibition assayMore data for this Ligand-Target Pair
Affinity DataKi: 5.46E+3nMAssay Description:Displacement of [3H]NECA from A2AAR in rat striata assessed as inhibition constant in presence of N6-cyclopentyladenosine by radioligand competitive ...More data for this Ligand-Target Pair
Affinity DataKi: 5.80E+3nMAssay Description:Displacement of isotopically-labeled PPAR-gamma (unknown origin) assessed as inhibition constant by competitive inhibition assayMore data for this Ligand-Target Pair
Affinity DataKi: 9.92E+3nMAssay Description:Displacement of [3H]NECA from A2AAR in rat striata assessed as inhibition constant in presence of N6-cyclopentyladenosine by radioligand competitive ...More data for this Ligand-Target Pair
Affinity DataKi: 1.14E+4nMAssay Description:Displacement of [3H]DPCPX from A1AR in rat whole brain assessed as inhibition constant by radioligand competitive binding assayMore data for this Ligand-Target Pair
