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Binding affinity towards human HRH3 in an in vitro assay with cellular components measured by scintillation counting
Assay data:41 Active, 7 Activity ≤ 1 µM, 993 Tested
SummaryRelated BioAssays by Target
Antagonist activity at human ADRA1A in an in vitro cell-based assay measured by fluorescence spectroscopy
Assay data:117 Active, 53 Activity ≤ 1 µM, 881 Tested
Binding affinity towards human DRD3 in an in vitro assay with cellular components measured by scintillation counting
Assay data:176 Active, 1 Activity ≤ 1 nM, 87 Activity ≤ 1 µM, 1215 Tested
Compound was evaluated for inhibition of human PDE3A in an in vitro cell free assay measured by time-resolved fluorescence resonance energy transfer method
Assay data:49 Active, 5 Activity ≤ 1 µM, 1243 Tested
Compound was evaluated for inhibition of human MAOA in an in vitro cell free assay measured by fluorescence spectroscopy
Assay data:28 Active, 4 Activity ≤ 1 µM, 1218 Tested
Binding affinity towards human OPRM1 in an in vitro assay with cellular components measured by scintillation counting
Assay data:60 Active, 9 Activity ≤ 1 µM, 766 Tested
Binding affinity towards human SLC6A4 in an in vitro assay with cellular components measured by scintillation counting
Assay data:148 Active, 75 Activity ≤ 1 µM, 1194 Tested
Binding affinity towards human SLC6A2 in an in vitro assay with cellular components measured by scintillation counting
Assay data:123 Active, 40 Activity ≤ 1 µM, 1197 Tested
Binding affinity towards human SLC6A3 in an in vitro assay with cellular components measured by scintillation counting
Assay data:119 Active, 21 Activity ≤ 1 µM, 1213 Tested
Binding affinity towards human TBXA2R in an in vitro assay with cellular components measured by scintillation proximity assay
Assay data:14 Active, 2 Activity ≤ 1 µM, 1022 Tested
Agonist activity at human TBXA2R in an in vitro cell-based assay (CRO assay) measured by fluorescence spectroscopy
Assay data:13 Active, 8 Activity ≤ 1 µM, 927 Tested
Assay data:99 Active, 36 Activity ≤ 1 µM, 927 Tested
Assay data:128 Active, 38 Activity ≤ 1 µM, 927 Tested
Assay data:137 Active, 27 Activity ≤ 1 µM, 927 Tested
Binding affinity towards human SLC29A1 in an in vitro assay with cellular components measured by scintillation proximity assay
Assay data:20 Active, 4 Activity ≤ 1 µM, 1115 Tested
Antagonist activity at human RARG in an in vitro cell-based assay measured by time-resolved fluorescence resonance energy transfer method
Assay data:5 Active, 36 Tested
Agonist activity at human RARG in an in vitro cell-based assay measured by time-resolved fluorescence resonance energy transfer method
Assay data:1 Active, 38 Tested
Antagonist activity at human RARB in an in vitro cell-based assay measured by time-resolved fluorescence resonance energy transfer method
Assay data:3 Active, 36 Tested
Agonist activity at human RARB in an in vitro cell-based assay measured by time-resolved fluorescence resonance energy transfer method
Antagonist activity at human RARA in an in vitro cell-based assay measured by time-resolved fluorescence resonance energy transfer method
Assay data:36 Tested
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