BDBM50090647 (4S,5S)-4-(3,4-Difluoro-phenyl)-5-methyl-2-oxo-oxazolidine-3-carboxylic acid {3-[4-(4-fluoro-phenyl)-piperidin-1-yl]-propyl}-amide::(4S,5S)-4-(3,4-difluorophenyl)-N-(3-(4-(4-fluorophenyl)piperidin-1-yl)propyl)-5-methyl-2-oxooxazolidine-3-carboxamide::4-(3,4-Difluoro-phenyl)-5-methyl-2-oxo-oxazolidine-3-carboxylic acid {3-[4-(4-fluoro-phenyl)-piperidin-1-yl]-propyl}-amide::CHEMBL96467::SNAP-7915
SMILES C[C@@H]1OC(=O)N([C@H]1c1ccc(F)c(F)c1)C(=O)NCCCN1CCC(CC1)c1ccc(F)cc1
InChI Key InChIKey=DTYAFBJXWWLRMA-QMHKHESXSA-N
Data 23 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 23 hits for monomerid = 50090647
Affinity DataKi: 0.170nMAssay Description:Tested for binding affinity against recombinant human Alpha-1A adrenergic receptor using [125I]HEAT in competition binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 0.170nMAssay Description:Binding constant measured against Alpha-1A adrenergic receptor in human prostate; +++:highly activeMore data for this Ligand-Target Pair
Affinity DataKi: 0.170nMAssay Description:Binding affinity of the compound towards Alpha1A human adrenergic receptors, using [125I]-HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 0.230nMAssay Description:Binding affinity towards Alpha1A dog adrenergic receptors, using [125I]HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 0.360nMAssay Description:Binding affinity towards Alpha1A rat adrenergic receptors, using [125I]HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >45nMAssay Description:Binding affinity towards human alpha-2A-adrenergic receptor, using [3H]rauwolscine as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >45nMAssay Description:Binding affinity towards human alpha-2B-adrenergic receptor, using [3H]rauwolscine as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >45nMAssay Description:Binding affinity towards human alpha-2C-adrenergic receptor, using [3H]rauwolscine as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 54nMAssay Description:Binding affinity towards Histamine H1 receptor in human brain tissue preparation, using [3H]rauwolscine as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 62nMAssay Description:Binding affinity towards Alpha1D rat adrenergic receptors, using [125I]HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 79nMAssay Description:Binding affinity towards Alpha1B rat adrenergic receptors, using [125I]HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 119nMAssay Description:Tested for binding affinity against recombinant human Alpha-1B adrenergic receptor using [125I]HEAT in competition binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 119nMAssay Description:Binding affinity of the compound towards Alpha1B human adrenergic receptors, using [125I]-HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 121nMAssay Description:Binding affinity towards Alpha1B dog adrenergic receptors, using [125I]HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 122nMAssay Description:Binding affinity towards Alpha1D human adrenergic receptors, using [125I]HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 122nMAssay Description:Tested for binding affinity against recombinant human Alpha-1D adrenergic receptor using [125I]-HEAT in competition binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 133nMAssay Description:Binding affinity of the compound towards Alpha1D dog adrenergic receptors, using [125I]-HEAT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >500nMAssay Description:Binding affinity towards 5-HT1D receptor, using [3H]5-HT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >500nMAssay Description:Binding affinity towards 5-hydroxytryptamine 2A receptor using [3H]5-HT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >500nMAssay Description:Binding affinity towards 5-hydroxytryptamine 1A receptor receptor, using [3H]5-HT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >500nMAssay Description:Binding affinity towards 5-hydroxytryptamine 1B receptor using [3H]5-HT as radioligand.More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:Binding affinity towards human Histamine H2 receptor, using [3H]tiotidine as radioligand.More data for this Ligand-Target Pair
TargetVoltage-dependent L-type calcium channel subunit alpha-1C/alpha-1D/alpha-1S(Rattus norvegicus)
Synaptic Pharmaceutical
Curated by ChEMBL
Synaptic Pharmaceutical
Curated by ChEMBL
Affinity DataKi: >1.00E+3nMAssay Description:Inhibition of [3H]nitrendipine binding to rat L-type Ca-channel receptorMore data for this Ligand-Target Pair