BDBM50003634 1-(4,4-Diphenyl-but-3-enyl)-piperidine-3-carboxylic acid::1-(4,4-diphenylbut-3-enyl)piperidine-3-carboxylic acid::CHEMBL38686
SMILES [#8]-[#6](=O)-[#6]-1-[#6]-[#6]-[#6]-[#7](-[#6]-[#6]\[#6]=[#6](\c2ccccc2)-c2ccccc2)-[#6]-1
InChI Key InChIKey=TXQKSMSLZVKQBI-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 9 hits for monomerid = 50003634
TargetSodium- and chloride-dependent GABA transporter 1(Rat)
Ludwig-Maximilians-Universit£T M£Nchen
Curated by ChEMBL
Ludwig-Maximilians-Universit£T M£Nchen
Curated by ChEMBL
Affinity DataKi: 186nMAssay Description:Displacement of NO 711 from mouse GAT1 expressed in HEK293 cell membranes after 40 mins by LC-ESI-MS-MS-based MS binding assayMore data for this Ligand-Target Pair
Affinity DataIC50: 130nMAssay Description:Compound was tested for its ability to inhibit uptake of [3H]- GABA by cloned human GAT-1 transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 9.44E+5nMAssay Description:Compound was tested for its ability to inhibit uptake of [3H]- GABA by cloned human GAT-3 transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 5.50E+5nMAssay Description:Compound was tested for its ability to inhibit uptake of [3H]- GABA by cloned rat GAT-2 transporteMore data for this Ligand-Target Pair
Affinity DataIC50: 130nMAssay Description:Inhibition of human GAT1 expressed in COS cells assessed as decrease in [3H]GABA uptake after 10 mins by scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 200nMAssay Description:Binding affinity to GAT1More data for this Ligand-Target Pair
TargetSodium- and chloride-dependent GABA transporter 1(Mouse)
Ludwig Maximilians University At Munich
Curated by ChEMBL
Ludwig Maximilians University At Munich
Curated by ChEMBL
Affinity DataIC50: 130nMAssay Description:Inhibition of [3H]GABA uptake at mouse GAT1 expressed in HEK293 cells after 25 mins by scintillation counting analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 330nMAssay Description:In vitro inhibition of [3H]GABA uptake in rat synaptosomes was determinedMore data for this Ligand-Target Pair
Affinity DataIC50: 7.21E+6nMAssay Description:Compound was tested for its ability to inhibit uptake of [3H]- GABA by cloned human BGT-1 transporterMore data for this Ligand-Target Pair