BDBM50317180 2-[6-(beta-Carboline-2-ium-2-yl)hexyl]-beta-carboline-2-ium dibromide::CHEMBL1088355
SMILES C(CCC[n+]1ccc2c(c1)[nH]c1ccccc21)CC[n+]1ccc2c(c1)[nH]c1ccccc21
InChI Key InChIKey=MSKHZKJIIIDYDG-UHFFFAOYSA-P
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 50317180
Affinity DataIC50: 186nMAssay Description:Inhibition of equine serum BChE by modified Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 248nMAssay Description:Inhibition of electric eel AChE by modified Ellman's methodMore data for this Ligand-Target Pair
TargetGlutamate receptor ionotropic, NMDA 1/2A(Human)
Friedrich-Schiller-Universitat Jena
Curated by ChEMBL
Friedrich-Schiller-Universitat Jena
Curated by ChEMBL
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of dexamethasone-induced human NR1-1a/NR2A receptor-mediated excitotoxicity in (S)-glutamate/glycine-stimulated mouse L12-G10 cells assess...More data for this Ligand-Target Pair
TargetGlutamate receptor ionotropic, NMDA 1/2B(Human)
Friedrich-Schiller-Universitat Jena
Curated by ChEMBL
Friedrich-Schiller-Universitat Jena
Curated by ChEMBL
Affinity DataIC50: 6.50E+3nMAssay Description:Inhibition of dexamethasone-induced human NR1-1a/NR2B receptor-mediated excitotoxicity in (S)-glutamate/glycine-stimulated mouse L13-E6 cells assesse...More data for this Ligand-Target Pair
TargetGlutamate receptor ionotropic, NMDA 1/2B(Human)
Friedrich-Schiller-Universitat Jena
Curated by ChEMBL
Friedrich-Schiller-Universitat Jena
Curated by ChEMBL
Affinity DataKi: 2.00E+4nMAssay Description:Displacement of [3H]ifenprodil from human NR1-1a/NR2B receptor expressed in mouse L13-E6 cellsMore data for this Ligand-Target Pair
