BDBM54832 3-methyl-N-[9-(phenylmethyl)-9-azabicyclo[3.3.1]nonan-3-yl]benzamide::MLS001212730::N-(9-Benzyl-9-aza-bicyclo[3.3.1]non-3-yl)-3-methyl-benzamide::N-(9-benzyl-9-azabicyclo[3.3.1]nonan-3-yl)-3-methyl-benzamide::N-(9-benzyl-9-azabicyclo[3.3.1]nonan-3-yl)-3-methylbenzamide::SMR000503762::cid_3218091
SMILES [H]C12CCCC([H])(CC(C1)NC(=O)c1cccc(C)c1)N2Cc1ccccc1
InChI Key InChIKey=XPZSKTMTRDBTQE-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 54832
TargetKappa-type opioid receptor(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.99E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Broad Institute
Curated by PubChem BioAssay
Broad Institute
Curated by PubChem BioAssay
Affinity DataEC50: >3.00E+5nMAssay Description:Keywords: GSK3beta, dose response, kinase, inhibition, HTS Assay Overview: The glycogen synthase kinase-3 beta (GSK-3b) is a known master regulator f...More data for this Ligand-Target Pair
TargetKappa-type opioid receptor(Homo sapiens (Human))
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Burnham Center For Chemical Genomics
Curated by PubChem BioAssay
Affinity DataIC50: 1.57E+4nMAssay Description:Data Source: Sanford-Burnham Center for Chemical Genomics (SBCCG) Source Affiliation: Sanford-Burnham Medical Research Institute (SBMRI, San Diego, C...More data for this Ligand-Target Pair