null

SMILES CN1[C@@H]2CCC[C@@H]1CC(C2)NC(=O)c1cccc2oc(nc12)N1CCOCC1

InChI Key InChIKey=RXDWERDONCYTQT-HZPDHXFCSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50329722   

Target5-hydroxytryptamine receptor 3A(Homo sapiens (Human))
AMRI

Curated by ChEMBL
LigandPNGBDBM50329722(CHEMBL1271519 | endo-N-((1R,5R)-9-methyl-9-azabicy...)copy SMILEScopy InChI
Affinity DataKi:  40nMAssay Description:Binding affinity to human HT3A receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZVHPubMed
TargetCytochrome P450 3A4(Homo sapiens (Human))
AMRI

Curated by ChEMBL
LigandPNGBDBM50329722(CHEMBL1271519 | endo-N-((1R,5R)-9-methyl-9-azabicy...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of human CYP3A4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZVHPubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
AMRI

Curated by ChEMBL
LigandPNGBDBM50329722(CHEMBL1271519 | endo-N-((1R,5R)-9-methyl-9-azabicy...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of human ERG expressed in HEK cells by patch clamp techniqueMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z31ZVHPubMed