null

SMILES CC1CCN(Cc2ccc(cc2)-c2ccc(CN3CCCCC3)cc2)CC1

InChI Key InChIKey=DTQQVJLJZAQLBK-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50412464   

TargetHistamine H3 receptor(Homo sapiens (Human))
Universit£ degli Studi di Parma

Curated by ChEMBL
LigandPNGBDBM50412464(CHEMBL458082)copy SMILEScopy InChI
Affinity DataKi:  2.40nMAssay Description:Displacement of [3H]RAMHA from human histamine H3 receptor expressed in SK-N-MC cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FQ9XVPPubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Universit£ degli Studi di Parma

Curated by ChEMBL
LigandPNGBDBM50412464(CHEMBL458082)copy SMILEScopy InChI
Affinity DataKi:  5.75nMAssay Description:Displacement of [3H]RAMHA from histamine H3 receptor in Wistar rat brain membraneMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FQ9XVPPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Universit£ degli Studi di Parma

Curated by ChEMBL
LigandPNGBDBM50412464(CHEMBL458082)copy SMILEScopy InChI
Affinity DataIC50: 1.41E+3nMAssay Description:Inhibition of acetylcholinesterase in Wistar rat brain homogenate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FQ9XVPPubMed