BDBM50412464 CHEMBL458082

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

InChI Key InChIKey=DTQQVJLJZAQLBK-UHFFFAOYSA-N

Data  2 KI  1 IC50

  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 = 50412464   

TargetHistamine H3 receptor(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50412464(CHEMBL458082)
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 ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50412464(CHEMBL458082)
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 ArticlePubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Universit£

Curated by ChEMBL
LigandPNGBDBM50412464(CHEMBL458082)
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 ArticlePubMed