BDBM50412453 CHEMBL458507

SMILES CCCN(CCC)C(=O)Cc1ccc(cc1)-c1ccc(CN2CCCCC2)cc1

InChI Key InChIKey=ALMYDBLKQQSJKZ-UHFFFAOYSA-N

Data  2 KI  1 IC50

  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 = 50412453   

TargetHistamine H3 receptor(Human)
University of Parma

Curated by ChEMBL
LigandPNGBDBM50412453(CHEMBL458507)
Affinity DataKi:  8.51nMAssay Description:Displacement of [3H]RAMHA from human histamine H3 receptor expressed in SK-N-MC cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/21/2013
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University of Parma

Curated by ChEMBL
LigandPNGBDBM50412453(CHEMBL458507)
Affinity DataKi:  53.7nMAssay Description:Displacement of [3H]RAMHA from histamine H3 receptor in Wistar rat brain membraneMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/21/2013
Entry Details Article
PubMed
TargetAcetylcholinesterase(Rat)
University of Parma

Curated by ChEMBL
LigandPNGBDBM50412453(CHEMBL458507)
Affinity DataIC50: 1.12E+4nMAssay Description:Inhibition of acetylcholinesterase in Wistar rat brain homogenate by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/21/2013
Entry Details Article
PubMed