BDBM50412469 CHEMBL459756

SMILES C(Cc1ccc(cc1)-c1ccc(CN2CCCCC2)cc1)N1CCCCC1

InChI Key InChIKey=IPENPJGNQLBYMT-UHFFFAOYSA-N

Data  3 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 4 hits for monomerid = 50412469   

TargetAcetylcholinesterase(Rat)
University of Parma

Curated by ChEMBL
LigandPNGBDBM50412469(CHEMBL459756)
Affinity DataIC50: 1.10E+3nMAssay 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
TargetHistamine H3 receptor(Human)
University of Parma

Curated by ChEMBL
LigandPNGBDBM50412469(CHEMBL459756)
Affinity DataKi:  2nMAssay 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(Human)
University of Parma

Curated by ChEMBL
LigandPNGBDBM50412469(CHEMBL459756)
Affinity DataKi:  2nMAssay Description:Binding affinity to histamine H3 receptor (unknown origin)More data for this Ligand-Target Pair
In Depth
Date in BDB:
9/1/2020
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University of Parma

Curated by ChEMBL
LigandPNGBDBM50412469(CHEMBL459756)
Affinity DataKi:  8.32nMAssay 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