BDBM50220111 CHEMBL64334

SMILES CCCCCC(=O)c1ccc(OCCCN2CCN(CCCC)CC2)cc1

InChI Key InChIKey=CWMROIPYLYIONF-UHFFFAOYSA-N

Data  3 KI

  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 = 50220111   

TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50220111(CHEMBL64334)
Affinity DataKi:  13nMAssay Description:Binding affinity for the rat cortical Histamine H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/2/2018
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50220111(CHEMBL64334)
Affinity DataKi:  661nMAssay Description:Binding affinity for the human Histamine H1 ReceptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/2/2018
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50220111(CHEMBL64334)
Affinity DataKi:  7.59E+3nMAssay Description:Binding affinity for the human Histamine H2 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/2/2018
Entry Details Article
PubMed