BDBM50220396 CHEMBL62527

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

InChI Key InChIKey=UVFIYINSVIEJKT-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 = 50220396   

TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50220396(CHEMBL62527)
Affinity DataKi:  4.5nMAssay 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
LigandPNGBDBM50220396(CHEMBL62527)
Affinity DataKi:  3.98E+3nMAssay 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
LigandPNGBDBM50220396(CHEMBL62527)
Affinity DataKi:  2.95E+4nMAssay 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