BDBM50217099 CHEMBL106483

SMILES N#Cc1ccc(cc1)-c1ccc(OCCCN2CCOCC2)cc1

InChI Key InChIKey=PFEJJOZKVMFZED-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 50217099   

TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217099(CHEMBL106483)
Affinity DataKi:  25nMAssay Description:Binding affinity at rat cortical Histamine H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/7/2018
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217099(CHEMBL106483)
Affinity DataKi:  36nMAssay Description:Binding affinity at human cloned Histamine H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/7/2018
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217099(CHEMBL106483)
Affinity DataKi:  3.24E+3nMAssay Description:Binding affinity of human cortical histamine H1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/7/2018
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217099(CHEMBL106483)
Affinity DataKi:  3.80E+4nMAssay Description:Binding affinity to the human cortical histamine H2 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/7/2018
Entry Details Article
PubMed