BDBM50217414 CHEMBL102416

SMILES OC1CCN(CCCOc2ccc(cc2)-c2ccc(cc2)C#N)CC1

InChI Key InChIKey=CRGOWMIZBWIMTB-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 = 50217414   

TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217414(CHEMBL102416)
Affinity DataKi:  32nMAssay 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
LigandPNGBDBM50217414(CHEMBL102416)
Affinity DataKi:  123nMAssay 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
LigandPNGBDBM50217414(CHEMBL102416)
Affinity DataKi:  575nMAssay 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
LigandPNGBDBM50217414(CHEMBL102416)
Affinity DataKi:  1.00E+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