BDBM50217096 CHEMBL105267

SMILES N[C@@H]1CCN(CCCOc2ccc(cc2)-c2ccc(cc2)C#N)C1

InChI Key InChIKey=RRBSCZCNYAJFEJ-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 = 50217096   

TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217096(CHEMBL105267)
Affinity DataKi:  6.20nMAssay Description:Binding affinity at human cloned Histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/7/2018
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217096(CHEMBL105267)
Affinity DataKi:  63nMAssay Description:Binding affinity at rat cortical Histamine 3 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
LigandPNGBDBM50217096(CHEMBL105267)
Affinity DataKi:  7.41E+3nMAssay Description:Binding affinity at human cortical Histamine 2 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
LigandPNGBDBM50217096(CHEMBL105267)
Affinity DataKi:  1.38E+4nMAssay Description:Binding affinity at human cortical Histamine 1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/7/2018
Entry Details Article
PubMed