BDBM50217418 CHEMBL421026

SMILES N#Cc1ccc(cc1)-c1ccc(OCCCN2CC3CNCC3C2)cc1

InChI Key InChIKey=IVRXDSYEBGHJBD-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 = 50217418   

TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217418(CHEMBL421026)
Affinity DataKi:  15nMAssay 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 H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217418(CHEMBL421026)
Affinity DataKi:  66nMAssay 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 H1 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50217418(CHEMBL421026)
Affinity DataKi:  2.88E+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
LigandPNGBDBM50217418(CHEMBL421026)
Affinity DataKi:  1.23E+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