BDBM50220413 CHEMBL305313

SMILES [#6]-[#6]-[#8]-[#6](=O)-[#7]-1-[#6]-[#6]-[#7](-[#6]-[#6]-[#6]-[#8]-c2ccc(cc2)-[#6](=O)\[#6]=[#6](\[#6])-[#6])-[#6]-[#6]-1

InChI Key InChIKey=GRHYGQREXSSVKK-UHFFFAOYSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50220413   

TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50220413(CHEMBL305313)
Affinity DataKi:  39nMAssay 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
LigandPNGBDBM50220413(CHEMBL305313)
Affinity DataKi:  355nMAssay 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
LigandPNGBDBM50220413(CHEMBL305313)
Affinity DataKi:  2.19E+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