null

SMILES CC(C)N1CCC(CC1)Oc1ccc2n3CCN(Cc4ccccn4)C(=O)c3cc2c1

InChI Key InChIKey=YKMUZVIXBRZDHR-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50327488   

TargetHistamine H3 receptor(Homo sapiens (Human))
F Hoffmann-La Roche Ltd

Curated by ChEMBL
LigandPNGBDBM50327488(8-(1-isopropylpiperidin-4-yloxy)-2-(pyridin-2-ylme...)copy SMILEScopy InChI
Affinity DataKi:  6nMAssay Description:Displacement of [3H]-RAMH from human histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571C7NPubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
F Hoffmann-La Roche Ltd

Curated by ChEMBL
LigandPNGBDBM50327488(8-(1-isopropylpiperidin-4-yloxy)-2-(pyridin-2-ylme...)copy SMILEScopy InChI
Affinity DataEC50:  14nMAssay Description:Inverse agonist activity at human recombinant histamine H3 receptor assessed as effect on [35S]GTPgammaS bindingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2571C7NPubMed