BDBM50067472 4-[3-(4-Ethynyl-phenoxy)-propyl]-1H-imidazole::4-[3-(4-Ethynyl-phenoxy)-propyl]-1H-imidazole (FUB 470)::CHEMBL309600

SMILES C#Cc1ccc(OCCCc2cnc[nH]2)cc1

InChI Key InChIKey=LMKPPWNWUJXSAQ-UHFFFAOYSA-N

Data  3 KI

  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 3 hits for monomerid = 50067472   

TargetHistamine H3 receptor(Rattus norvegicus (rat))
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50067472(4-[3-(4-Ethynyl-phenoxy)-propyl]-1H-imidazole | 4-...)
Affinity DataKi:  2.30nMAssay Description:In vitro antagonist potency at Histamine H3 receptor measured as K+-evoked [3H]-histamine release from synaptosomes of rat cerebral cortex.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50067472(4-[3-(4-Ethynyl-phenoxy)-propyl]-1H-imidazole | 4-...)
Affinity DataKi:  2.30nMAssay Description:Effect on histamine H3 receptors in vitro, on synaptosomes of rat cerebral cortex for the release of [3H]histamineMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Freie UniversitäT Berlin

Curated by ChEMBL
LigandPNGBDBM50067472(4-[3-(4-Ethynyl-phenoxy)-propyl]-1H-imidazole | 4-...)
Affinity DataKi:  2.30nMAssay Description:In vitro inhibitory activity against Histamine H3 receptor for K+ evoked depolarization-induced release of [3H]-histamine from synaptosomes of rat ce...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed