BDBM50139392 CHEMBL422360::Morpholin-4-yl-{6-[2-(2-pyrrolidin-1-yl-ethyl)-benzofuran-5-yl]-pyridin-3-yl}-methanone

SMILES O=C(N1CCOCC1)c1ccc(nc1)-c1ccc2oc(CCN3CCCC3)cc2c1

InChI Key InChIKey=RRLCACGGDHPKNQ-UHFFFAOYSA-N

Data  4 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 4 hits for monomerid = 50139392   

TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50139392(CHEMBL422360 | Morpholin-4-yl-{6-[2-(2-pyrrolidin-...)
Affinity DataKi:  3.90nMAssay Description:Binding potency was determined by displacement of [3H]-N-alpha-methyl histamine from cloned human histamine H3 receptor expressed in C6 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50139392(CHEMBL422360 | Morpholin-4-yl-{6-[2-(2-pyrrolidin-...)
Affinity DataKi:  4nMAssay Description:Binding potency was determined by displacement of [3H]N-alpha-methyl histamine from cloned human histamine H3 receptor expressed in C6 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50139392(CHEMBL422360 | Morpholin-4-yl-{6-[2-(2-pyrrolidin-...)
Affinity DataKi:  29nMAssay Description:Binding potency was determined by displacement of [3H]-N-alpha-methyl histamine from histamine H3 receptor of rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50139392(CHEMBL422360 | Morpholin-4-yl-{6-[2-(2-pyrrolidin-...)
Affinity DataKi:  30nMAssay Description:Binding potency was determined by displacement of [3H]N-alpha-methyl histamine from histamine H3 receptor of rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed