BDBM50311776 (R)-3-(1H-imidazol-4-yl)propyl heptan-2-ylcarbamate::CHEMBL1079918

SMILES CCCCC[C@@H](C)NC(=O)OCCCc1cnc[nH]1

InChI Key InChIKey=JDUPATOWYGPGEY-GFCCVEGCSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50311776   

TargetHistamine H3 receptor(Rattus norvegicus (rat))
Jagiellonian University Medical College

Curated by ChEMBL
LigandPNGBDBM50311776((R)-3-(1H-imidazol-4-yl)propyl heptan-2-ylcarbamat...)
Affinity DataKi:  23nMAssay Description:Displacement of [3H]histamine from histamine H3 receptor in rat cerebral cortexMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Jagiellonian University Medical College

Curated by ChEMBL
LigandPNGBDBM50311776((R)-3-(1H-imidazol-4-yl)propyl heptan-2-ylcarbamat...)
Affinity DataKi:  41nMAssay Description:Displacement of [3H]iodoproxyfan from human histamine H3 receptor expressed in CHO-K1 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H4 receptor(Homo sapiens (Human))
Jagiellonian University Medical College

Curated by ChEMBL
LigandPNGBDBM50311776((R)-3-(1H-imidazol-4-yl)propyl heptan-2-ylcarbamat...)
Affinity DataKi:  636nMAssay Description:Displacement of [3H]histamine from human histamine H4 receptor expressed in SF9 cells coexpressing Galphai2, Gbeta1gamma2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed