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SMILES: O=C(CCN1CCC(Cc2cnc[nH]2)CC1)NC1CCCCC1

InChI Key: InChIKey=NBIJVGRCJJYORZ-UHFFFAOYSA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50175829   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kcal/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Histamine H3 receptor


(GUINEA PIG)
BDBM50175829
PNG
(3-(4-((1H-imidazol-4-yl)methyl)piperidin-1-yl)-N-c...)
Show SMILES O=C(CCN1CCC(Cc2cnc[nH]2)CC1)NC1CCCCC1
Show InChI InChI=1S/C18H30N4O/c23-18(21-16-4-2-1-3-5-16)8-11-22-9-6-15(7-10-22)12-17-13-19-14-20-17/h13-16H,1-12H2,(H,19,20)(H,21,23)
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
3n/an/an/an/an/an/an/an/a



The Schering Plough Research Institute

Curated by ChEMBL


Assay Description
Displacement of [3H]-N-alpha-methylhistamine from histamine H3 receptor in guinea pig brain


Bioorg Med Chem Lett 16: 395-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.076
BindingDB Entry DOI: 10.7270/Q29S1QK1
More data for this
Ligand-Target Pair
Histamine H3 receptor


(GUINEA PIG)
BDBM50175829
PNG
(3-(4-((1H-imidazol-4-yl)methyl)piperidin-1-yl)-N-c...)
Show SMILES O=C(CCN1CCC(Cc2cnc[nH]2)CC1)NC1CCCCC1
Show InChI InChI=1S/C18H30N4O/c23-18(21-16-4-2-1-3-5-16)8-11-22-9-6-15(7-10-22)12-17-13-19-14-20-17/h13-16H,1-12H2,(H,19,20)(H,21,23)
UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/a 6.31n/an/an/an/an/a



The Schering Plough Research Institute

Curated by ChEMBL


Assay Description
Antagonist potency against histamine H3 receptor in an electrically stimulated guinea pig ileum


Bioorg Med Chem Lett 16: 395-9 (2005)


Article DOI: 10.1016/j.bmcl.2005.09.076
BindingDB Entry DOI: 10.7270/Q29S1QK1
More data for this
Ligand-Target Pair