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BDBM50379614 CHEMBL2013048

SMILES: C1CC(C1)N1CCC2(CC1)CCc1cc(OC3CCNCC3)ccc1O2

InChI Key: InChIKey=IALVKGMYVHTORI-UHFFFAOYSA-N

Data: 2 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50379614   
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


(Homo sapiens (Human))
BDBM50379614
PNG
(CHEMBL2013048)
Show SMILES C1CC(C1)N1CCC2(CC1)CCc1cc(OC3CCNCC3)ccc1O2
Show InChI InChI=1S/C22H32N2O2/c1-2-18(3-1)24-14-10-22(11-15-24)9-6-17-16-20(4-5-21(17)26-22)25-19-7-12-23-13-8-19/h4-5,16,18-19,23H,1-3,6-15H2
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KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

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



Cephalon, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]-N-alpha-methylhistamine from human cloned histamine H3 receptor expressed in CHO cells


Bioorg Med Chem Lett 22: 2151-3 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.139
BindingDB Entry DOI: 10.7270/Q2736RX9
More data for this
Ligand-Target Pair
Histamine H3 receptor


(Rattus norvegicus (rat))
BDBM50379614
PNG
(CHEMBL2013048)
Show SMILES C1CC(C1)N1CCC2(CC1)CCc1cc(OC3CCNCC3)ccc1O2
Show InChI InChI=1S/C22H32N2O2/c1-2-18(3-1)24-14-10-22(11-15-24)9-6-17-16-20(4-5-21(17)26-22)25-19-7-12-23-13-8-19/h4-5,16,18-19,23H,1-3,6-15H2
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
6n/an/an/an/an/an/an/an/a



Cephalon, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]N-alpha-methylhistamine from rat cloned histamine H3 receptor expressed in CHO cells


Bioorg Med Chem Lett 22: 2151-3 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.139
BindingDB Entry DOI: 10.7270/Q2736RX9
More data for this
Ligand-Target Pair