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BDBM50365052 CHEMBL1951061

SMILES: C[C@@H]1CCCN1CCCOc1ccc(cc1)C(=O)C(C)(C)N1CCOCC1

InChI Key: InChIKey=BHDCLPFWVQAYDG-GOSISDBHSA-N

Data: 2 KI

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50365052   
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))
BDBM50365052
PNG
(CHEMBL1951061)
Show SMILES C[C@@H]1CCCN1CCCOc1ccc(cc1)C(=O)C(C)(C)N1CCOCC1 |r|
Show InChI InChI=1S/C22H34N2O3/c1-18-6-4-11-23(18)12-5-15-27-20-9-7-19(8-10-20)21(25)22(2,3)24-13-16-26-17-14-24/h7-10,18H,4-6,11-17H2,1-3H3/t18-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
9n/an/an/an/an/an/an/an/a



Cephalon, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]NAMH from human histamine H3 receptor


Bioorg Med Chem Lett 22: 1546-9 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.004
BindingDB Entry DOI: 10.7270/Q2C24WWN
More data for this
Ligand-Target Pair
Histamine H3 receptor


(Rattus norvegicus (rat))
BDBM50365052
PNG
(CHEMBL1951061)
Show SMILES C[C@@H]1CCCN1CCCOc1ccc(cc1)C(=O)C(C)(C)N1CCOCC1 |r|
Show InChI InChI=1S/C22H34N2O3/c1-18-6-4-11-23(18)12-5-15-27-20-9-7-19(8-10-20)21(25)22(2,3)24-13-16-26-17-14-24/h7-10,18H,4-6,11-17H2,1-3H3/t18-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
33n/an/an/an/an/an/an/an/a



Cephalon, Inc.

Curated by ChEMBL


Assay Description
Displacement of [3H]NAMH from rat histamine H3 receptor


Bioorg Med Chem Lett 22: 1546-9 (2012)


Article DOI: 10.1016/j.bmcl.2012.01.004
BindingDB Entry DOI: 10.7270/Q2C24WWN
More data for this
Ligand-Target Pair